First report of granulomatous mastitis associated with Sjögren’s syndrome

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First report of granulomatous mastitis associated with Sjögren’s syndrome

Granulomatous mastitis is a rare and often considered as idiopathic disease. However, clinical examination and thorough diagnostic investigations have to be carried out in order to identify cases that are secondary to infections or systemic diseases since these forms may be cured with appropriate etiologic treatment. To the best of our knowledge, this report is the first to describe the associa...

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Idiopathic Granulomatous Mastitis Associated with Erythema Nodosum.

BACKGROUND Idiopathic granulomatous mastitis (IGM) is an uncommon benign chronic inflammatory breast disease, and erythema nodosum (EN) is an extremely rare systemic manifestation of IGM. Here, we report a rare case of IGM accompanied by EN. CASE REPORT A 32-year-old patient was admitted to our clinic with a history of a tender mass in the right breast. On physical examination, the right brea...

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Idiopathic Granulomatous Mastitis in Pregnancy: A Case Report

Idiopathic granulomatous mastitis is an inflammatory disease with unknown etiology. The clinical signs and mammograms of the disease can mimic breast cancer. The present study reports a case of idiopathic granulomatous mastitis in a pregnant woman. A 26-year-old woman, who was 24 weeks pregnant, felt a mass on her left breast. Biopsy of the mass revealed no evidence of malignancy. For treatment...

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surgical treatment of granulomatous mastitis associated with autoimmune response: report of a case

granulomatous mastitis (gm) is a rare breast disease with unknown etiology. clinical management strategies for gm include surgery, antibiotics, and steroid treatments. as patients with gm often respond to steroids, gm is thought to be an autoimmune disease. here we describe a case of trauma?induced gm that presented as autoimmune disease but was successfully treated by surgery without steroids....

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ژورنال

عنوان ژورنال: World Journal of Surgical Oncology

سال: 2013

ISSN: 1477-7819

DOI: 10.1186/1477-7819-11-268