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Acute Onset Polymyositis after Prolactinoma Extirpation
Hyperprolactinemia has been related to autoimmune diseases. Herein, we describe a case of a female with a prolactin producer pituitary macroadenoma who developed severe polymyositis one month after its removal. The patient had very high levels of CPK and muscle biopsy showed remarkable inflammatory...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241255/ https://www.ncbi.nlm.nih.gov/pubmed/25431724 http://dx.doi.org/10.1155/2014/329059 |
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author | Jakez-Ocampo, Juan Atisha-Fregoso, Yemil Llorente, Luis |
author_facet | Jakez-Ocampo, Juan Atisha-Fregoso, Yemil Llorente, Luis |
author_sort | Jakez-Ocampo, Juan |
collection | PubMed |
description | Hyperprolactinemia has been related to autoimmune diseases. Herein, we describe a case of a female with a prolactin producer pituitary macroadenoma who developed severe polymyositis one month after its removal. The patient had very high levels of CPK and muscle biopsy showed remarkable inflammatory infiltration. Steroid therapy was followed with total recovery. To the best of our knowledge, this is the first case reported of acute polymyositis after pituitary macroadenoma exeresis. |
format | Online Article Text |
id | pubmed-4241255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42412552014-11-27 Acute Onset Polymyositis after Prolactinoma Extirpation Jakez-Ocampo, Juan Atisha-Fregoso, Yemil Llorente, Luis Case Rep Rheumatol Case Report Hyperprolactinemia has been related to autoimmune diseases. Herein, we describe a case of a female with a prolactin producer pituitary macroadenoma who developed severe polymyositis one month after its removal. The patient had very high levels of CPK and muscle biopsy showed remarkable inflammatory infiltration. Steroid therapy was followed with total recovery. To the best of our knowledge, this is the first case reported of acute polymyositis after pituitary macroadenoma exeresis. Hindawi Publishing Corporation 2014 2014-11-06 /pmc/articles/PMC4241255/ /pubmed/25431724 http://dx.doi.org/10.1155/2014/329059 Text en Copyright © 2014 Juan Jakez-Ocampo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Jakez-Ocampo, Juan Atisha-Fregoso, Yemil Llorente, Luis Acute Onset Polymyositis after Prolactinoma Extirpation |
title | Acute Onset Polymyositis after Prolactinoma Extirpation |
title_full | Acute Onset Polymyositis after Prolactinoma Extirpation |
title_fullStr | Acute Onset Polymyositis after Prolactinoma Extirpation |
title_full_unstemmed | Acute Onset Polymyositis after Prolactinoma Extirpation |
title_short | Acute Onset Polymyositis after Prolactinoma Extirpation |
title_sort | acute onset polymyositis after prolactinoma extirpation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241255/ https://www.ncbi.nlm.nih.gov/pubmed/25431724 http://dx.doi.org/10.1155/2014/329059 |
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