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Pseudoreticulocytosis in a Case of Myelodysplastic Syndrome / 대한혈액학회지
Article in Korean | WPRIM (Western Pacific) | ID: wpr-720535
Responsible library: WPRO
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.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Reticulocytes / Bone Marrow / Myelodysplastic Syndromes / Reticulocyte Count / Reticulocytosis / Hematopoiesis / Anemia Limits: Humans Language: Korean Journal: Korean Journal of Hematology Year: 2001 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Reticulocytes / Bone Marrow / Myelodysplastic Syndromes / Reticulocyte Count / Reticulocytosis / Hematopoiesis / Anemia Limits: Humans Language: Korean Journal: Korean Journal of Hematology Year: 2001 Document type: Article
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