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Published in: Archives of Gynecology and Obstetrics 4/2004

01-05-2004 | Review Article

Granulomatous mastitis

Authors: Dagmar Diesing, Roland Axt-Fliedner, Daniela Hornung, Jürgen M. Weiss, Klaus Diedrich, Michael Friedrich

Published in: Archives of Gynecology and Obstetrics | Issue 4/2004

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Abstract

Introduction

Granulomatous mastitis (GM) is a rare disease which predominantly occurs in premenopausal women shortly after their last childbirth.

Etiology

Its etiology is unclear, however, the disease has been shown to be correlated with breast-feeding and the use of oral contraceptives. An autoimmune component has also been discussed.

Presentation

It presents with the clinical symptoms of galactorrhea, inflammation, breast mass, tumorous indurations and ulcerations of the skin. In mammography and sonography nodular opacities and hypoechoic nodules are found. Very often clinical and radiological findings mimic breast cancer.

Histological diagnosis

The diagnosis is made by histopathology. Histological features in GM include signs of a chronic granulomatous inflammation with giant cells, leucocytes, epitheloid cells and macrophages as well as abscesses.

Treatment

Therapy of GM consists of complete surgical excision combined with oral steroid therapy, eventually in combination with anti-inflammatory drugs or colchicine. Use of methotrexate has also been successful. In case of formation of abscesses antibiotic therapy should be applied before steroid therapy. Immune-suppressive therapy should be performed until complete remission as rates of recurrence can be up to 50%.
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Metadata
Title
Granulomatous mastitis
Authors
Dagmar Diesing
Roland Axt-Fliedner
Daniela Hornung
Jürgen M. Weiss
Klaus Diedrich
Michael Friedrich
Publication date
01-05-2004
Publisher
Springer-Verlag
Published in
Archives of Gynecology and Obstetrics / Issue 4/2004
Print ISSN: 0932-0067
Electronic ISSN: 1432-0711
DOI
https://doi.org/10.1007/s00404-003-0561-2

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