Idiopathic Granulomatous Mastitis

Idiopathic granulomatous mastitis (IGM) is a rare, benign inflammatory disorder of the breast that is often underrecognized. The exact etiology and pathophysiology are unknown, but milk stasis is felt to play a role. Classically, this condition is noninfectious, but many cases are noted to be associ...

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Main Authors: Christina Dilaveri, Amy Degnim, Christine Lee, Daniel DeSimone, Dan Moldoveanu, Karthik Ghosh
Format: Article
Language:English
Published: Hindawi-Wiley 2024-01-01
Series:The Breast Journal
Online Access:http://dx.doi.org/10.1155/2024/6693720
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author Christina Dilaveri
Amy Degnim
Christine Lee
Daniel DeSimone
Dan Moldoveanu
Karthik Ghosh
author_facet Christina Dilaveri
Amy Degnim
Christine Lee
Daniel DeSimone
Dan Moldoveanu
Karthik Ghosh
author_sort Christina Dilaveri
collection DOAJ
description Idiopathic granulomatous mastitis (IGM) is a rare, benign inflammatory disorder of the breast that is often underrecognized. The exact etiology and pathophysiology are unknown, but milk stasis is felt to play a role. Classically, this condition is noninfectious, but many cases are noted to be associated with Corynebacterium species. Most patients affected are parous women with a mean age of 35, and many have breastfed within five years of diagnosis. Patients typically present with a painful mass and symptoms of inflammation, and these features can sometimes mimic breast cancer. Biopsy is needed to make a definitive diagnosis, and noncaseating granulomas are found on core biopsy. Many patients have a waxing and waning course over a period of six months to two years. Goal of treatment is to avoid surgery given poor wound healing, high risk of recurrence, and poor cosmetic outcomes. Medical treatment is preferred and includes observation, antibiotics, steroids, and immune modulators such as methotrexate. In more recent years, topical and intralesional steroids have become the treatment of choice, with similar outcomes to oral steroids.
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spelling doaj.art-cbda2ecb704a475d987ae8c92a20beb42024-02-02T00:00:01ZengHindawi-WileyThe Breast Journal1524-47412024-01-01202410.1155/2024/6693720Idiopathic Granulomatous MastitisChristina Dilaveri0Amy Degnim1Christine Lee2Daniel DeSimone3Dan Moldoveanu4Karthik Ghosh5Mayo ClinicMayo ClinicMayo ClinicMayo ClinicMayo ClinicMayo ClinicIdiopathic granulomatous mastitis (IGM) is a rare, benign inflammatory disorder of the breast that is often underrecognized. The exact etiology and pathophysiology are unknown, but milk stasis is felt to play a role. Classically, this condition is noninfectious, but many cases are noted to be associated with Corynebacterium species. Most patients affected are parous women with a mean age of 35, and many have breastfed within five years of diagnosis. Patients typically present with a painful mass and symptoms of inflammation, and these features can sometimes mimic breast cancer. Biopsy is needed to make a definitive diagnosis, and noncaseating granulomas are found on core biopsy. Many patients have a waxing and waning course over a period of six months to two years. Goal of treatment is to avoid surgery given poor wound healing, high risk of recurrence, and poor cosmetic outcomes. Medical treatment is preferred and includes observation, antibiotics, steroids, and immune modulators such as methotrexate. In more recent years, topical and intralesional steroids have become the treatment of choice, with similar outcomes to oral steroids.http://dx.doi.org/10.1155/2024/6693720
spellingShingle Christina Dilaveri
Amy Degnim
Christine Lee
Daniel DeSimone
Dan Moldoveanu
Karthik Ghosh
Idiopathic Granulomatous Mastitis
The Breast Journal
title Idiopathic Granulomatous Mastitis
title_full Idiopathic Granulomatous Mastitis
title_fullStr Idiopathic Granulomatous Mastitis
title_full_unstemmed Idiopathic Granulomatous Mastitis
title_short Idiopathic Granulomatous Mastitis
title_sort idiopathic granulomatous mastitis
url http://dx.doi.org/10.1155/2024/6693720
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AT karthikghosh idiopathicgranulomatousmastitis