Latest Blogs

बेडसोर्स क्या हैं? बेडसोर्स ऐसे घाव होते हैं जो त्वचा और उसके नीचे के ऊतकों को प्रभावित करते हैं, जब लंबे समय तक त्वचा पर दबाव पड़ता है। यह समस्या खासकर उन लोगों में होती है जो बिस्तर पर लेटे रहते हैं या जिनकी शारीरिक गतिविधि सीमित होती है, जैसे व्हीलचेयर पर बैठे व्यक्ति। बेडसोर्स आमतौर पर उन स्थानों पर विकसित होते हैं, जहां हड्डियां त्वचा के पास होती हैं, जैसे एड़ियां, टखने, कूल्हे, पीठ का निचला हिस्सा (टेलबोन) और कंधे के ब्लेड। बेडसोर्स के अन्य नाम क्या हैं? बेडसोर्स को प्रेशर सोर्स, डेकोबिटस अल्सर या प्रेशर अल्सर भी कहा जाता है। बेडसोर्स कितने सामान्य हैं? बेडसोर्स आमतौर पर उन लोगों में होते हैं जो बिस्तर पर लेटे रहते हैं या जिनकी शारीरिक गतिविधि सीमित होती है, खासकर अस्पतालों और नर्सिंग होम्स में। यह एक गंभीर स्वास्थ्य समस्या है जो विभिन्न प्रकार की देखभाल सुविधाओं, जैसे बड़े अस्पतालों, दीर्घकालिक देखभाल केंद्रों और रेजिडेंशियल केयर सुविधाओं में मरीजों को प्रभावित कर सकती है। बेडसोर्स के कारण अस्पताल में लंबी भर्ती की आवश्यकता हो सकती है, जिससे उपचार महंगा और समय-साध्य हो जाता है। बेडसोर्स आपके शरीर के किन हिस्सों को प्रभावित करते हैं? बेडसोर्स आमतौर पर उन हिस्सों पर होते हैं जो वजन उठाते हैं या निष्क्रियता के दौरान दबाव में रहते हैं, जैसे पीठ, नितंब, कूल्हे, एड़ियां, कोहनी और अन्य क्षेत्रों। ये स्थान बेडसोर्स के प्रति अधिक संवेदनशील होते हैं क्योंकि यहां रक्त संचार कम हो सकता है, और लंबे समय तक दबाव पड़ने से ऊतक क्षतिग्रस्त हो सकते हैं। बेडसोर्स से बचाव के लिए सही बॉडी पोजिशनिंग, नियमित शारीरिक गतिविधि और अच्छी त्वचा देखभाल आवश्यक हैं। बेडसोर्स के कारण क्या होते हैं? बेडसोर्स का मुख्य कारण त्वचा पर लंबे समय तक दबाव पड़ना है, जिससे उस क्षेत्र में रक्त प्रवाह कम हो जाता है। इसके परिणामस्वरूप, त्वचा की कोशिकाएं मरने लगती हैं, जो बेडसोर्स का कारण बनती हैं। बेडसोर्स के कुछ प्रमुख कारण निम्नलिखित हैं: लगातार दबाव: जब त्वचा पर दबाव पड़ता है, तो रक्त प्रवाह बाधित हो जाता है, जिससे त्वचा को आवश्यक ऑक्सीजन और पोषक तत्व नहीं मिल पाते। इसके कारण त्वचा कमजोर हो जाती है और कोशिकाएं मरने लगती हैं, जिससे बेडसोर्स विकसित हो सकते हैं। घर्षण (फ्रिक्शन): कपड़ों या बिस्तर से त्वचा की रगड़ने के कारण त्वचा की बाहरी परत में नुकसान हो सकता है, जिससे संवेदनशील त्वचा पर घाव बन सकते हैं और बेडसोर्स का खतरा बढ़ सकता है। शियर: जब त्वचा पर खिंचाव या खींचाव पड़ता है, खासकर गतिविधियों के दौरान, तो यह त्वचा को और अधिक नुकसान पहुंचा सकता है और बेडसोर्स के जोखिम को बढ़ा सकता है। कौन लोग बेडसोर्स के लिए अधिक जोखिम में हैं? जो लोग बिस्तर पर पड़े रहते हैं, व्हीलचेयर में होते हैं या जिनकी गतिविधि सीमित होती है, वे बेडसोर्स के प्रति अधिक संवेदनशील होते हैं। इसके अलावा, बुजुर्ग, संवेदी या न्यूरोलॉजिकल इंपेयरमेंट वाले लोग और जिनकी रक्त परिसंचरण में कमी होती है, वे भी बेडसोर्स के प्रति अधिक संवेदनशील होते हैं। कौन सी स्वास्थ्य स्थितियां आपके बेडसोर्स के जोखिम को बढ़ाती हैं? पैरालिसिस, डायबिटीज, वास्कुलर डिजीज (रक्तवाहिनियों से संबंधित रोग), और स्पाइनल कॉर्ड इंजरी जैसी स्वास्थ्य स्थितियां बेडसोर्स के जोखिम को बढ़ा देती हैं। इसके अतिरिक्त, खराब पोषण, निर्जलीकरण, और त्वचा व ऊतकों पर लंबे समय तक दबाव पड़ने से प्रेशर अल्सर या बेडसोर्स के विकास की संभावना और भी बढ़ जाती है। बेडसोर्स के लक्षण क्या हैं? लक्षणों में त्वचा का रंग या बनावट में बदलाव, सूजन, और संवेदनशील क्षेत्रों में दर्द शामिल हो सकता है। शरीर के हड्डी से जुड़े हिस्सों की इन लक्षणों के लिए नियमित जांच करना अत्यंत महत्वपूर्ण है। अगर शुरुआती चरण में पहचान कर ली जाए, तो बेडसोर्स का प्रभावी इलाज किया जा सकता है। बेडसोर्स के चरण क्या हैं? बेडसोर्स की गंभीरता के आधार पर, इन्हें चार चरणों में वर्गीकृत किया जाता है, जो उपचार की दिशा और प्रगति को पहचानने में मदद करते हैं: चरण I: यह सबसे हल्का चरण होता है। यहां, बेडसोर्स केवल त्वचा की ऊपरी परत को प्रभावित करता है जिससे त्वचा लाल और गर्म दिखाई देती है, और असुविधा या खुजली हो सकती है। चरण II: जब घाव त्वचा की सतह के नीचे गहरा हो जाता है। इससे त्वचा फट जाती है और यह एक फफोले या घर्षण जैसा दिखाई दे सकता है। चरण III: इस चरण में, घाव त्वचा की दूसरी परत में प्रवेश कर जाता है और वसा ऊतक तक फैल सकता है। इससे त्वचा के नीचे के ऊतकों में एक गड्ढा बन जाता है। चरण IV: ये घाव सबसे गंभीर होते हैं। इनमें से कुछ इतने गहरे होते हैं कि यह मांसपेशियों, लिगामेंट्स और हड्डियों को प्रभावित करते हैं। इन चरणों के अलावा, कभी-कभी बेडसोर्स को ऐसा रूप भी मिल सकता है जिसे स्टेज नहीं किया जा सकता, या फिर यह गहरे ऊतकों में हुए संदिग्ध नुकसान के रूप में दिखाई दे सकता है। बेडसोर्स के जटिलताएं क्या हैं? अगर बेडसोर्स का समय पर इलाज न किया जाए, तो इससे गंभीर जटिलताएं हो सकती हैं, जैसे त्वचा संक्रमण, सेप्सिस (रक्त विषाक्तता) और गंभीर संक्रमण के कारण अंगों का कटना (एम्प्यूटेशन)। अत्यधिक मामलों में, यह कैंसर का कारण भी बन सकता है। इसके अलावा, जानलेवा बैक्टीरियल संक्रमण, जैसे सेल्युलाइटिस और सेप्सिस का जोखिम भी बढ़ सकता है। संक्रमित बेडसोर्स के लक्षण क्या हैं? संक्रमित बेडसोर्स में सूजन, घाव के आसपास गर्मी, दुर्गंध या मवाद जैसी समस्याएं देखी जा सकती हैं। यदि किसी बेडसोर्स में संक्रमण के लक्षण नजर आएं, तो तुरंत चिकित्सा सहायता प्राप्त करना आवश्यक है। बेडसोर्स का निदान कैसे किया जाता है? बेडसोर्स का निदान एक विस्तृत शारीरिक परीक्षा से शुरू होता है। इस दौरान, आपका डॉक्टर आपसे घाव के उभरने का समय और उसके दर्दनाक होने के बारे में सवाल पूछ सकता है, ताकि यह निर्धारित किया जा सके कि आपको बेडसोर्स है या नहीं, और यदि है, तो वह किस चरण में है। अगर संक्रमण का संदेह हो, तो रक्त परीक्षण, बायोप्सी या इमेजिंग जैसे आगे के परीक्षण किए जा सकते हैं। बेडसोर्स के नॉनसर्जिकल उपचार क्या हैं? बेडसोर्स के नॉनसर्जिकल उपचार का ध्यान दबाव को कम करने, घाव को ठीक करने और संक्रमण को रोकने पर केंद्रित होता है। इसमें नियमित रूप से शरीर की स्थिति बदलना, विशेष कुशन या गद्दे का उपयोग करके वजन को समान रूप से वितरित करना और त्वचा को साफ और सूखा रखना शामिल है। ड्रेसिंग और टॉपिकल उपचार जैसे एंटीबायोटिक्स या दवाइयां बेडसोर्स के घावों को प्रबंधित करने और संक्रमण को रोकने में मदद कर सकते हैं। इसके अतिरिक्त, प्रोटीन और विटामिन से भरपूर संतुलित आहार के साथ पोषण में सुधार करने से ऊतक की मरम्मत में मदद मिलती है। फिजिकल थेरेपी गतिशीलता और परिसंचरण बनाए रखने में मदद करती है, जो बेडसोर्स की रोकथाम के लिए महत्वपूर्ण