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Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report
BACKGROUND: Sarcoidosis is a multisystemic granulomatous disorder, which in nearly all cases involves the lungs and other organs. Isolated forms of sarcoidosis within the muscles, but without lung involvement, are extremely rare and can lead to delayed or even false diagnosis. CASE PRESENTATION: A 5...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569518/ https://www.ncbi.nlm.nih.gov/pubmed/28835264 http://dx.doi.org/10.1186/s13256-017-1403-3 |
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author | Meyer, Niklaus Sutter, Reto Schirp, Udo Gutzeit, Andreas |
author_facet | Meyer, Niklaus Sutter, Reto Schirp, Udo Gutzeit, Andreas |
author_sort | Meyer, Niklaus |
collection | PubMed |
description | BACKGROUND: Sarcoidosis is a multisystemic granulomatous disorder, which in nearly all cases involves the lungs and other organs. Isolated forms of sarcoidosis within the muscles, but without lung involvement, are extremely rare and can lead to delayed or even false diagnosis. CASE PRESENTATION: A 52-year-old white, Swiss man presented with painful arm cramps and a history of symptoms over the previous 3 years. In the initial clinical investigation, our patient also showed edema in both legs without any other complaints. After performing an magnetic resonance imaging scan of his extremities and a positron emission tomography/computed tomography scan, diffuse myositis was described. The subsequent muscle biopsy provided the surprising diagnosis of muscle sarcoidosis, without involvement of the lungs or any other organ. After starting therapy with glucocorticoids, his symptoms improved immediately. CONCLUSIONS: Sarcoidosis is a common disorder, which in most cases affects the lungs. In this case report an isolated sarcoidosis is described without lung involvement, but with involvement of the muscles of the extremities and the trunk. Reported cases of sarcoidosis only involving skeletal muscle and without lung involvement are extremely rare. Radiologists should consider this presentation of sarcoidosis to avoid delayed diagnosis and therapy. |
format | Online Article Text |
id | pubmed-5569518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55695182017-08-29 Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report Meyer, Niklaus Sutter, Reto Schirp, Udo Gutzeit, Andreas J Med Case Rep Case Report BACKGROUND: Sarcoidosis is a multisystemic granulomatous disorder, which in nearly all cases involves the lungs and other organs. Isolated forms of sarcoidosis within the muscles, but without lung involvement, are extremely rare and can lead to delayed or even false diagnosis. CASE PRESENTATION: A 52-year-old white, Swiss man presented with painful arm cramps and a history of symptoms over the previous 3 years. In the initial clinical investigation, our patient also showed edema in both legs without any other complaints. After performing an magnetic resonance imaging scan of his extremities and a positron emission tomography/computed tomography scan, diffuse myositis was described. The subsequent muscle biopsy provided the surprising diagnosis of muscle sarcoidosis, without involvement of the lungs or any other organ. After starting therapy with glucocorticoids, his symptoms improved immediately. CONCLUSIONS: Sarcoidosis is a common disorder, which in most cases affects the lungs. In this case report an isolated sarcoidosis is described without lung involvement, but with involvement of the muscles of the extremities and the trunk. Reported cases of sarcoidosis only involving skeletal muscle and without lung involvement are extremely rare. Radiologists should consider this presentation of sarcoidosis to avoid delayed diagnosis and therapy. BioMed Central 2017-08-24 /pmc/articles/PMC5569518/ /pubmed/28835264 http://dx.doi.org/10.1186/s13256-017-1403-3 Text en © The Author(s). 2017 Open AccessThis article is distributed 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 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 Meyer, Niklaus Sutter, Reto Schirp, Udo Gutzeit, Andreas Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
title | Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
title_full | Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
title_fullStr | Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
title_full_unstemmed | Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
title_short | Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
title_sort | extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569518/ https://www.ncbi.nlm.nih.gov/pubmed/28835264 http://dx.doi.org/10.1186/s13256-017-1403-3 |
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