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Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review
Sarcoidosis is a systemic granulomatous disease of the lungs that commonly involves intrathoracic lymph nodes. Here, we report the case of a 68-year-old woman who complained of shortness of breath and had suffered from the enlargement of intrathoracic lymph nodes for 12 years, swelling of the right...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528272/ https://www.ncbi.nlm.nih.gov/pubmed/37761357 http://dx.doi.org/10.3390/diagnostics13182990 |
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author | Feng, Haoshen Ma, Jiangwei Zhao, Yabin Zheng, Rui Wang, Wei |
author_facet | Feng, Haoshen Ma, Jiangwei Zhao, Yabin Zheng, Rui Wang, Wei |
author_sort | Feng, Haoshen |
collection | PubMed |
description | Sarcoidosis is a systemic granulomatous disease of the lungs that commonly involves intrathoracic lymph nodes. Here, we report the case of a 68-year-old woman who complained of shortness of breath and had suffered from the enlargement of intrathoracic lymph nodes for 12 years, swelling of the right middle finger for 7 years, and nasal obstruction for 2 years. The damage to the phalange was aggravated continuously and a malignant lesion could not be excluded, thus leading to amputation of the right middle finger. Pathological data indicated chronic inflammatory granulomatous disease and anti-acid staining was negative. Examination of the paranasal sinuses indicated destruction of the sinonasal bone and the swollen mucosa. Combined with the elevated ratio of CD4+/CD8+ T cells in bronchoalveolar lavage fluid and other results, the patient was finally diagnosed with sarcoidosis and received corticosteroid therapy. The shortness of breath and abnormality of the nose were significantly improved after treatment. Our case demonstrated the process of differential diagnosis for systemic granulomatous diseases, indicating the necessity of corticosteroid therapy for systematic sarcoidosis. |
format | Online Article Text |
id | pubmed-10528272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105282722023-09-28 Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review Feng, Haoshen Ma, Jiangwei Zhao, Yabin Zheng, Rui Wang, Wei Diagnostics (Basel) Case Report Sarcoidosis is a systemic granulomatous disease of the lungs that commonly involves intrathoracic lymph nodes. Here, we report the case of a 68-year-old woman who complained of shortness of breath and had suffered from the enlargement of intrathoracic lymph nodes for 12 years, swelling of the right middle finger for 7 years, and nasal obstruction for 2 years. The damage to the phalange was aggravated continuously and a malignant lesion could not be excluded, thus leading to amputation of the right middle finger. Pathological data indicated chronic inflammatory granulomatous disease and anti-acid staining was negative. Examination of the paranasal sinuses indicated destruction of the sinonasal bone and the swollen mucosa. Combined with the elevated ratio of CD4+/CD8+ T cells in bronchoalveolar lavage fluid and other results, the patient was finally diagnosed with sarcoidosis and received corticosteroid therapy. The shortness of breath and abnormality of the nose were significantly improved after treatment. Our case demonstrated the process of differential diagnosis for systemic granulomatous diseases, indicating the necessity of corticosteroid therapy for systematic sarcoidosis. MDPI 2023-09-18 /pmc/articles/PMC10528272/ /pubmed/37761357 http://dx.doi.org/10.3390/diagnostics13182990 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Feng, Haoshen Ma, Jiangwei Zhao, Yabin Zheng, Rui Wang, Wei Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review |
title | Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review |
title_full | Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review |
title_fullStr | Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review |
title_full_unstemmed | Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review |
title_short | Sarcoidosis with Severe Bone Involvement: A Case Report and Literature Review |
title_sort | sarcoidosis with severe bone involvement: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528272/ https://www.ncbi.nlm.nih.gov/pubmed/37761357 http://dx.doi.org/10.3390/diagnostics13182990 |
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