है। बेडसोर्स के इलाज के लिए कौन सी दवाएं उपयोग की जाती हैं? बेडसोर्स के कारण होने वाले दर्द से राहत पाने के लिए नॉनस्टेरॉयडल एंटी-इंफ्लेमेटरी ड्रग्स का उपयोग किया जा सकता है। इनमें इबुप्रोफेन या नेप्रोक्सेन सोडियम जैसी दवाएं शामिल होती हैं। स्थिति बदलने या घावों को साफ करने से पहले इनका उपयोग करने से असुविधा को कम करने में मदद मिलती है। अगर बेडसोर्स में संक्रमण हो गया है, तो एंटीबायोटिक्स की आवश्यकता हो सकती है। बेडसोर्स के सर्जिकल उपचार क्या हैं? बेडसोर्स के गंभीर मामलों, खासकर चरण IV में, तुरंत चिकित्सा देखभाल की आवश्यकता होती है, और ऐसी स्थिति में सर्जिकल हस्तक्षेप की आवश्यकता हो सकती है। एक सामान्य सर्जिकल उपचार त्वचा ग्राफ्टिंग है, जिसमें शरीर के किसी अन्य हिस्से से त्वचा या मांसपेशी का टुकड़ा घाव को ढकने के लिए प्रत्यारोपित किया जाता है। बेडसोर्स से बचाव कैसे किया जा सकता है? बेडसोर्स से बचाव के लिए कमजोर क्षेत्रों पर दबाव को कम करने और त्वचा के स्वास्थ्य को बनाए रखने के लिए सक्रिय उपायों को अपनाना जरूरी होता है। अपने शरीर की स्थिति को नियमित रूप से बदलना और विशेष कुशन या गद्दे का उपयोग करना दबाव बिंदुओं को कम करने में मदद करता है, जो बेडसोर्स से बचाव के लिए बेहद महत्वपूर्ण है। त्वचा को साफ और मॉइस्चराइज रखना सूखापन और जलन को रोकता है, जो त्वचा के टूटने का कारण बन सकता है। परिसंचरण और मांसपेशियों की टोन को बनाए रखने के लिए गतिहीन व्यक्तियों को गतिविधि और व्यायाम के लिए प्रोत्साहित करना आवश्यक है। पोषण और जलयोजन का ध्यान रखने से त्वचा की अखंडता बनाए रखने में मदद मिलती है, जिससे बेडसोर्स की रोकथाम में भी सहारा मिलता है। स्वास्थ्य सेवा प्रदाताओं द्वारा नियमित मूल्यांकन त्वचा की क्षति के प्रारंभिक लक्षणों की पहचान करने में मदद कर सकता है, जिससे समय पर हस्तक्षेप, जैसे ड्रेसिंग बदलना या पोजिशनिंग में समायोजन, किया जा सकता है। इस प्रकार, बेडसोर्स के विकास या बिगड़ने को रोका जा सकता है। बेडसोर्स वाले व्यक्ति के लिए भविष्य क्या है? ज्यादातर लोग समय पर पहचान और उपचार के साथ बेडसोर्स से पूरी तरह ठीक हो सकते हैं। हालांकि, जो लोग जोखिम में हैं, उन्हें गंभीर पुनरावृत्ति को रोकने के लिए सतर्क रहना चाहिए। डॉक्टर को कब देखना चाहिए? अगर आप बेडसोर्स के लक्षण महसूस करते हैं, जैसे कि लाल या बदरंग त्वचा जो छूने पर हल्की नहीं होती, खासकर यदि आप बिस्तर पर लेटे होते हैं या व्हीलचेयर पर हैं, तो आपको तुरंत अपने स्वास्थ्य सेवा प्रदाता से सलाह लेनी चाहिए। बेडसोर्स के दौरान पौष्टिक आहार का क्या महत्व है? एक पौष्टिक आहार समग्र स्वास्थ्य को बढ़ावा देता है और बेडसोर्स की तेजी से उपचार में मदद करता है। अपने आहार में प्रोटीन, विटामिन ए और सी, आयरन और जिंक जैसे खनिजों से भरपूर खाद्य पदार्थ शामिल करें। निष्कर्ष: बेडसोर्स को समझना, उनके कारणों को जानना और उपचार विकल्पों के बारे में जानकारी होना इन्हें प्रभावी रूप से रोकने और प्रबंधित करने के लिए महत्वपूर्ण है। नियमित रूप से स्थिति बदलना, अच्छी त्वचा देखभाल, पौष्टिक आहार और पेशेवर चिकित्सा सलाह इस स्वास्थ्य स्थिति के प्रबंधन में मदद करने वाले प्रमुख तत्व हैं। मेट्रोपोलिस हेल्थकेयर विभिन्न परीक्षणों के लिए घर पर सैंपल कलेक्शन सहित विश्वसनीय डायग्नोस्टिक सेवाएं प्रदान करता है। रिपोर्ट्स को सुविधाजनक तरीके से ईमेल या मेट्रोपोलिस ट्रूहेल्थ ऐप के माध्यम से ऑनलाइन साझा किया जाता है। मेट्रोपोलिस हेल्थकेयर की विशेषज्ञता और मरीज-केंद्रित दृष्टिकोण मरीजों को अपनी सेहत को प्राथमिकता देने के लिए सशक्त बनाता है।

What is galactorrhea? Galactorrhea is a condition characterised by the production of milk or a milky nipple discharge in individuals who are not pregnant or breastfeeding. The discharge can be from one or both breasts and may be constant or intermittent. It's important to note that galactorrhea is not a disease itself but rather a symptom of an underlying condition that needs to be identified and addressed. Who does it affect? Galactorrhea can affect women, men, and even newborn babies. It is most common in women, including those who have never had children or who have gone through menopause. In men, galactorrhea is often associated with hormonal imbalances, such as testosterone deficiency. Newborns can also experience temporary galactorrhea, known as "witch's milk," due to exposure to high maternal estrogen levels during pregnancy. How common is galactorrhea? While the exact prevalence of galactorrhea is not well-documented, it is considered relatively rare. However, it can occur in up to 5% of neonates as "witch's milk." What are the causes of galactorrhea? Galactorrhea causes are often related to increased levels of prolactin, a hormone produced by the pituitary gland that stimulates milk production. Some common galactorrhea causes include: Medications: Certain drugs, such as sedatives, antidepressants, antipsychotics, high blood pressure medications, and opioids, can increase prolactin levels. Pituitary gland issues: Pituitary tumours (prolactinomas), non-prolactin-secreting pituitary tumours, and infiltrative disorders of the pituitary stalk/hypothalamus can lead to hyperprolactinemia. Systemic diseases: Conditions like hypothyroidism, chronic kidney disease, spinal cord injury, and an underactive thyroid can contribute to galactorrhea. Hormonal imbalances: High estrogen levels, as seen in pregnancy or ovarian hyperstimulation syndrome, can also cause galactorrhea. Physical stimulation: Excessive breast stimulation, such as during sexual activity, can trigger galactorrhea. Idiopathic galactorrhea: In some cases, the cause of galactorrhea cannot be determined, and it is termed idiopathic galactorrhea. What are the symptoms of galactorrhea? The primary symptom of galactorrhea is a milky nipple discharge that may be constant or intermittent and can occur from one or both breasts. The discharge may be spontaneous or manually expressed. Other galactorrhea symptoms in women can include absent or irregular menstrual periods. If a pituitary tumour is present, headaches or vision problems may also occur. Is galactorrhea life-threatening? While galactorrhea itself is not life-threatening, it can be a sign of an underlying condition that may require medical attention. For