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Chronic myelomonocytic leukaemia (an analysis of fourteen consecutive cases).
Article in English | IMSEAR | ID: sea-91787
ABSTRACT
Fourteen consecutive cases of chronic myelomonocytic leukaemia aged 6 to 73 (mean 40.5) years were reviewed to define the natural history of the disease and the risk of acute transformation. The common presenting features included anaemia, fever, purpura, and bleeding tendencies. Abnormal karyotypes were seen in 4 of 6 patients subjected to cytogenetic analysis. Low dose cytosine arabinoside achieved complete remission in two and partial remission in one, of the four patients treated with this modality. The mean survival was 5.6 (range 2-12) months and two patients) evolved to acute myeloid leukaemia. The long term survival with the present form of therapy in chronic myelomonocytic leukaemia is poor.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Biopsy, Needle / Blood Cell Count / Bone Marrow / Aged / Female / Humans / Male / Fetal Hemoglobin / Leukemia, Myelomonocytic, Chronic / Child Country/Region as subject: Asia Language: English Year: 1991 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Biopsy, Needle / Blood Cell Count / Bone Marrow / Aged / Female / Humans / Male / Fetal Hemoglobin / Leukemia, Myelomonocytic, Chronic / Child Country/Region as subject: Asia Language: English Year: 1991 Type: Article