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dc.contributor.authorOzsurekci, Yasemin
dc.contributor.authorCengiz, Ali B.
dc.contributor.authorDuzova, Ali
dc.contributor.authorSag, Erdal
dc.contributor.authorKadayifcilar, Sibel
dc.contributor.authorErsoz, Deniz Dogru
dc.contributor.authorAkcoren, Zuhal
dc.contributor.authorYuce, Aysel
dc.contributor.authorTavil, Betul
dc.contributor.authorAyvaz, Deniz
dc.contributor.authorAkyuz, Canan
dc.contributor.authorEroglu, Fehime Kara
dc.date.accessioned2019-12-10T10:50:04Z
dc.date.available2019-12-10T10:50:04Z
dc.date.issued2015
dc.identifier.issn0325-0075
dc.identifier.urihttps://doi.org/10.5546/aap.2015.eng.e336
dc.identifier.urihttp://hdl.handle.net/11655/14305
dc.description.abstractSarcoidosis, 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.
dc.language.isoen
dc.publisherSoc Argentina Pediatria
dc.relation.isversionof10.5546/aap.2015.eng.e336
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPediatrics
dc.titlePediatric-Onset Adult Type Sarcoidosis: A Case Report
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalArchivos Argentinos De Pediatria
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume113
dc.identifier.issue6
dc.identifier.startpageE336
dc.identifier.endpageE339
dc.description.indexWoS


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