Prolonged Extreme Thrombocytosis in a Postsplenectomy Patient with Hereditary Spherocytosis
Korean Journal of Hematology
;
: 298-303, 2009.
Article
Dans Anglais
| WPRIM
| ID: wpr-720068
ABSTRACT
We report a case of prolonged extreme reactive thrombocytosis in a post-splenectomy patient with hereditary spherocytosis. A 29-year-old female patient presented with gall stones detected incidentally by abdominal ultrasonography. Her laboratory findings showed hemolytic anemia with spherocytosis on the peripheral blood smear and increased osmotic fragility. She was diagnosed with hereditary spherocytosis and underwent a laparoscopic cholecystectomy and splenectomy. After undergoing surgery, the hemolytic anemia was resolved but thrombocytosis was newly detected. Nineteen months after the splenectomy, the thrombocytosis was still persistent and extremely high. To our knowledge, this is the first report of a prolonged extreme reactive thrombocytosis after a splenectomy in Korea.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Fragilité osmotique
/
Sphérocytose héréditaire
/
Splénectomie
/
Thrombocytose
/
Calculs biliaires
/
Cholécystectomie laparoscopique
/
Anémie hémolytique
/
Corée
Limites du sujet:
Adulte
/
Femelle
/
Humains
Pays comme sujet:
Asie
langue:
Anglais
Texte intégral:
Korean Journal of Hematology
Année:
2009
Type:
Article
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