Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2638
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dc.contributor.authorCetinkol, Yeliz-
dc.contributor.authorKorkmaz, Hakan-
dc.contributor.authorKorkmaz, Mukadder-
dc.contributor.authorUslu, Selen-
dc.date.accessioned2022-08-17T06:58:03Z-
dc.date.available2022-08-17T06:58:03Z-
dc.date.issued2016-
dc.identifier.urihttp://doi.org/10.2500/ar.2016.7.0152-
dc.identifier.urihttps://journals.sagepub.com/doi/10.2500/ar.2016.7.0152-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2638-
dc.description.abstractBackground: 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.en_US
dc.language.isoengen_US
dc.publisherOCEAN SIDE PUBLICATIONS INC, 95 PITMAN ST, PROVIDENCE, RI 02906 USAen_US
dc.relation.isversionof10.2500/ar.2016.7.0152en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDIAGNOSISen_US
dc.titleA rare presentation of sarcoidosis with nasal bone involvementen_US
dc.typearticleen_US
dc.relation.journalALLERGY & RHINOLOGYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-0988-4354en_US
dc.contributor.authorID0000-0003-4271-3140en_US
dc.contributor.authorID0000-0003-4940-4498en_US
dc.identifier.volume7en_US
dc.identifier.issue1en_US
dc.identifier.startpage45en_US
dc.identifier.endpage49en_US
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