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Lupus mastitis of the male breast

A 39-year-old male with no known co-morbid conditions presented with gradually increasing bilateral breast lumps for 1.5 years. Clinically, tender subcutaneous masses were detected. Mammograms revealed masses on both sides that on ultrasound were hyperechoic and showed internal vascularity. An MRI w...

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Detalles Bibliográficos
Autores principales: Thapa, Ajit, Parakh, Anushri, Arora, Jyoti, Goel, Ruchika Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180881/
https://www.ncbi.nlm.nih.gov/pubmed/30363642
http://dx.doi.org/10.1259/bjrcr.20150290
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author Thapa, Ajit
Parakh, Anushri
Arora, Jyoti
Goel, Ruchika Kumar
author_facet Thapa, Ajit
Parakh, Anushri
Arora, Jyoti
Goel, Ruchika Kumar
author_sort Thapa, Ajit
collection PubMed
description A 39-year-old male with no known co-morbid conditions presented with gradually increasing bilateral breast lumps for 1.5 years. Clinically, tender subcutaneous masses were detected. Mammograms revealed masses on both sides that on ultrasound were hyperechoic and showed internal vascularity. An MRI was suggested to assess the extent of the disease that confirmed bilateral masses but was otherwise inconclusive. Core biopsy revealed evidence of panniculitis with likely autoimmune aetiology. Evaluation of autoimmune markers was carried out that was positive and multidisciplinary team discussion concluded the diagnosis as lupus mastitis. Male breast pathology and lupus mastitis are both uncommon conditions, making lupus mastitis of male breast an extremely unusual presentation. However, its close clinical and radiological similarity with malignancy makes it important in spite of its rarity. Here we report a case of bilateral lupus mastitis in male breast with its radiological features.
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spelling pubmed-61808812018-10-25 Lupus mastitis of the male breast Thapa, Ajit Parakh, Anushri Arora, Jyoti Goel, Ruchika Kumar BJR Case Rep Case Report A 39-year-old male with no known co-morbid conditions presented with gradually increasing bilateral breast lumps for 1.5 years. Clinically, tender subcutaneous masses were detected. Mammograms revealed masses on both sides that on ultrasound were hyperechoic and showed internal vascularity. An MRI was suggested to assess the extent of the disease that confirmed bilateral masses but was otherwise inconclusive. Core biopsy revealed evidence of panniculitis with likely autoimmune aetiology. Evaluation of autoimmune markers was carried out that was positive and multidisciplinary team discussion concluded the diagnosis as lupus mastitis. Male breast pathology and lupus mastitis are both uncommon conditions, making lupus mastitis of male breast an extremely unusual presentation. However, its close clinical and radiological similarity with malignancy makes it important in spite of its rarity. Here we report a case of bilateral lupus mastitis in male breast with its radiological features. The British Institute of Radiology 2016-05-30 /pmc/articles/PMC6180881/ /pubmed/30363642 http://dx.doi.org/10.1259/bjrcr.20150290 Text en © 2015 The Authors. Published by the British Institute of Radiology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Thapa, Ajit
Parakh, Anushri
Arora, Jyoti
Goel, Ruchika Kumar
Lupus mastitis of the male breast
title Lupus mastitis of the male breast
title_full Lupus mastitis of the male breast
title_fullStr Lupus mastitis of the male breast
title_full_unstemmed Lupus mastitis of the male breast
title_short Lupus mastitis of the male breast
title_sort lupus mastitis of the male breast
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180881/
https://www.ncbi.nlm.nih.gov/pubmed/30363642
http://dx.doi.org/10.1259/bjrcr.20150290
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