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A rare presentation of sarcoidosis with nasal bone involvement
BACKGROUND: Sarcoidosis is a multisystem granulomatous inflammatory disease that is induced by infectious or noninfectious environmental antigens in a genetically susceptible host. Tuberculosis and sarcoidosis are two diseases with similar clinical and pathologic findings. The link between these two...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
OceanSide Publications, Inc.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837135/ https://www.ncbi.nlm.nih.gov/pubmed/27103561 http://dx.doi.org/10.2500/ar.2016.7.0152 |
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author | Korkmaz, Mukadder Uslu, Selen Korkmaz, Hakan Çetinkol, Yeliz |
author_facet | Korkmaz, Mukadder Uslu, Selen Korkmaz, Hakan Çetinkol, Yeliz |
author_sort | Korkmaz, Mukadder |
collection | PubMed |
description | BACKGROUND: Sarcoidosis is a multisystem granulomatous inflammatory disease that is induced by infectious or noninfectious environmental antigens in a genetically susceptible host. Tuberculosis and sarcoidosis are two diseases with similar clinical and pathologic findings. The link between these two diseases has been extensively studied. OBJECTIVE: Herein we describe a case of sarcoidosis associated with tuberculosis, treated for tuberculosis, and, 1 year, later presented with a nasal dorsal lump and skin lesions on the extremities. METHODS: Case report with clinical description. RESULTS: Our patient had a history of skin and cervical lymphadenopathy symptoms 1 year earlier and was treated with antituberculosis drugs in an outer medical center. Therapy had cured cervical lymphadenopathies, with no improvement in skin lesions. On appearance of the nasal dorsal lump, she presented to our outpatient clinic. We retrieved the previous specimens of the patient, which revealed coexistence of necrotizing granulomas with non-necrotizing granulomas, which was strongly indicative of the coexistence of tuberculosis and sarcoidosis. Radiologic, histopathologic, and microbiologic investigation revealed the diagnosis of sarcoidosis with nasal, cutaneous, and pulmonary involvement. Treatment with prednisolone and hydroxychloroquine resulted in dramatic improvement of nasal bone, pulmonary, and skin lesions within 2 weeks. CONCLUSION: The clinical presentation of sarcoidosis can be complex, and the differential diagnosis from tuberculosis can be challenging. Atypical clinical pictures also can cause delays in diagnosis and proper management. In patients with granulomatous lesions that are unresponsive to antituberculosis therapy, physicians must be alerted to the possibility of coexistent sarcoidosis. |
format | Online Article Text |
id | pubmed-4837135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | OceanSide Publications, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48371352016-04-27 A rare presentation of sarcoidosis with nasal bone involvement Korkmaz, Mukadder Uslu, Selen Korkmaz, Hakan Çetinkol, Yeliz Allergy Rhinol (Providence) Articles BACKGROUND: Sarcoidosis is a multisystem granulomatous inflammatory disease that is induced by infectious or noninfectious environmental antigens in a genetically susceptible host. Tuberculosis and sarcoidosis are two diseases with similar clinical and pathologic findings. The link between these two diseases has been extensively studied. OBJECTIVE: Herein we describe a case of sarcoidosis associated with tuberculosis, treated for tuberculosis, and, 1 year, later presented with a nasal dorsal lump and skin lesions on the extremities. METHODS: Case report with clinical description. RESULTS: Our patient had a history of skin and cervical lymphadenopathy symptoms 1 year earlier and was treated with antituberculosis drugs in an outer medical center. Therapy had cured cervical lymphadenopathies, with no improvement in skin lesions. On appearance of the nasal dorsal lump, she presented to our outpatient clinic. We retrieved the previous specimens of the patient, which revealed coexistence of necrotizing granulomas with non-necrotizing granulomas, which was strongly indicative of the coexistence of tuberculosis and sarcoidosis. Radiologic, histopathologic, and microbiologic investigation revealed the diagnosis of sarcoidosis with nasal, cutaneous, and pulmonary involvement. Treatment with prednisolone and hydroxychloroquine resulted in dramatic improvement of nasal bone, pulmonary, and skin lesions within 2 weeks. CONCLUSION: The clinical presentation of sarcoidosis can be complex, and the differential diagnosis from tuberculosis can be challenging. Atypical clinical pictures also can cause delays in diagnosis and proper management. In patients with granulomatous lesions that are unresponsive to antituberculosis therapy, physicians must be alerted to the possibility of coexistent sarcoidosis. OceanSide Publications, Inc. 2016 /pmc/articles/PMC4837135/ /pubmed/27103561 http://dx.doi.org/10.2500/ar.2016.7.0152 Text en Copyright © 2016, OceanSide Publications, Inc., U.S.A. This publication is provided under the terms of the Creative Commons Public License ("CCPL" or "License"), in attribution 3.0 unported (Attribution Non-Commercial No Derivatives (CC BY-NC-ND)), further described at: http://creativecommons.org/licenses/by-nc-nd/3.0/legalcode. The work is protected by copyright and/or other applicable law. Any use of the work other then as authorized under this license or copyright law is prohibited. |
spellingShingle | Articles Korkmaz, Mukadder Uslu, Selen Korkmaz, Hakan Çetinkol, Yeliz A rare presentation of sarcoidosis with nasal bone involvement |
title | A rare presentation of sarcoidosis with nasal bone involvement |
title_full | A rare presentation of sarcoidosis with nasal bone involvement |
title_fullStr | A rare presentation of sarcoidosis with nasal bone involvement |
title_full_unstemmed | A rare presentation of sarcoidosis with nasal bone involvement |
title_short | A rare presentation of sarcoidosis with nasal bone involvement |
title_sort | rare presentation of sarcoidosis with nasal bone involvement |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837135/ https://www.ncbi.nlm.nih.gov/pubmed/27103561 http://dx.doi.org/10.2500/ar.2016.7.0152 |
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