Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2638
Title: A rare presentation of sarcoidosis with nasal bone involvement
Authors: Cetinkol, Yeliz
Korkmaz, Hakan
Korkmaz, Mukadder
Uslu, Selen
Ordu Üniversitesi
0000-0002-0988-4354
0000-0003-4271-3140
0000-0003-4940-4498
Keywords: DIAGNOSIS
Issue Date: 2016
Publisher: OCEAN SIDE PUBLICATIONS INC, 95 PITMAN ST, PROVIDENCE, RI 02906 USA
Abstract: 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.
URI: http://doi.org/10.2500/ar.2016.7.0152
https://journals.sagepub.com/doi/10.2500/ar.2016.7.0152
http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2638
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