example, pituitary tumours or systemic diseases need to be addressed to prevent complications. If you experience persistent galactorrhea symptoms, it's important to consult a healthcare professional for proper diagnosis and treatment. Does galactorrhea cause weight gain? Galactorrhea does not directly cause weight gain. However, some underlying conditions that lead to galactorrhea, such as hypothyroidism or certain medications, may contribute to weight changes. Is galactorrhea actually milk? Yes, the discharge produced in galactorrhea is milk or a milky substance from the breast. The presence of milk can be confirmed through a Sudan IV stain for fat droplets. However, it's important to note that galactorrhea is not the same as the normal milk production that occurs during pregnancy and breastfeeding. Can newborn babies get galactorrhea? Yes, newborn babies can experience temporary galactorrhea, known as "witch's milk," due to exposure to high maternal estrogen levels during pregnancy. This condition usually resolves on its own within a few weeks after birth and does not require treatment. Can men get galactorrhea? Although less common than in women, men can indeed experience galactorrhea. In men, galactorrhea is often associated with testosterone deficiency (male hypogonadism), which can also lead to breast enlargement (gynecomastia), erectile dysfunction, and a lack of sexual desire. How is galactorrhea diagnosed? Diagnosing galactorrhea involves several steps: Medical history: Your doctor will take a detailed history of your medications, symptoms, and menstrual irregularities (in women). Physical examination: A thorough examination of the breasts will be performed to check for masses or other abnormalities. Laboratory tests: Blood tests to measure prolactin and thyroid-stimulating hormone (TSH) levels may be ordered. Imaging: If a pituitary lesion is suspected, an MRI of the head may be recommended. Mammography, ultrasonography, or ductography may be performed if breast abnormalities are suspected. How is galactorrhea treated? Galactorrhea treatment focuses on addressing the underlying cause. If medications are contributing, your doctor may suggest discontinuing or adjusting them. For cases linked to conditions like hypothyroidism, hormone replacement may be prescribed to restore balance. If a pituitary tumour is identified, options may include medication such as bromocriptine or cabergoline to lower prolactin levels. In cases where medication isn't effective or if the tumour is large, surgery may be recommended to remove it. Lifestyle changes, like reducing stress and avoiding breast stimulation, may also help reduce symptoms. Your healthcare provider will create a galactorrhea treatment plan personalised to your condition, considering factors like the severity of symptoms and overall health. Regular follow-ups are essential to monitor progress and adjust treatment if necessary, ensuring the most effective management of galactorrhea. What complications are associated with galactorrhea? While galactorrhea itself is not harmful, it can be a sign of underlying conditions that may lead to complications if left untreated. These can include: Pituitary tumours, which can cause headaches, vision problems, and hormonal imbalances Osteoporosis, if hyperprolactinemia is prolonged and untreated Infertility, as high prolactin levels can interfere with ovulation in women and testosterone production in men How long can galactorrhea last? The duration of galactorrhea varies depending on the underlying cause. In some cases, such as with medication-induced galactorrhea, the condition may resolve once the offending drug is discontinued. However, if galactorrhea is caused by a pituitary tumour or other chronic condition, it may persist until the underlying issue is effectively treated. Can galactorrhea be prevented? Preventing galactorrhea isn’t always possible, but you can reduce risk by informing your doctor of medications, attending regular check-ups to monitor hormonal health, and avoiding excessive breast stimulation. Discuss preventive options with your healthcare provider if at risk. What are the risk factors for galactorrhea? Risk factors for galactorrhea include certain medications, pituitary disorders, hormonal imbalances, breast surgery, chest radiation, and excessive breast stimulation. Recognising these can help you monitor your health and seek timely care. What is the outlook for people with galactorrhea? The outlook for people with galactorrhea depends on the underlying cause. In many cases, galactorrhea can be effectively managed or resolved with appropriate treatment. However, it's important to note that some causes of galactorrhea, such as idiopathic galactorrhea, may not have a specific treatment. In these cases, symptom management and regular monitoring may be recommended. When to see a doctor? If you experience any of the following, it's important to consult a healthcare professional: Persistent or bothersome milky nipple discharge Nipple discharge that is bloody or clear Breast pain, lumps, or changes in breast shape or size Headaches or vision problems Irregular menstrual periods or difficulty getting pregnant Conclusion Galactorrhea can be a confusing and concerning condition, but with the right information and medical guidance, it can be effectively managed. Remember, if you experience any unusual breast discharge or related symptoms, don't hesitate to consult a healthcare professional for personalised advice and care. At Metropolis Healthcare, we understand the importance of accurate diagnosis and personalised treatment plans. Our team of highly skilled pathologists and state-of-the-art diagnostic facilities, including home services, are here to support you on your journey to better health.

