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Flow-Assisted Differential Diagnosis of Hemolytic Anemia with Spherocytosis: A Case Report / 대한진단검사의학회지
The Korean Journal of Laboratory Medicine ; : 339-344, 2010.
Artigo em Coreano | WPRIM | ID: wpr-77844
ABSTRACT
In patients with hemolytic anemia associated with spherocytosis, differential diagnosis has to be made whether the hemolysis is immune-mediated or of non-immune origin. We report a case of hereditary spherocytosis in a 12-yr-old male child, in whom flow-assisted diagnosis was made. In this case, diagnosis was not determined because routine laboratory workups for hereditary spherocytosis yielded discrepant

RESULTS:

positive osmotic fragility test, positive direct antiglobulin test, and normal result in the red cell membrane protein sodium dodecyl succinimide polyacrylamide gel electrophoresis. However, all flow cytometry-based tests, such as osmotic fragility, direct antiglobulin, and eosin 5-maleimide binding test, yielded results compatible with hereditary spherocytosis. Additionally, in family study, the results of eosin 5-maleimide binding test suggested his disease being hereditary. In cases with diagnostic difficulties, flow cytometry may be used as an alternative tool, which can provide additional information in the differential diagnosis of hemolytic anemia with spherocytosis.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fragilidade Osmótica / Esferocitose Hereditária / Teste de Coombs / Amarelo de Eosina-(YS) / Diagnóstico Diferencial / Eritrócitos / Citometria de Fluxo / Anemia Hemolítica Tipo de estudo: Estudo diagnóstico Limite: Criança / Humanos / Masculino Idioma: Coreano Revista: The Korean Journal of Laboratory Medicine Ano de publicação: 2010 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fragilidade Osmótica / Esferocitose Hereditária / Teste de Coombs / Amarelo de Eosina-(YS) / Diagnóstico Diferencial / Eritrócitos / Citometria de Fluxo / Anemia Hemolítica Tipo de estudo: Estudo diagnóstico Limite: Criança / Humanos / Masculino Idioma: Coreano Revista: The Korean Journal of Laboratory Medicine Ano de publicação: 2010 Tipo de documento: Artigo