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Rare Presentations of Sarcoidosis: A Case Series
Sarcoidosis is a systemic disease of unknown etiology with multi-system affection. It typically involves the skin, eyes, hilar lymph nodes, and pulmonary parenchyma. However, as any organ system could be involved, one has to be aware of its atypical manifestations. We present three uncommon manifest...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163919/ https://www.ncbi.nlm.nih.gov/pubmed/37159764 http://dx.doi.org/10.7759/cureus.37208 |
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author | Kamath, Sangita D Upadhyay, Ajatshatru Jakka, Sreedevi |
author_facet | Kamath, Sangita D Upadhyay, Ajatshatru Jakka, Sreedevi |
author_sort | Kamath, Sangita D |
collection | PubMed |
description | Sarcoidosis is a systemic disease of unknown etiology with multi-system affection. It typically involves the skin, eyes, hilar lymph nodes, and pulmonary parenchyma. However, as any organ system could be involved, one has to be aware of its atypical manifestations. We present three uncommon manifestations of the disease. Our first case presented with fever, arthralgias, and right hilar lymphadenopathy with a history of tuberculosis in the past. He was treated for tuberculosis but had a relapse of symptoms three months after completion of treatment. The second patient presented with a headache for two months. On evaluation, cerebrospinal fluid examination showed evidence of aseptic meningitis, while an MRI of the brain demonstrated enhancement of the basal meninges. The third patient was admitted with a mass on the left side of the neck for one year. On evaluation, he was found to have left cervical lymphadenopathy, with its biopsy showing non-caseating epitheloid granuloma. Immunofluorescence did not show evidence of leukemia or lymphoma. All the patients had negative tuberculin skin tests and elevated serum angiotensin-converting enzyme levels supporting the diagnosis of sarcoidosis. They were treated with steroids with complete resolution of symptoms and no recurrence at follow-up. Sarcoidosis is an underdiagnosed entity in India. Thus, awareness of the atypical clinical features could lead to early recognition of the disease and its treatment. |
format | Online Article Text |
id | pubmed-10163919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-101639192023-05-07 Rare Presentations of Sarcoidosis: A Case Series Kamath, Sangita D Upadhyay, Ajatshatru Jakka, Sreedevi Cureus Internal Medicine Sarcoidosis is a systemic disease of unknown etiology with multi-system affection. It typically involves the skin, eyes, hilar lymph nodes, and pulmonary parenchyma. However, as any organ system could be involved, one has to be aware of its atypical manifestations. We present three uncommon manifestations of the disease. Our first case presented with fever, arthralgias, and right hilar lymphadenopathy with a history of tuberculosis in the past. He was treated for tuberculosis but had a relapse of symptoms three months after completion of treatment. The second patient presented with a headache for two months. On evaluation, cerebrospinal fluid examination showed evidence of aseptic meningitis, while an MRI of the brain demonstrated enhancement of the basal meninges. The third patient was admitted with a mass on the left side of the neck for one year. On evaluation, he was found to have left cervical lymphadenopathy, with its biopsy showing non-caseating epitheloid granuloma. Immunofluorescence did not show evidence of leukemia or lymphoma. All the patients had negative tuberculin skin tests and elevated serum angiotensin-converting enzyme levels supporting the diagnosis of sarcoidosis. They were treated with steroids with complete resolution of symptoms and no recurrence at follow-up. Sarcoidosis is an underdiagnosed entity in India. Thus, awareness of the atypical clinical features could lead to early recognition of the disease and its treatment. Cureus 2023-04-06 /pmc/articles/PMC10163919/ /pubmed/37159764 http://dx.doi.org/10.7759/cureus.37208 Text en Copyright © 2023, Kamath et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Internal Medicine Kamath, Sangita D Upadhyay, Ajatshatru Jakka, Sreedevi Rare Presentations of Sarcoidosis: A Case Series |
title | Rare Presentations of Sarcoidosis: A Case Series |
title_full | Rare Presentations of Sarcoidosis: A Case Series |
title_fullStr | Rare Presentations of Sarcoidosis: A Case Series |
title_full_unstemmed | Rare Presentations of Sarcoidosis: A Case Series |
title_short | Rare Presentations of Sarcoidosis: A Case Series |
title_sort | rare presentations of sarcoidosis: a case series |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163919/ https://www.ncbi.nlm.nih.gov/pubmed/37159764 http://dx.doi.org/10.7759/cureus.37208 |
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