Introduction Imagine your stomach as a strong castle, surrounded by a protective barrier that defends against the ongoing assault of acids and enzymes. This barrier, called the stomach lining or mucosa, can sometimes face serious attacks, leading to inflammation which known as gastritis. When gastritis occurs, it’s like the castle’s guard is in danger! This inflammation can result from infections, specific foods, or stomach chemicals. Gastritis is a common medical term you might have heard but might not fully understand. It’s natural to feel concerned about health issues, but knowing what gastritis is and how it affects your body can help you manage it better. This article aims to demystify the topic of gastritis, breaking down its types, symptoms, causes, and treatment options, and guide you through its management for better digestive health in a simple and understandable language. What is Gastritis? Gastritis is a common health concern involving inflammation of the stomach lining, or 'mucosa'. This protective layer guards the stomach from acids and enzymes. When the mucosa gets irritated or damaged, inflammation occurs as a response from the immune system, resulting in gastritis. This uncomfortable condition can be caused due to various factors, including infections and certain medications. Gastritis is a common problem for many people globally. It often leads to discomfort that can interfere with everyday activities. But what exactly is gastritis, and how can you manage and treat it effectively? Gastritis refers to inflammation or swelling of the stomach lining. This lining serves as a shield against digestive acids, enzymes, and microorganisms that pass through the stomach daily. When this lining gets irritated for various reasons, gastritis develops, leading to discomfort that can disrupt your everyday life. What are the different Types of Gastritis? Understanding the types of gastritis helps in its management. It can broadly be classified into two categories: acute and chronic gastritis. Acute Gastritis: This type occurs suddenly and can lasts for a short period. The causes of acute gastritis are typically temporary as well. Chronic Gastritis: This type is more long-lasting but may not always be noticeable. It develops gradually due to persistent conditions like infections or prolonged intake of certain medications. Within these two categories, gastritis may further be erosive or non-erosive: Erosive Gastritis: This type occurs when factors like acid, bile, alcohol, or certain medications damage the stomach lining, leading to painful ulcers. Nonerosive Gastritis: This type doesn’t cause erosions but can irritate the stomach lining, resulting in redness. One specific form is atrophic gastritis, which can lead to digestive problems by thinning or wasting away the stomach lining. Specific types of gastritis are labelled according to their causes, such as infectious gastritis or autoimmune gastritis. How Common is Gastritis? If you're thinking you're the only one struggling with this condition, think again! Gastritis is actually quite common. In the US, around 8 in every 1,000 people are affected by acute gastritis, which is often linked to short-term infections, alcohol, and medications. Chronic gastritis affects about 2 out of every 10,000 people in the US. But worldwide, almost half of the population has chronic gastritis linked with a widespread bacterial infection called H. pylori. Globally, as much as half the population suffers from chronic gastritis linked to a widespread bacterial infection known as H. pylori. What are the Symptoms of Gastritis? Identifying gastritis symptoms can be challenging as it may not always cause noticeable symptoms. However, when the stomach lining can no longer protect itself from acids and enzymes, you might experience symptoms such as: Loss of appetite or feeling full soon after eating Stomach pain and bloating Nausea and/or vomiting If you have a bleeding ulcer due to erosive gastritis, symptoms may include: Black blood in your stool (melena) Black blood in your vomit (coffee ground emesis) Recognizing these symptoms is important for seeking timely medical attention, as early diagnosis and treatment can help manage the condition effectively. How do you recognise Gastritis Pain? Gastritis pain is usually felt in the upper middle abdomen or the "epigastric "region. The inflammation causes general discomfort in this area. If an ulcer develops due to erosive gastritis, you might experience a more localised burning or a gnawing pain which often improves after eating. Gastritis pain typically occurs in the upper middle abdomen. This pain can be difficult to pinpoint but is generally characterised by a burning or gnawing sensation, which might feel better after eating. What Causes Gastritis? The inflammation caused by gastritis is generally a response to threats to your stomach lining. These can include infections and substances you take in: Infections: Both bacterial and viral infections can lead to short-term acute gastritis. Additionally, chronic gastritis can develop from a prolonged infection with H. pylori. Chemicals: Alcohol and some drugs can cause either acute or chronic gastritis by chemically eroding the stomach lining (erosive gastritis). One of the most common causes of gastritis is the overuse of NSAIDs (nonsteroidal anti-inflammatory drugs), like aspirin and ibuprofen. Certain recreational drugs particularly cocaine, can also contribute to developing this condition. Autoimmune Disease: Chronic autoimmune gastritis can occur spontaneously or as a side effect of another autoimmune condition. Reduced Blood Supply: Major surgery, trauma, or critical illness can cause acute gastritis. Severe physiological stress can make your stomach lining more vulnerable to digestive chemicals. Additional Causes: These include radiation therapy, chemotherapy, bile reflux, etc. Reduced Blood Supply: Major surgery, trauma, or critical illness can lead to acute gastritis. Reduced Blood Supply: Major surgery, trauma, or critical illness can lead to acute gastritis by decreasing blood flow to the stomach lining. This decreased blood flow makes the stomach more vulnerable to damage from acids and enzymes. Stress: Severe physiological stress can make the stomach lining more vulnerable to damage from digestive chemicals. Additional Causes: Other factors include radiation therapy, chemotherapy, and bile reflux, among others. What are the Complications of Gastritis? While gastritis is typically temporary and not serious, if left untreated for an extended period can damage your stomach lining and result in complications. Erosive Gastritis and Ulcer Complications: Frequent ulcers caused by an erosive gastritis can lead to gastrointestinal bleeding and anaemia. Scar tissue in stomach can block the openings at the bottom (pylorus), causing gastric outlet obstruction (GOO). Non-Erosive Gastritis, Atrophy and Metaplasia: A long-term non-erosive gastritis can result in thinning of your stomach mucosa (atrophy) and impairing digestion as well as and absorption of certain nutrients. In rare cases, it can cause the cells in your stomach lining to transform into a different type of tissue (gastric intestinal metaplasia), which is considered a precancerous condition. How is Gastritis Diagnosed? While a healthcare provider might suspect gastritis based on symptoms, its confirmation usually requires a biopsy taken during an upper endoscopy exam. Additional tests might include blood tests, stool tests, and H. pylori breath tests. Healthcare providers diagnose gastritis through imaging tests like the upper GI series or biopsy performed during upper endoscopy exam. Diagnosis of gastritis often begins with a healthcare provider checking your symptoms and reviewing your health history. Imaging tests such as an upper GI series can detect ulcers or erosion in your stomach lining. To confirm gastritis, a tissue sample (biopsy) is typically taken during an upper endoscopy exam. Does Gastritis go away by Itself? Yes, acute gastritis often resolves spontaneously once the root cause is addressed. In contrast, chronic gastritis necessitates professional treatment for proper management. Acute gastritis typically clears up after the triggering factor is addressed, while chronic gastritis needs treatment for resolution, as it is associated with other long-term health issues. How Can I Relieve Gastritis Fast? Over-the-counter medications can help soothe irritation and neutralises stomach acid for temporary relief. However, it's important to consult to a healthcare provider for long-term care. While options like proton pump inhibitors (PPIs) can provide temporary relief from gastritis symptoms, getting professional advice is still important, even if you're treating yourself. How Do You Cure Gastritis Permanently? The most effective gastritis treatment depends on its cause and requires professional care. It might involve: Antibiotics and other medications for H. pylori Switching from NSAIDs if they are causing gastritis Addiction treatment services for substance abuse Targeted drugs for autoimmune diseases Rarely, surgery to fix gastrointestinal (GI) bleeding, ischemia or bile reflux Permanent relief from chronic gastritis necessitates professional care that addresses the underlying cause. These include antibiotics for H. pylori infections, opting to alternative medications if NSAIDs are the culprit, or seeking addiction treatment for issues like alcohol use disorder or cocaine addiction. Is Gastritis Contagious? While gastritis isn't contagious, the infections causing it, like H. pylori, are. Good hygiene practices like handwashing can help prevent the spread of such infections. While gastritis itself isn't contagious, infections like H. pylori that cause it are contagious and spread via the fecal-to-oral route. What is the Outlook for this Condition? In most cases, gastritis improves quickly with treatment. However, for some individuals, recovery may also involve permanent lifestyle changes, like quitting smoking or alcohol. While most cases of gastritis respond well to treatment, lasting recovery may necessitate ongoing lifestyle adjustments and management of underlying chronic conditions. Conclusion Gastritis can be challenging, but understanding its symptoms, causes, and its treatment options can help you take charge of your health. Managing gastritis effectively is crucial for better digestive health. With the right information and support from your healthcare provider, you can navigate this condition successfully. Understanding and managing this condition can be vital for better digestive health. Regular health check-ups and blood tests are important, as they can identify underlying issues that may lead to gastritis. Metropolis Healthcare is always here to assist you with our comprehensive diagnostic and pathology services. Our dedicated professionals strive provide accurate test results to help you manage gastritis more effectively. Their commitment to reliable results and personalized care empowers you to take control of your health. So don’t wait, prioritise your health today with the right steps and support from Metropolis Healthcare. Let’s work towards better digestive health together!

