A Case of Sarcoidosis Disseminated to Skeletal Tissues

<span>Sarcoidosis is a systemic granulomatous disease of unknown etiology that typically affects young adults. Diagnostic criteria for sarcoidosis include involvement of two or more of the following organ systems: 1) pulmonary infiltrates; 2) bilateral hilar adenopathy; and 3) skin and/or eye...

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Main Authors: Edon Rabinowitz, Chinwe Ogedegbe, Joseph Feldman
Format: Article
Language:English
Published: University Library System, University of Pittsburgh 2013-11-01
Series:International Journal of Medical Students
Online Access:http://www.ijms.info/ojs/index.php/IJMS/article/view/11
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author Edon Rabinowitz
Chinwe Ogedegbe
Joseph Feldman
author_facet Edon Rabinowitz
Chinwe Ogedegbe
Joseph Feldman
author_sort Edon Rabinowitz
collection DOAJ
description <span>Sarcoidosis is a systemic granulomatous disease of unknown etiology that typically affects young adults. Diagnostic criteria for sarcoidosis include involvement of two or more of the following organ systems: 1) pulmonary infiltrates; 2) bilateral hilar adenopathy; and 3) skin and/or eye lesions. Musculoskeletal system is less commonly involved. For that reason potential presenting symptoms can vary and make the diagnosis very challenging; particularly if a patient has symptoms that mimic other conditions. Musculoskeletal involvement for example can mimic malignancy. The following case describes a patient with known history of primary metastatic mediastinal Germ Cell Tumor (GCT) with teratomatous elements who is diagnosed with sarcoidosis involving skeletal tissues.</span>
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spelling doaj.art-7ece98364b914b37b3e1e8ee821954c72023-09-03T09:37:41ZengUniversity Library System, University of PittsburghInternational Journal of Medical Students2076-63272013-11-0111434511A Case of Sarcoidosis Disseminated to Skeletal TissuesEdon RabinowitzChinwe OgedegbeJoseph Feldman<span>Sarcoidosis is a systemic granulomatous disease of unknown etiology that typically affects young adults. Diagnostic criteria for sarcoidosis include involvement of two or more of the following organ systems: 1) pulmonary infiltrates; 2) bilateral hilar adenopathy; and 3) skin and/or eye lesions. Musculoskeletal system is less commonly involved. For that reason potential presenting symptoms can vary and make the diagnosis very challenging; particularly if a patient has symptoms that mimic other conditions. Musculoskeletal involvement for example can mimic malignancy. The following case describes a patient with known history of primary metastatic mediastinal Germ Cell Tumor (GCT) with teratomatous elements who is diagnosed with sarcoidosis involving skeletal tissues.</span>http://www.ijms.info/ojs/index.php/IJMS/article/view/11
spellingShingle Edon Rabinowitz
Chinwe Ogedegbe
Joseph Feldman
A Case of Sarcoidosis Disseminated to Skeletal Tissues
International Journal of Medical Students
title A Case of Sarcoidosis Disseminated to Skeletal Tissues
title_full A Case of Sarcoidosis Disseminated to Skeletal Tissues
title_fullStr A Case of Sarcoidosis Disseminated to Skeletal Tissues
title_full_unstemmed A Case of Sarcoidosis Disseminated to Skeletal Tissues
title_short A Case of Sarcoidosis Disseminated to Skeletal Tissues
title_sort case of sarcoidosis disseminated to skeletal tissues
url http://www.ijms.info/ojs/index.php/IJMS/article/view/11
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