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Postpartum Polymyositis Following Intrauterine Fetal Death
Polymyositis (PM) is an uncommon inflammatory myopathy that affects striated muscles. It causes weakness of the limb girdles, neck, and pharyngeal muscles. We are presenting a case of PM which manifested after intrauterine death (IUD). The patient was referred to our hospital for breathing difficult...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Jaypee Brothers Medical Publishers
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519596/ https://www.ncbi.nlm.nih.gov/pubmed/33024387 http://dx.doi.org/10.5005/jp-journals-10071-23541 |
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author | Borse, Manmohan P Sahoo, Tapas K Anand, Kumar V Kumar, Manoj Panda, Debasish |
author_facet | Borse, Manmohan P Sahoo, Tapas K Anand, Kumar V Kumar, Manoj Panda, Debasish |
author_sort | Borse, Manmohan P |
collection | PubMed |
description | Polymyositis (PM) is an uncommon inflammatory myopathy that affects striated muscles. It causes weakness of the limb girdles, neck, and pharyngeal muscles. We are presenting a case of PM which manifested after intrauterine death (IUD). The patient was referred to our hospital for breathing difficulty, 4 days after delivery of a dead fetus. Initially, she was treated in line of puerperal sepsis and peripartum cardiomyopathy. Patient's cardiopulmonary functions improved but she had persistent high-grade fever. Gross muscle weakness was found on day 5 of admission, involving all four limbs, predominantly in proximal muscles and she had dark colored urine. Laboratory tests revealed myoglobinuria, high serum creatine phosphokinase (CPK) levels, and high lactate dehydrogenase (LDH) levels. Polymyositis diagnosed on the basis of high CPK levels, magnetic resonance imaging (MRI) of cervical spine, electromyography (EMG), and muscle biopsy findings. We question, whether the PM could be pathogenically related to the pregnancy? Literature review of the previously reported cases of PM/dermatomyositis and our case report suggests that pregnancy can trigger the new onset of PM. HOW TO CITE THIS ARTICLE: Borse MP, Sahoo TK, Anand KV, Kumar M, Panda D. Postpartum Polymyositis Following Intrauterine Fetal Death. Indian J Crit Care Med 2020;24(8):731–734. |
format | Online Article Text |
id | pubmed-7519596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-75195962020-10-05 Postpartum Polymyositis Following Intrauterine Fetal Death Borse, Manmohan P Sahoo, Tapas K Anand, Kumar V Kumar, Manoj Panda, Debasish Indian J Crit Care Med Case Report Polymyositis (PM) is an uncommon inflammatory myopathy that affects striated muscles. It causes weakness of the limb girdles, neck, and pharyngeal muscles. We are presenting a case of PM which manifested after intrauterine death (IUD). The patient was referred to our hospital for breathing difficulty, 4 days after delivery of a dead fetus. Initially, she was treated in line of puerperal sepsis and peripartum cardiomyopathy. Patient's cardiopulmonary functions improved but she had persistent high-grade fever. Gross muscle weakness was found on day 5 of admission, involving all four limbs, predominantly in proximal muscles and she had dark colored urine. Laboratory tests revealed myoglobinuria, high serum creatine phosphokinase (CPK) levels, and high lactate dehydrogenase (LDH) levels. Polymyositis diagnosed on the basis of high CPK levels, magnetic resonance imaging (MRI) of cervical spine, electromyography (EMG), and muscle biopsy findings. We question, whether the PM could be pathogenically related to the pregnancy? Literature review of the previously reported cases of PM/dermatomyositis and our case report suggests that pregnancy can trigger the new onset of PM. HOW TO CITE THIS ARTICLE: Borse MP, Sahoo TK, Anand KV, Kumar M, Panda D. Postpartum Polymyositis Following Intrauterine Fetal Death. Indian J Crit Care Med 2020;24(8):731–734. Jaypee Brothers Medical Publishers 2020-08 /pmc/articles/PMC7519596/ /pubmed/33024387 http://dx.doi.org/10.5005/jp-journals-10071-23541 Text en Copyright © 2020; Jaypee Brothers Medical Publishers (P) Ltd. © The Author(s). 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Borse, Manmohan P Sahoo, Tapas K Anand, Kumar V Kumar, Manoj Panda, Debasish Postpartum Polymyositis Following Intrauterine Fetal Death |
title | Postpartum Polymyositis Following Intrauterine Fetal Death |
title_full | Postpartum Polymyositis Following Intrauterine Fetal Death |
title_fullStr | Postpartum Polymyositis Following Intrauterine Fetal Death |
title_full_unstemmed | Postpartum Polymyositis Following Intrauterine Fetal Death |
title_short | Postpartum Polymyositis Following Intrauterine Fetal Death |
title_sort | postpartum polymyositis following intrauterine fetal death |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519596/ https://www.ncbi.nlm.nih.gov/pubmed/33024387 http://dx.doi.org/10.5005/jp-journals-10071-23541 |
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