Squamous cell carcinoma is a common skin cancer that comes with a variety of symptoms and treatment options. More often people feel anxious upon hearing the term squamous cell carcinoma, but understanding what it includes, how it can present, its causes, and the potential treatments can ease those worries. This article aims to clarify squamous cell carcinoma and boost your understanding of this health condition, allowing you to feel more informed and at ease. By gaining insight into it, you can significantly lessen any anxiety related to the diagnosis and treatment processes. What is Squamous Cell Carcinoma? Squamous cell carcinoma is a common type of skin cancer. It originates in the squamous cells that form the middle and outer layers of your skin. While squamous cell carcinoma generally not a life-threatening, if left untreated, it can grow large or can spread to other areas of the body, causing serious complications. Early detection is essential because identifying it in its initial stages can help to prevent serious complications. However, if untreated, this type of cancer can result in significant health risks and complicate treatment options for patients in the long run. What are the Types of Squamous Cell Carcinoma? Squamous cell carcinoma primarily affects the skin, but it can also develop in other tissues containing squamous cells, such as the lungs, mouth, and tongue. The most common types include: Cutaneous Squamous Cell Carcinoma (cSCC): This type develops on the skin and is frequently linked to prolonged exposure to UV radiation. Lung Squamous Cell Carcinoma: This type develops in the lining of the bronchial tubes in the lungs. Oral Squamous Cell Carcinoma: This occurs inside the mouth, often appearing as a persistent sore or rough patch. Squamous Cell Carcinoma of the Tongue: This subtype specifically manifests on the tongue, often causing concerning symptoms. Each type of SCC presents unique symptoms and necessitates specific diagnostic methods and treatment plans. Who does Squamous Cell Carcinoma Affect? Squamous cell carcinoma can affect anyone, regardless of their age, gender, or ethnicity. However, people with lower levels of melanin in their skin might be at a higher risk of developing this condition. Melanin is what gives the skin its color and helps protect it from harmful ultraviolet (UV) radiation. Due to this, individuals with Black or brown skin, who have more melanin, are usually are less susceptible to this type of cancer compared to those with lighter skin. Squamous cell carcinoma is commonly found in individuals with light-colored eyes, blond or red hair, and skin that burns easily in the sun. Having a history of sunburns, particularly those that lead to blisters during childhood or adolescence, can significantly raise the risk. Furthermore, individuals with weakened immune systems due to medical conditions like leukemia or , or those undergoing immunosuppressive treatments after organ transplants, also face a higher risk of developing squamous cell carcinoma as time goes on. How Common is Squamous Cell Carcinoma? Squamous Cell Carcinoma (SCC) is a common type of cancer in India, occurring as both skin and oral cancer. It represents about 20% of all the skin cancer cases. The chances of developing SCC can vary based on factors like age, gender, and exposure to risks such as UV radiation from the sun and tobacco smoke. In oral cancer, Squamous Cell Carcinoma (SCC) makes up 90% of cases, with India having over 100,000 new cases each year, the highest in the world. Important risk factors consist of using tobacco, drinking alcohol, diet, HPV infection, genetics, and oral hygiene. Early detection through regular self-examinations is very important for successful treatment. What are the Symptoms of Squamous Cell Carcinoma? The squamous cell carcinoma symptoms differ depending on which part of the body it affects. However, a few common signs include: A bump that can vary in size from a pea to a chestnut, often with a rough or scaly surface, resembling a wart. A sore that doesn't heal or reappears after healing. A flat, reddish, scaly patch larger than 1 inch (2.5 centimeters). A new sore or raised area on an old scar, a rough patch on the lip that turns into an open sore, or a sore or rough patch inside the mouth. It's crucial to consult a healthcare provider if you experience any of these symptoms. Where on my Body can I get Squamous Cell Carcinoma? Squamous cell carcinoma can develop anywhere on your body, including areas that that aren't exposed to sunlight. While this cancer most commonly occurs on sun-exposed skin such as the scalp, backs of hands, ears, and lips. But it can also happen inside your mouth, on the soles of your feet, on your genitals, or in other areas of your body. What Causes Squamous Cell Carcinoma? The main cause of squamous cell carcinoma is too much exposure to UV radiation, which can come from sunlight or tanning beds. This radiation is found in sunlight and also from artificial sources like tanning beds and lamps. When UV radiation affects your skin cells, it causes changes in their DNA that can lead to squamous cell carcinoma. Besides UV exposure, other factors like having a weak immune system can also play a role in developing this condition. Does Squamous Cell Carcinoma Spread? Yes, if left untreated, squamous cell carcinoma can spread to nearby lymph nodes or other organs. If it infiltrates in deeper tissues or mucous membranes (like lips), the survival rate may reduce because due to the potential complications. The cancer cells can break away and move to other parts of the body, leading to serious problems. However, finding and treating the cancer early greatly lowers the risk of this happening. How is Squamous Cell Carcinoma Diagnosed? Doctors typically perform a physical examination, take a biopsy (sample of suspicious skin) for lab testing, and ask for a detailed medical history. A biopsy usually involves removing a small piece of the affected skin and sending it to a laboratory for analysis. What tests diagnose squamous cell carcinoma? Diagnosing squamous cell carcinoma involves several important tests that help determine the presence and extent of the cancer. Skin exam: The doctor checks for abnormal moles or pigmented areas. Biopsy: A tissue sample is taken for lab analysis, with types including shave, punch, incisional, and excisional. Blood test: A complete blood count (CBC) is commonly used to assist in diagnosis. Imaging tests: CT scans or MRIs assess the size of the carcinoma and check for spread. Lymph node biopsy: Nearby lymph nodes are removed to look for cancer signs. Nasopharyngolaryngoscopy: A flexible camera examines the throat through the nose. These diagnostic methods are crucial for identifying squamous cell carcinoma. Quick biopsy results can lead to effective treatment, and complete removal of the tumor may cure the cancer without further intervention. What are the Stages of Squamous Cell Carcinoma? Squamous cell carcinoma (SCC) has four stages that indicate how far the cancer has spread in the body: Stage 0: The cancer is only in the epidermis, the top layer of skin, also known as carcinoma in situ (CIS). Stage 1: The cancer has spread deeper into the skin but has not reached nearby lymph nodes or healthy tissues. Stage 2: The cancer has advanced further into the skin and may have affected lower layers or nerves, but it has not spread to lymph nodes or healthy tissues. Stage 4: The cancer has spread to at least one distant organ, such as the lungs, liver, brain, or other parts of the skin. Understanding the stage helps doctors determine the most effective treatment options. How is Squamous Cell Carcinoma Treated? The treatment for squamous cell carcinoma varies based on factors such as the cancer's severity and location. Mohs Micrographic Surgery: A precise technique that removes cancerous skin layer by layer. Excisional Surgery: Involves cutting out the cancer along with some surrounding healthy tissue. Electrosurgery: Uses electrical currents to destroy cancer cells. Cryosurgery: Freezes the cancer cells to eliminate them. Radiation: Targets cancer cells with high-energy rays. Photodynamic Therapy: Uses light-sensitive drugs activated by light to kill cancer cells. Systemic Drugs: Medications that affect the entire body, used in advanced cases. Each treatment option comes with potential side effects and risks, so it’s important to discuss these with your healthcare provider. Consult your doctor to determine the best treatment plan for your situation. What are the Side Effects of Squamous Cell Carcinoma Treatments? Each of the squamous cell carcinoma treatment has potential side effects, ranging from minor discomfort to more serious issues. Some common side effects include: Pain at the treatment site Scarring Changes in skin colour Fatigue (with radiation therapy) Discuss these potential side effects with your doctor before starting any treatment plan. How Can we Prevent Squamous Cell Carcinoma? Preventing squamous cell carcinoma primarily involves protecting your skin from the UV radiation. As well as avoiding excessive sun exposure, using sunscreen, wearing protective clothing, and not using tanning beds or lamps. What Can we Expect If we Have Squamous Cell Carcinoma? With an early detection and suitable treatment, the majority of individuals fully recover from squamous cell carcinoma. The survival rate is significantly high when the cancer is identified early. However, it's crucial to attend all the follow-up appointments with your doctor, as squamous cell carcinoma can recur. If detected early and treated quickly, the outlook for squamous cell carcinoma is usually very positive. Nonetheless, regular check-ups are important to avoid any recurrence or complications. When to See a Doctor? If you notice any unusual growths on your skin or experience symptoms of squamous cell carcinoma, get medical advice right away. Early detection is crucial for effective treatment and management. What is the Difference between Squamous Cell Carcinoma and Basal Cell Carcinoma? Both basal cell carcinoma and squamous cell carcinoma are types of skin cancer, but they develop in different cells. Basal cell carcinoma begins in the basal cells found in the lower layer of the skin. It is the most common type of skin cancer and is usually less aggressive than squamous cell carcinoma. In contrast, squamous cell carcinoma begins in the squamous cells of the outer layer of the skin and can spread more readily if not treated promptly. What is Squamous Cell Carcinoma in Situ? Squamous cell carcinoma in situ (Bowen's disease), is an early stage of squamous cell carcinoma. In this condition, the cancer cells are still confined to the upper layer of the skin and have not invaded deeper tissues. Although it is not invasive yet, early detection and treatment are crucial to stop it from developing into more serious types of skin cancer. Conclusion Understanding and recognising the symptoms of squamous cell carcinoma is crucial for timely diagnosis and treatment. By being informed, you can take charge of your health and act quickly. If you notice any unusual changes in your skin that don’t heal, or rough patches, it’s important to consult a healthcare provider right away. Early intervention can make a big difference in your outcome. At Metropolis Healthcare, we offer advanced diagnostic services, including blood testing for related markers. Our qualified technicians can conveniently collect samples from your home. Test reports are readily available online, making it easy for you to stay on top of your health and access your medical information conveniently. With accurate information and reliable healthcare services, prioritising your health becomes easy and achievable. So take that first step towards health awareness today!

