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Clinical Findings and Therapy of Ureteral Duplication in 61 Children
Journal of the Korean Society of Pediatric Nephrology ; : 169-177, 1998.
Artigo em Coreano | WPRIM | ID: wpr-109708
ABSTRACT
Osteoclast-like giant cell tumor of the liver is an extremely rare malignancy with poor prognosis. To our knowledge, 5 cases have been reported in English literatures, but there was no report about fine needle aspiration cytologic(FNAC) features. We experienced a case of osteoclast-like giant cell tumor of the liver obtained by computed tomography(CT)-guided FNAC and needle biopsy. The cytologic findings mimicked giant cell tumor of the bone. A large hepatic mass of the left lobe with abdominal wall invasion was found by CT in a 46- year-old female complaining of epigastric pain. The FNAC showed moderately cellular smears consisting of osteoclast-like giant cells and mononuclear cells, which were individually scattered or intermingled in clusters. The osteoclast-like giant cells had abundant cytoplasms and multiple small round nuclei with fine chromatin and distinct nucleoli. The mononuclear cells had moderate amount of cytoplasm and relatively bland-looking oval nuclei with single small nucleoli. All of the cytologic features recapitulated the histologic findings of bland-looking osteoclast-like multinucleated giant cells evenly dispersed throughout the background of mononuclear cell. The immunohistochemical study showed positive reaction for CD68 and vimentin, but negative for cytokeratin in both osteoclast-like giant cells and mononuclear cells.
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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Biópsia Tipo de estudo: Estudo diagnóstico Limite: Criança / Feminino / Humanos / Masculino Idioma: Coreano Revista: Journal of the Korean Society of Pediatric Nephrology Ano de publicação: 1998 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Biópsia Tipo de estudo: Estudo diagnóstico Limite: Criança / Feminino / Humanos / Masculino Idioma: Coreano Revista: Journal of the Korean Society of Pediatric Nephrology Ano de publicação: 1998 Tipo de documento: Artigo