Idiopathic granulomatous mastitis.


Journal

Cutis
ISSN: 2326-6929
Titre abrégé: Cutis
Pays: United States
ID NLM: 0006440

Informations de publication

Date de publication:
Jan 2019
Historique:
entrez: 14 2 2019
pubmed: 14 2 2019
medline: 7 6 2019
Statut: ppublish

Résumé

Idiopathic granulomatous mastitis (IGM) is a rare, poorly understood condition that presents as inflammatory nodules of the breast. It is often initially misdiagnosed as furunculosis or cellulitis. Despite the painful, scarring, and debilitating nature of the disease, patients often have a delay in accurate diagnosis and treatment. Even when IGM is considered as a diagnosis, it is one of exclusion, with the differential diagnosis including serious conditions such as breast cancer, sarcoidosis, and cutaneous tuberculosis. Therefore, appropriate workup is important. Given that IGM is a disease of the skin, it is important for dermatologists to be familiar with its presentation. We describe 3 cases of young women with this condition and demonstrate that identification of triggers or methotrexate treatment is highly successful in sparing patients the drastic surgical alternative of mastectomy.

Identifiants

pubmed: 30758334

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

38-42

Auteurs

Karyn Haitz (K)

Department of Dermatology and Cutaneous Surgery, University of Miami, Florida, USA.

Amy Ly (A)

Department of Pathology, Massachusetts General Hospital, Boston, USA.

Gideon Smith (G)

Department of Dermatology, Massachusetts General Hospital, Boston, USA.

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Classifications MeSH