What is a sebaceous cyst? Ever discovered a strange round bump beneath your skin surface that feels like a lump? This might be what health experts call an epidermal inclusion cyst or a sebaceous cyst. An epidermal inclusion cyst is a common and harmless skin bump that forms when skin cells pile up in one area under the dermis. These cysts are filled with a thick, keratin-like substance and can appear anywhere on the body, mostly found on the face, neck, and trunk. The name "sebaceous cyst" can be misleading as these cysts do not originate from sebaceous glands. Epidermal inclusion cysts can develop due to skin injuries, blockages in hair follicles, or congenital factors. While they are generally asymptomatic, they may become inflamed or infected, leading to discomfort. Treatment is often unnecessary unless the cyst becomes painful or bothersome; in such cases, healthcare providers may recommend drainage or surgical removal. Understanding the causes of epidermal inclusion cysts is essential for proper diagnosis and management, distinguishing them from other skin lesions. How common are epidermal inclusion cysts (sebaceous cysts)? You might be surprised to learn that epidermal inclusion cysts are the most common type of skin cyst. Because of this, it's normal to see one or know someone who has one. What does an epidermal inclusion cyst (sebaceous cyst) look like? An epidermal inclusion cyst appears as a round bump or dome-shaped lump on the skin. Since, sebaceous cyst symptoms may vary from person to person. Here's what you might notice: A dark dot in the centre of the cyst Skin discolouration around the area Tenderness or warmth when touched The size ranges from as small as 0.25 inches to more than 2 inches What are epidermal inclusion cysts (sebaceous cysts) filled with? Epidermal inclusion cysts are filled with thick, cheesy, malodorous substance consisting of keratin and cell debris, not sebum. These cysts are form when the epidermal cells grow in a small space in the dermis. Is an epidermal inclusion cyst (sebaceous cyst) painful? Most epidermal inclusion cysts aren't usually painful unless they become inflamed or rupture (break open). In such cases, you may experience symptoms like skin irritation, pain or itching at the site of the cyst. It's highly recommended to see your healthcare provider if you develop pain near the cyst or experience other concerning symptoms. Where do epidermal inclusion cysts (sebaceous cysts) form? Epidermal inclusion cysts can form anywhere on your body but are most frequently found in areas like: Face Chest Back Scalp Neck Legs Arms Genitalia These areas provide optimal conditions for cyst growth due to their high concentrations of hair follicles. What causes an epidermal inclusion cyst (sebaceous cyst)? An epidermal inclusion cyst, often incorrectly called a sebaceous cyst, forms when skin cells multiply in a small pocket under the skin instead of shedding naturally. These cysts can develop due to a blocked hair follicle or skin trauma, causing cells to build up and form a sac filled with keratin, a protein that makes up the skin, hair, and nails. Sebaceous cyst causes due to damage from cuts, surgical wounds, or conditions such as acne that block hair follicles. Certain genetic conditions, like Gardner’s syndrome or basal cell nevus syndrome, can also increase the risk of getting these cysts. Although they are usually harmless, an epidermal inclusion cyst can become inflamed or infected, leading to redness, swelling, and discomfort. Maintaining a good hygiene and skincare can help minimise sebaceous cyst causes. What are the risk factors for epidermal inclusion cysts (sebaceous cysts)? Although epidermal inclusion cysts can occur in anyone, certain factors increase your likelihood of developing them. These typically include: Age: They are more common among individuals between 20-60 years Gender: More prevalent in individuals assigned male at birth (AMAB) Genetic conditions: Rare genetic conditions such as Gardner syndrome and Gorlin syndrome Medications: Certain medications like BRAF inhibitors, Imiquimod etc may increase your risk Is an epidermal inclusion cyst (sebaceous cyst) contagious? Rest assured, epidermal inclusion cysts are not contagious and cannot be spread from one person to another What are the complications of an epidermal inclusion cyst (sebaceous cyst)? Epidermal inclusion cysts are usually harmless, but they can sometimes can lead to certain complications. Such as if the cyst gets inflamed or infected, leading to swelling, pain, and skin discoloration. If a cyst ruptures, it can also swell and leak its contents. In rare cases, malignancy (cancer) has been found in these cysts, including squamous cell carcinoma and basal cell carcinoma. If you notice a rapid cyst growth, significant pain or any other concerning changes in your cyst, it's crucial to consult your healthcare provider immediately. Is an epidermal inclusion cyst a sign of cancer? Epidermal inclusion cysts are usually benign and rarely harmful. However, in rare cases, malignancy or cancer can form within the cyst. It's important to consult your healthcare provider if you notice any changes with your skin or the cyst. How is an epidermal inclusion cyst (sebaceous cyst) diagnosed? Diagnosing an epidermal inclusion cyst (often called a sebaceous cyst) involves physical examination by a healthcare professional. The cyst usually looks like a small, round bump under the skin, often with a central opening or "punctum." It may feel firm and movable when pressed. To confirm the diagnosis, the doctor may ask about the cyst’s history, such as when it first appeared and any changes in size or symptoms like pain or discharge. In some cases, an ultrasound or MRI may be recommended to distinguish it from other types of growths. If the cyst appears unusual or shows signs of infection, the doctor may perform a biopsy to rule out other conditions. Proper diagnosis ensures the appropriate treatment plan. Should we see a specialist for an epidermal inclusion cyst? An epidermal inclusion cyst isn't usually painful unless it gets inflamed or ruptures. However, If you notice changes like rapid growth or signs of infection such as redness, swelling, or leaking fluid, it’s best to see a healthcare provider. They may refer you to a dermatologist if needed. How is an epidermal inclusion cyst (sebaceous cyst) treated? Epidermal inclusion cyst or sebaceous cyst treatment typically depends on its size and symptoms. Small, painless cysts may not require treatment and can be monitored. If the cyst is painful, infected, or cosmetically bothersome, it can be drained or injected with a corticosteroid to reduce inflammation. Surgical removal is an option for recurring or large cysts. Treatment for an epidermal inclusion cyst, also known as a sebaceous cyst, usually depends on its size and symptoms. Small, painless cysts may not need a treatment and can simply be monitored. If the cyst is painful, infected, or causes any cosmetic concerns, it can be drained or treated with a corticosteroid injection to reduce inflammation. Surgical removal is an option for larger or recurring cysts. Epidermal Inclusion Cyst (Sebaceous Cyst) Removal Epidermal inclusion cyst removal is usually done when the cyst is infected, painful, or cosmetically unappealing. The procedure is typically performed under local anesthesia in a doctor’s office. A small incision is made, and the cyst is carefully removed along with its entire sac to prevent prevent recurrence. If the cyst isn’t fully removed, it may regrow. For infected cysts, drainage or antibiotics may be needed before removal. The procedure is generally quick, with minimal discomfort and scarring. Proper aftercare, including keeping the area clean and following the doctor’s instructions, helps ensure a smooth healing process and reduces the risk of recurrence. Can sebaceous cysts be prevented? Preventing sebaceous cysts may not always be possible because they can develop due to factors like genetics or certain medications. However, maintaining good hygiene and skin health might reduce the risk of developing these cysts. What is the outlook for sebaceous cysts? Sebaceous cysts are typically benign and mostly cause discomfort or cosmetic concern rather than serious health issues. If surgically removed, they're less likely to return. Rarely, an infection could develop at the removal site, requiring antibiotic treatment. Does an epidermal inclusion cyst (sebaceous cyst) go away? While some sebaceous cysts may shrink or disappear over time, others can persist and grow in size. It's important to monitor any changes and seek medical advice if necessary. Can epidermal inclusion cysts get worse? If left untreated, epidermal inclusion cysts could potentially become infected or rupture, causing symptoms like inflammation and pain. In such cases, immediate medical attention is required. When to see a doctor? If you notice a new skin lump or changes in an existing one, like rapid growth, signs of infection, or increased pain, it's a good idea to see a healthcare professional right away. Is an epidermal inclusion cyst (sebaceous cyst) dangerous? While epidermal inclusion cysts are typically harmless, there have been rare cases where cancerous changes were found inside them. Therefore, it's important to have any changes in your skin, such as growth, pain, or unusual features, checked by a healthcare provider. Conclusion While epidermal inclusion cysts (often called sebaceous cysts) can be a bit concerning due to their appearance and any discomfort they may cause, they are usually harmless and treatable. Understanding what these cysts are and knowing when to seek medical advice is essential for managing them effectively. If you need a trusted partner in your healthcare journey or a reliable diagnostic provider for health check-ups, Metropolis Healthcare is here to help. With our advanced diagnostic labs and a qualified team of technicians offering at-home blood sample collection, we're dedicated to providing accurate results and personalized care right at your doorstep. After all, prioritising your health is an integral part of living a fulfilling life.

