The May-Hegglin Anomaly in a Family
Journal of the Korean Pediatric Society
;
: 1449-1452, 1994.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Purpura
/
Granulocytes basophiles
/
Plaquettes
/
Monocytes
/
Épistaxis
/
Cytoplasme
/
Diagnostic
/
Granulocytes éosinophiles
/
Granulocytes neutrophiles
Type d'étude:
Etude diagnostique
Limites du sujet:
Enfant
/
Humains
/
Mâle
langue:
Coréen
Texte intégral:
Journal of the Korean Pediatric Society
Année:
1994
Type:
Article
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS