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Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review
This study was performed to describe a rare case of granulomatous lobular mastitis (GLM) that was successfully treated with bromocriptine in a male patient with gynecomastia and hyperprolactinemia. A 20-year-old man presented with a 1-year history of breast enlargement and galactorrhea. Physical exa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811439/ https://www.ncbi.nlm.nih.gov/pubmed/35098766 http://dx.doi.org/10.1177/03000605221075815 |
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author | Yin, Liang Agyekum, Enock Adjei Zhang, Qing Wu, Ting Qian, Xiaoqin |
author_facet | Yin, Liang Agyekum, Enock Adjei Zhang, Qing Wu, Ting Qian, Xiaoqin |
author_sort | Yin, Liang |
collection | PubMed |
description | This study was performed to describe a rare case of granulomatous lobular mastitis (GLM) that was successfully treated with bromocriptine in a male patient with gynecomastia and hyperprolactinemia. A 20-year-old man presented with a 1-year history of breast enlargement and galactorrhea. Physical examination revealed bilateral breast enlargement, porous discharge, and a 3-cm left breast lump in the 10-o’clock quadrant. Magnetic resonance imaging of the brain showed a 1.2-mm pituitary tumor. Laboratory analysis revealed hyperprolactinemia with low serum testosterone and elevated prolactin and estradiol levels. The lump in the left breast was examined by ultrasonography and mammography, and a core needle biopsy revealed chronic inflammation. The patient’s galactorrhea and breast lump disappeared after 3 months of treatment with bromocriptine at 2.5 mg once a day. His serum prolactin level also normalized. Following a review of this case, the patient was diagnosed with gynecomastia with hyperprolactinemia complicated by rare GLM. To the best of our knowledge, this is the first reported case of concurrent gynecomastia and GLM. |
format | Online Article Text |
id | pubmed-8811439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-88114392022-02-04 Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review Yin, Liang Agyekum, Enock Adjei Zhang, Qing Wu, Ting Qian, Xiaoqin J Int Med Res Case Reports This study was performed to describe a rare case of granulomatous lobular mastitis (GLM) that was successfully treated with bromocriptine in a male patient with gynecomastia and hyperprolactinemia. A 20-year-old man presented with a 1-year history of breast enlargement and galactorrhea. Physical examination revealed bilateral breast enlargement, porous discharge, and a 3-cm left breast lump in the 10-o’clock quadrant. Magnetic resonance imaging of the brain showed a 1.2-mm pituitary tumor. Laboratory analysis revealed hyperprolactinemia with low serum testosterone and elevated prolactin and estradiol levels. The lump in the left breast was examined by ultrasonography and mammography, and a core needle biopsy revealed chronic inflammation. The patient’s galactorrhea and breast lump disappeared after 3 months of treatment with bromocriptine at 2.5 mg once a day. His serum prolactin level also normalized. Following a review of this case, the patient was diagnosed with gynecomastia with hyperprolactinemia complicated by rare GLM. To the best of our knowledge, this is the first reported case of concurrent gynecomastia and GLM. SAGE Publications 2022-01-30 /pmc/articles/PMC8811439/ /pubmed/35098766 http://dx.doi.org/10.1177/03000605221075815 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Yin, Liang Agyekum, Enock Adjei Zhang, Qing Wu, Ting Qian, Xiaoqin Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
title | Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
title_full | Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
title_fullStr | Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
title_full_unstemmed | Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
title_short | Gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
title_sort | gynecomastia with rare granulomatous lobular mastitis: a case report and literature review |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811439/ https://www.ncbi.nlm.nih.gov/pubmed/35098766 http://dx.doi.org/10.1177/03000605221075815 |
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