When it comes to maintaining health, knowledge is power. One such subject demanding our attention is uterine cancer. By identifying the symptoms, understanding its causes, and treatment choices can help you assist those affected or those who want to prevent this condition. This guide aims to clarify these topics to help improve health knowledge and overall well-being. What is uterine cancer? Uterine cancer refers to cancers that develop in the uterus, primarily divided into two types: endometrial cancer and uterine sarcoma. Endometrial cancer starts in the inner lining of the uterus and is the most common type, exhibiting symptoms like abnormal bleeding. Uterine sarcoma begins in the muscle wall of the uterus and is less common but can be more aggressive. Identifying these types are essential for an early detection and effective treatment, improving overall health outcomes. Are endometrial cancer and uterine cancer the same? While people often use “endometrial cancer” and “uterine cancer” interchangeably, it’s essential to clarify that they are not exactly the same. Endometrial cancer accounts for about 95% of all uterine cancers making it far more common than uterine sarcomas. What does the uterus do? The uterus plays a crucial role in a woman's reproductive system by providing a nurturing environment for a developing fetus during pregnancy. What does the endometrium do? The endometrium is sensitive to hormonal changes during the menstrual cycle. Estrogen thickens this lining, preparing for possible pregnancy. If pregnancy does not take place, progesterone levels reduce, leading to the shedding of the uterine lining, resulting in a menstrual period. How common is uterine cancer? Uterine cancer, especially endometrial cancer, is one of the most prevalent gynecological cancers worldwide. Its incidence is rising rapidly, with an estimated 50% increase in cases expected by 2040. What are the symptoms of uterine cancer? Symptoms of uterine cancer can be misleading, as they often resemble other conditions. Common symptoms include: Vaginal bleeding between periods or after menopause Lower abdominal pain or cramping Thin white or clear vaginal discharge in postmenopausal women Heavy or prolonged vaginal bleeding in women over 40 It's important to report any unusual symptoms to your healthcare provider for proper diagnosis and treatment. What causes uterine cancer? The exact cause of uterine cancer remains unknown. However, it is believed that changes in cells within the endometrium may lead to their uncontrolled growth and form a tumour. What are risk factors for uterine cancer? Various factors increase the risk of endometrial cancer: Age, Lifestyle, and Family History: Older age, obesity, or having a family history of conditions like Lynch Syndrome can increase the risk considerably Other Conditions: Conditions that increase estrogen levels without a proportionate increase in progesterone, such as obesity, diabetes, and polycystic ovary syndrome, can also elevate risk. Menstrual and Reproductive History: Women who started menstruating before age 12 or began menopause later have more exposure to estrogen which increases risk. Previous Treatments for Other Conditions: Taking hormone therapy may elevate the risk of endometrial cancer. These risk factors don’t guarantee the development of uterine cancer, but understanding them can help with early detection and management. What are the complications of endometrial cancer? Endometrial cancer, or uterine cancer, can result can potentially lead to life-threatening complications if it is not diagnosed early or managed effectively. Some complications may include: Anaemia: This condition is marked by a low number of red blood cells, which can occur if uterine cancer leads to heavy menstrual bleeding Uterine Perforation: This refers to a hole in the uterus that can occur during he process of dilation and curettage (D&C) or an endometrial biopsy, especially in women who are menopausal or have recently been pregnant Treatment Complications: Surgery, radiation, and chemotherapy can cause fatigue, changes in bowel and bladder function, lymphoedema, and vaginal vault prolapse Menopause: If you undergo ovary removal or certain treatments for endometrial cancer, it can induce sudden menopause Infertility: Surgery to remove the uterus or pelvic radiation can cause infertility Cancer Metastasis: This is when cancer cells spread from the uterus to other areas of the body Ineffective Treatment Response: Sometimes, your body may not respond well to treatment, leading to further complications How is uterine cancer diagnosed? If you observe any unusual symptoms or potential signs of uterine cancer, it’s crucial to consult your healthcare provider. After discussing your symptoms, risk factors, and family history, they may suggest various tests to help with diagnosis. Blood Tests: A CA-125 assay test measures the level of CA-125 protein in the blood which can be indicative of uterine cancer Imaging Tests: CT scans and MRI scans can reveal detailed images of your uterus to identify any abnormalities Transvaginal Ultrasound: A special probe is inserted into the vagina to capture the images of the uterus Endometrial Biopsy: A thin, flexible tube is passed through the cervix and into the uterus to remove a small amount of the endometrium for testing Hysteroscopy: A thin tube with light and a camera is inserted through the vagina and cervix to reach the uterus for detailed visualisation Dilation and Curettage (D&C): This procedure is undertaken in an operating room to remove uterine tissue for further testing What tests will we need to diagnose uterine cancer? The diagnostic process includes several tests like blood tests, imaging tests like CT and MRI scans, transvaginal ultrasound, endometrial biopsy, hysteroscopy, and dilation and curettage (D&C). The cells collected from are then analysed in a lab by a pathologist to confirm the presence of cancer. What else does an endometrial cancer diagnosis show? Once endometrial cancer is diagnosed, it's also crucial for your care team to determine its type, as this helps in developing the most effective treatment plan. There are two main types: Type 1 endometrial cancers are less aggressive and don't spread quickly Type 2 endometrial cancers exhibit more aggressive behaviour, often spreading beyond the uterus necessitating stronger treatment Additionally, determining the stage of cancer is important for prognosis: Stage I - Cancer hasn't spread beyond the uterus Stage II - Cancer has spread to the cervix Stage III - Cancer has spread to the vagina, ovaries or lymph nodes Stage IV - Cancer has metastasised beyond nearby organs How is uterine cancer treated? The treatment for uterine cancer varies based on the type of cancer and the patient's overall health. Common treatment options include: Surgery: A hysterectomy to remove the uterus is a common surgical procedure Chemotherapy: Powerful drugs are used to destroy cancer cells Radiation Therapy: High-energy radiation is targeted at cancer cells to destroy them Hormone Therapy: Hormones are used or blocked to treat cancer Immunotherapy: Enhances your immune system's ability to fight cancer Targeted Therapy: Medications target specific cancer cells, preventing them from multiplying What can I expect after uterine surgery? Uterine cancer surgery can cause side effects like: Infertility which means you can't get pregnant Menopause (if you were premenopausal and ovaries were removed), along with symptoms like vaginal dryness and night sweats Can uterine cancer be prevented? While it's impossible to completely prevent uterine cancer, certain lifestyle changes can help reduce your risk: Maintaining a Healthy Weight Being Physically Active Using Hormonal Contraceptives Managing Diabetes Seeking Treatment for Abnormal Bleeding Talking to Your Doctor Considering Your Family History Staying Up to Date on Screenings What’s the survival rate for people with uterine cancer? The survival rate for uterine cancer mainly depends on the stage at which it is diagnosed. The five-year survival rate is approximately 81%. However, if it is caught early and remains confined to the uterus, the survival rate can be as high as 95% Is there a cure for uterine cancer? While there is no guaranteed cure, uterine cancer treatment can be very effective if it is detected early and hasn't spread beyond the uterus. Surgical removal of the uterus may lead to a potential cure. Conclusion Understanding uterine cancer, its symptoms, causes, and treatment options, is crucial for early detection and effective management. While this information offers a complete overview, it's crucial to seek personalized medical advice from your healthcare provider. You should consider regular health checks for early detection and managing your health. Metropolis Healthcare offers at-home sample collection and advanced testing services, with quick online access to your test reports through email or the Metropolis TruHealth app. Remember, prioritising your health is an investment for a healthier tomorrow. So, take the first step towards empowering yourself with knowledge and proactive healthcare today!

