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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.
Artículo en 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.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fragilidad Osmótica / Esferocitosis Hereditaria / Prueba de Coombs / Eosina Amarillenta-(YS) / Diagnóstico Diferencial / Eritrocitos / Citometría de Flujo / Anemia Hemolítica Tipo de estudio: Estudio diagnóstico Límite: Niño / Humanos / Masculino Idioma: Coreano Revista: The Korean Journal of Laboratory Medicine Año: 2010 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fragilidad Osmótica / Esferocitosis Hereditaria / Prueba de Coombs / Eosina Amarillenta-(YS) / Diagnóstico Diferencial / Eritrocitos / Citometría de Flujo / Anemia Hemolítica Tipo de estudio: Estudio diagnóstico Límite: Niño / Humanos / Masculino Idioma: Coreano Revista: The Korean Journal of Laboratory Medicine Año: 2010 Tipo del documento: Artículo