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Mammary sarcoidosis: A rare case report

INTRODUCTION: Sarcoidosis is an inflammatory, systemic, idiopathic disease characterized by multisystem involvement, of which mediastinal and pulmonary involvement is the most frequent. Mammary sarcoidosis is exceptional. CASE PRESENTATION: We report the case of a 50-year-old, diagnosed with mediast...

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Autores principales: Rhazari, Meriem, Ramdani, Abdelbassir, Gartini, Sara, Bouali, Siham, Aharmim, Mohammed, Thouil, Afaf, Kouismi, Hatim, Bourkadi, Jamal Eddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207054/
https://www.ncbi.nlm.nih.gov/pubmed/35734652
http://dx.doi.org/10.1016/j.amsu.2022.103892
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author Rhazari, Meriem
Ramdani, Abdelbassir
Gartini, Sara
Bouali, Siham
Aharmim, Mohammed
Thouil, Afaf
Kouismi, Hatim
Bourkadi, Jamal Eddine
author_facet Rhazari, Meriem
Ramdani, Abdelbassir
Gartini, Sara
Bouali, Siham
Aharmim, Mohammed
Thouil, Afaf
Kouismi, Hatim
Bourkadi, Jamal Eddine
author_sort Rhazari, Meriem
collection PubMed
description INTRODUCTION: Sarcoidosis is an inflammatory, systemic, idiopathic disease characterized by multisystem involvement, of which mediastinal and pulmonary involvement is the most frequent. Mammary sarcoidosis is exceptional. CASE PRESENTATION: We report the case of a 50-year-old, diagnosed with mediastinal and mammary sarcoidosis. Therapeutic abstention with clinical and radiological surveillance was recommended. The evolution was marked by a clear improvement (clinical and radiological). DISCUSSION: Mammary sarcoidosis is a rare anatomical and clinical entity which poses a problem of differential diagnosis with other granulomatous diseases and especially with breast carcinoma. The coexistence of systemic manifestations should lead to the discussion of sarcoidosis. CONCLUSION: Mammary sarcoidosis involvement is rare and is manifested by a mass with a smooth or spiculated border, requiring the exclusion of malignancy.
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spelling pubmed-92070542022-06-21 Mammary sarcoidosis: A rare case report Rhazari, Meriem Ramdani, Abdelbassir Gartini, Sara Bouali, Siham Aharmim, Mohammed Thouil, Afaf Kouismi, Hatim Bourkadi, Jamal Eddine Ann Med Surg (Lond) Case Report INTRODUCTION: Sarcoidosis is an inflammatory, systemic, idiopathic disease characterized by multisystem involvement, of which mediastinal and pulmonary involvement is the most frequent. Mammary sarcoidosis is exceptional. CASE PRESENTATION: We report the case of a 50-year-old, diagnosed with mediastinal and mammary sarcoidosis. Therapeutic abstention with clinical and radiological surveillance was recommended. The evolution was marked by a clear improvement (clinical and radiological). DISCUSSION: Mammary sarcoidosis is a rare anatomical and clinical entity which poses a problem of differential diagnosis with other granulomatous diseases and especially with breast carcinoma. The coexistence of systemic manifestations should lead to the discussion of sarcoidosis. CONCLUSION: Mammary sarcoidosis involvement is rare and is manifested by a mass with a smooth or spiculated border, requiring the exclusion of malignancy. Elsevier 2022-05-31 /pmc/articles/PMC9207054/ /pubmed/35734652 http://dx.doi.org/10.1016/j.amsu.2022.103892 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Rhazari, Meriem
Ramdani, Abdelbassir
Gartini, Sara
Bouali, Siham
Aharmim, Mohammed
Thouil, Afaf
Kouismi, Hatim
Bourkadi, Jamal Eddine
Mammary sarcoidosis: A rare case report
title Mammary sarcoidosis: A rare case report
title_full Mammary sarcoidosis: A rare case report
title_fullStr Mammary sarcoidosis: A rare case report
title_full_unstemmed Mammary sarcoidosis: A rare case report
title_short Mammary sarcoidosis: A rare case report
title_sort mammary sarcoidosis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207054/
https://www.ncbi.nlm.nih.gov/pubmed/35734652
http://dx.doi.org/10.1016/j.amsu.2022.103892
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