Dealing with a bone cancer diagnosis can be challenging for you or your loved ones. You may have many questions about symptoms, causes, treatment options, and the stages of the disease. While this journey can be tough, understanding bone cancer can help make things easier. This blog aims to provide clear information on bone cancer, including the symptoms, causes, treatment, and stages, as well as survival rates. Our goal is to support you in managing your health. A bone cancer diagnosis can raise many questions for patients and their families. This article aims to help readers understand the condition better. This article will guide you through living with bone cancer, covering what it is, common symptoms like bone pain, possible causes, and available treatments. Knowing more about the condition can help patients feel more in control and at ease. What is Bone Cancer? Bone cancer is a serious condition characterized by abnormal cell growth in the bones. It can be classified as primary, which means it starts in the bone itself, or secondary, which occurs when cancer spreads to the bones from other areas of the body. However, primary bone cancers are less common than secondary ones. Among these primary bone cancers, the three most commonly diagnosed types such as Osteosarcoma, Ewing Sarcoma, and Chondrosarcoma. Osteosarcoma and Ewing Sarcoma primarily affect children and young adults, whereas Chondrosarcoma is more frequently seen in older individuals. Understanding these types is crucial for ensuring accurate diagnosis, effective treatment, and improved support for patients during their journey. How common is Bone Cancer? Bone cancer is relatively rare, making up approximately 1% of all cancer cases globally. However, it still represents to a considerable number of new diagnoses each year, with prevalence varying across different regions. Where does Bone Cancer usually start? Bone cancer can develop in any bone but most often affects the long bones, especially in the arms and legs like the femur, tibia, and humerus. A common symptoms include knee pain, which many patients describe as a dull ache that intensifies over time. This pain can become persistent, indicating the need for further evaluation. If someone is experiencing similar symptoms, it's important to consult a healthcare professional for an accurate and timely diagnosis along with appropriate care. In addition to knee pain, individuals may notice swelling or tenderness in the affected area. Other symptoms of bone cancer include limited range of motion, fatigue, unexplained weight loss, and a general sense of unwellness. As the cancer progresses bones weaken, resulting in fractures that happen more easily than expected, even due to minor falls or injuries. If you or someone you know is experiencing these symptoms, it's important to consult a healthcare professional for an evaluation. If someone is experiencing persistent knee pain or concerning symptoms, it is essential to seek medical attention. Early diagnosis and treatment are crucial for better outcomes in bone cancer. Doctors often use imaging tests, such as X-rays or MRIs, along with biopsies to confirm the presence of cancer. Early detection of these symptoms allows a prompt intervention, which is essential for effective treatment and management. Being aware of these symptoms enables individuals to take proactive steps regarding their health. Can a benign bone tumor become cancerous? Yes, benign (non-cancerous) bone tumors can sometimes become malignant (cancerous), but this is rare and usually not a major concern. It's important to keep an eye on benign tumors for any changes that might indicate they are turning cancerous. What should I know about Bone Cancer Staging? Bone cancer stages help determine the size of the tumor, where it is located, growth rate and whether it has spread to nearby lymph nodes or other parts of the body. The cancer stages are numbered from 1 (least severe) to 4 (most severe). Staging is based on factors like tumor size, location, growth rate, the number of bones involved, and if it has spread to other areas or lymph nodes. What are Bone Cancer Symptoms? The primary symptom of bone cancer is localised pain in the affected area. Other signs include swelling, unexpected fractures from minor injuries, or severe pain that continues even at rest. It’s crucial to remember that these symptoms aren’t unique to bone cancer and could be caused by other conditions. Common symptoms include pain, often in the knee, swelling of the bone, and fractures without major trauma. Because these symptoms can resemble those of other conditions, early detection is vital. What Causes Bone Cancer? The exact causes of bone cancer are unknown. However, certain genetic disorders and exposure to radiation may increase the risk. It's essential to highlight that many of the individuals diagnosed with bone cancer have no obvious risk factors. This uncertainty highlights why it's important to do more research to better understand what causes this disease. By learning more about bone cancer, we can improve prevention, diagnosis, and treatment options for those affected. How is Bone Cancer Diagnosed? Diagnosing bone cancer primarily involves using imaging tests like X-rays, MRI scans, PET scans, and CT scans. These images provide information about the location and size of the tumor. A definitive diagnosis is made through a biopsy, which involves extracting a tissue sample from the suspicious area for laboratory analysis. How is Bone Cancer Treated? Treatment for bone cancer varies based on its type and stage. A team of multidisciplinary specialists develops a tailored treatment plan for each patient. In cases of osteosarcoma, which is quite common, treatment typically starts with chemotherapy, followed by surgery and then additional chemotherapy. Contrary to common belief, modern treatments focus on limb salvage surgery whenever possible. Amputation is necessary only a small number of cases. Nearly 90% of cases undergo limb salvage surgery where the tumor is removed while preserving the limb's functionality. Can Bone Cancer Be Prevented? While there are no guaranteed preventive measures against bone cancer, maintaining overall health and wellness can help lower risk factors. Regular medical check-ups can also ensure early detection and timely intervention if any abnormalities surface. What is the Outlook for People with Bone Cancer? Many cases of bone cancer are effectively treated and managed. The success rate varies based on factors like the stage and type of cancer. For example, osteosarcoma has long-term survival rates of up to 70% if diagnosed before it spreads. This highlights importance of identifying the condition early and starting treatment right away. Is Bone Cancer Usually Fatal? The fatality rate of bone cancer depends on several factors, including the type of cancer, when it is diagnosed, and individual health. However, improvements in medical science have significantly increased survival rates over the years. How Long Can You Live with Bone Cancer? Again, life expectancy for individuals with bone cancer greatly depends on various factors. However, with early detection and appropriate treatment, many patients can live for many years following diagnosis. When to see a doctor? If you're experiencing persistent bone pain or have observed unusual changes in your bones like swelling or fractures without significant trauma, it's important to consult a healthcare provider immediately. What does Bone Cancer feel like? The main symptom of bone cancer is pain, but some tumors can be painless. The pain can range from mild or strong and is often described as throbbing, aching, or stabbing. Some people may also notice a lump in the affected area, which can be hard or soft to touch. Is there a connection between Osteoporosis and Bone Cancer? Although both conditions affect the bones, osteoporosis (which makes bones weak and brittle) does not directly lead to bone cancer. However, individual with osteoporosis are more prone to fractures, which can sometimes be confused with bone cancer symptoms because they may appear similar. Conclusion Living with bone cancer requires understanding your condition and making informed choices about your healthcare. Early detection and prompt intervention are key factors that can greatly improve survival rates. Understanding bone cancer symptoms, causes, treatment options, and stages enables you to make informed decisions about your health. While facing bone cancer can be difficult, it is not impossible to manage. Being knowledgeable about the condition can empower you to make informed decisions about your health. Be sure to consult your healthcare provider regularly for personalised advice. Additionally, consider using diagnostic services like those provided by Metropolis Healthcare for routine check-ups and early detection of any abnormalities. With their accurate pathology testing services conveniently available at home, prioritising your health becomes less daunting. Stay informed, stay healthy!