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Myelodysplastic Syndrome with Delayed Maturation of Reticulocytes: A Report of Three Cases / 대한임상병리학회지
Article in Ko | WPRIM | ID: wpr-89889
Responsible library: WPRO
ABSTRACT
Anemia in myelodysplastic syndrome (MDS) is accompanied by reticulocytopenia in most patients. Reticulocytosis, when present, is generally less than appropriate to the degree of anemia and rarely exceeds 10%. In this report, three patients with MDS with persistent reticulocytosis are presented. In vitro reticulocyte survival studies have suggested that the reticulocytosis was caused by delay in maturation of the reticulocytes. Anemia with reticulocytosis, mimicking hemolytic disease, may be an unusual presentation of myelodysplastic syndrome, but, we emphasize that MDS should be included in the differential diagnosis of every patient presenting with anemia and high reticulocyte count. In vitro reticulotye survival study is easy to assess and valuable to diagnose this disease entity.
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Full text: 1 Index: WPRIM Main subject: Reticulocytes / Myelodysplastic Syndromes / Reticulocyte Count / Reticulocytosis / Diagnosis, Differential / Anemia Type of study: Diagnostic_studies Limits: Humans Language: Ko Journal: Korean Journal of Clinical Pathology Year: 1998 Type: Article
Full text: 1 Index: WPRIM Main subject: Reticulocytes / Myelodysplastic Syndromes / Reticulocyte Count / Reticulocytosis / Diagnosis, Differential / Anemia Type of study: Diagnostic_studies Limits: Humans Language: Ko Journal: Korean Journal of Clinical Pathology Year: 1998 Type: Article