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Pediatric-onset adult type sarcoidosis: A case report
Author(s) -
Yasemin Ozsurekci,
Ali B Cengiz,
Ali Duzova,
Erdal Sag,
Sibel Kadayifcilar,
Deniz Dogru Ersoz,
Zuhal Akcoren,
Aysel Yuce,
Betul Tavil,
Deniz Ayvaz,
Canan Akyuz,
Fehime Kara Eroglu
Publication year - 2015
Publication title -
archivos argentinos de pediatría
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.236
H-Index - 19
eISSN - 1668-3501
pISSN - 0325-0075
DOI - 10.5546/aap.2015.eng.e336
Subject(s) - sarcoidosis , medicine , pediatrics , dermatology
Sarcoidosis, a multisystem disorder of unknown etiology that involves multiple organs, is rare in children. The true incidence and prevalence of childhood sarcoidosis is unknown. As in adults, many children with sarcoidosis may be asymptomatic; the disease may remain undiagnosed. A complete and systematic evaluation of the patient is essential for the sarcoidosis diagnosis in children. Here, we describe a case of 12-year-old female who presented with 2 years history of uveitis and hepatosplenomegaly. A chest computerized tomography revealed scattered peripheral pulmonary nodules and bilateral hiliar lymphadenopathy. Bone marrow aspiration and liver biopsy were not diagnostic. A lung biopsy showed non-necrotizing epithelioid cell granulomas. She was diagnosed with sarcoidosis according to demonstration of granulomatous inflammation and the exclusion of confusable entities

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