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Journals / Journal of Clinical and Experimental Investigations / 2014 / Cilt: 6 - Sayı: 1

Eritema nodozumun eşlik ettiği nadir idyopatik granülomatöz mastit olgusu

A rare case of idiopathic granulomatous mastitis associated with erythema nodosum

Hatice GÜMÜŞ
Edip Erdal YILMAZ
Ahmet TÜRKOĞLU
Ömer USLUKAYA
Metehan GÜMÜŞ
Pages
84–85
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

J Clin Exp Invest 2015; 6 (1): 84-85

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Idiopathic granulomatous mastitis (IGM) is a rare benign chronic inflammatory disease.
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Key Findings & Data:In this study, we presented 28-year-old female patient with IGM associated with erythema nodosum.
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Conclusion & Impact:J Clin Exp Invest 2015; 6 (1): 84-85
🔬Design:Research Article
📍Scope:2015 Verileri
⚙️Variables:Domain Parameters

Abstract

Idiopathic granulomatous mastitis (IGM) is a rare benign chronic inflammatory disease. Etiology is unknown, but an autoimmune mechanism is suspected. Erythema nodosum is rare extramammillary manifestation of IGM, and few cases have been reported in the literature. In this study, we presented 28-year-old female patient with IGM associated with erythema nodosum. IGM can be caused by autoimmune mechanism and treated with steroid or surgical treatment. J Clin Exp Invest 2015; 6 (1): 84-85

Özet

İdyopatik granulomatöz mastit (İGM) nadir kronik inflamatuar hastalıktır. Etyolojisi bilinmemektedir, fakat otoimmun mekanizmadan şüphelenilmektedir. Eritema nodozum İGM'nin nadir meme dışı bulgusudur ve literatürde az sayıda vaka bildirilmiştir. Bu çalışmada 28 yaşında eritema nodozumun eşlik ettiği İGM vakasını sunduk. İGM oto immun mekanizmayla oluşabilir ve steroid veya cerrahi yöntemle tedavi edilebilir

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Cite This Article

GÜMÜŞ, H., YILMAZ, E. E., TÜRKOĞLU, A., USLUKAYA, Ö., GÜMÜŞ, M. (2022). Eritema nodozumun eşlik ettiği nadir idyopatik granülomatöz mastit olgusu. Journal of Clinical and Experimental Investigations, Cilt: 6 - Sayı: 1, 84–85. https://ajindex.com/articles/561740

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References (7)

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