İdiyopatik Granülomatöz Mastit
Özet
İdiyopatik granülomatöz mastit (IGM), sıklıkla mikroapselerin eşlik ettiği nonkazeifiye granülomlarla karakterize, meme kanserini taklit eden nadir ve benign inflamatuar bir meme hastalığıdır. Genellikle doğurganlık çağındaki ve yakın zamanda doğum/emzirme öyküsü olan kadınlarda görülür. Etiyolojisi tam olarak bilinmemekle birlikte hormonal dengesizlikler, otoimmünite, mikrobiyal ajanlar ve sigara kullanımı gibi faktörlerin rol oynadığı düşünülmektedir. En sık klinik bulgusu ağrılı, palpe edilebilen kitle ve eritamatöz cilt değişiklikleridir. Tanı aşamasında ultrasonografi, mamografi ve MRG gibi radyolojik yöntemlerden yararlanılsa da kesin tanı için altın standart, invaziv meme kanserini ekarte etmeyi sağlayan tru-cut biyopsisidir. Ayırıcı tanıda tüberküloz mastit ve duktus ektazisi gibi hastalıklar elenmelidir. IGM'nin optimal tedavisi hakkında fikir birliği olmasa da tedavi yaklaşımları arasında yakın takip, kortikosteroidler, immünosupresif ajanlar (metotreksat, azatiyoprin), sınırlı antibiyoterapi ve seçilmiş vakalarda komplet cerrahi eksizyon yer almaktadır. Hastalığın yönetiminde nüks riskini ve komplikasyonları azaltmak adına multidisipliner bir yaklaşım benimsenmelidir.
Idiopathic granulomatous mastitis (IGM) is a rare, benign inflammatory breast disease characterized by non-caseating granulomas often accompanied by microabscesses, mimicking breast carcinoma. It typically occurs in childbearing-aged women with a recent history of childbirth and breastfeeding. Although its etiology remains unknown, factors such as hormonal imbalances, autoimmunity, microbial agents, and smoking are thought to play a role. The most common clinical findings are a painful, palpable mass and erythematous skin changes. While radiological methods like ultrasonography, mammography, and MRI are utilized during the diagnosis phase, the gold standard for definitive diagnosis is tru-cut biopsy, which allows for the exclusion of invasive breast cancer. In differential diagnosis, conditions like tuberculous mastitis and duct ectasia must be ruled out. There is no consensus on the optimal treatment of IGM; however, therapeutic approaches include close observation, corticosteroids, immunosuppressive agents (methotrexate, azathioprine), limited antibiotic therapy, and complete surgical excision in selected cases. A multidisciplinary approach must be adopted in the management of the disease to reduce the risk of recurrence and complications.
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