The May-Hegglin Anomaly in a Family
Journal of the Korean Pediatric Society
;
: 1449-1452, 1994.
Artigo
em Coreano
| WPRIM
| ID: wpr-84939
ABSTRACT
The May-Hegglin anomaly is a rare autosomal dominant trait characterized by platelet abnormalities in the peripheral blood and large (up to 5mu) pale blue staining inclusions in the cytoplasm of neutrophils, eosinophils, basophils, and monocytes. We experienced a case of May-Hegglin anomaly in a 7 year old male and another case out of his family. His initial complaints at the admission were petechiae and intermittent epistaxis. Diagnosis was confirmed by peripheral blood smear and family study. We report the case with brief review of related literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Púrpura
/
Basófilos
/
Plaquetas
/
Monócitos
/
Epistaxe
/
Citoplasma
/
Diagnóstico
/
Eosinófilos
/
Neutrófilos
Tipo de estudo:
Estudo diagnóstico
Limite:
Criança
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Pediatric Society
Ano de publicação:
1994
Tipo de documento:
Artigo
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