Pseudoreticulocytosis in a Case of Myelodysplastic Syndrome / 대한혈액학회지
Korean Journal of Hematology
;
: 176-179, 2001.
Artículo
en Coreano
| WPRIM
| ID: wpr-720535
ABSTRACT
Myelodysplastic syndrome (MDS) is a group of hematopoietic disorders characterized by ineffective hematopoiesis and peripheral cytopenia associated with dysplastic hypercellular marrow. Anemia is a frequent finding and reticulocytes are usually normal or slightly decreased in the patients with MDS. "Pseudoreticulocytosis" is a rare abnormality of patients with MDS. In these patients, the delayed maturation of reticulocytes is revealed and unusual reticulocytosis occurs with the decreased red cell production. We report a case of MDS characterized by the anemia associated with high reticulocyte count. 'In vitro reticulocyte survival test' showed that the reticulocytosis was a consequence of delayed maturation.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Reticulocitos
/
Médula Ósea
/
Síndromes Mielodisplásicos
/
Recuento de Reticulocitos
/
Reticulocitosis
/
Hematopoyesis
/
Anemia
Límite:
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Hematology
Año:
2001
Tipo del documento:
Artículo
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