Chronic Granulocytic Leukemia in the Aged
- 1 November 1965
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of internal medicine (1960)
- Vol. 116 (5) , 765-775
- https://doi.org/10.1001/archinte.1965.03870050119018
Abstract
GHleukemia occurs at all ages ALTHOUGH leukemia occurs at all ages of life, chronic granulocytic leukemia (CGL) is predominantly a disease of young adult life and early middle age1-3(Fig 1). The usual case of CGL is that of a 20- to 50-year-old patient who complains of fatigue, a mass in the left subcostal region, or a sensation of fullness after eating. The spleen and liver are large and may half-fill the abdominal cavity. Laboratory studies usually reveal a leukocyte count that is greater than 100,000 cells/cu mm, with a predominance of granulocytes, including immature forms, and increased numbers of basophils. The cytoplasm of mature granulocytes contains a low concentration of alkaline phosphatase.4,5Serum vitamin B12levels are increased,6and recently a chromosomal abnormality was described which may precede the clinical onset of leukemia.7-9Treatment with radiation or chemotherapy usually produces improvement which lasts for months or years.10Then theThis publication has 8 references indexed in Scilit:
- Comparison of Philadelphia Chromosome-Positive and -Negative Patients with Chronic Myelocytic LeukemiaAnnals of Internal Medicine, 1964
- Chronic Granulocytic Leukemia and the Philadelphia ChromosomeBlood, 1963
- Chromosome Studies on Normal and Leukemic Human LeukocytesJNCI Journal of the National Cancer Institute, 1960
- Diseases or Clinical Conditions Associated with Low Leukocyte Alkaline PhosphataseNew England Journal of Medicine, 1960
- Hemorrhagic Thrombocythemia: A Critical ReviewBlood, 1960
- Serum Concentrations of Vitamin B12 in Patients Suffering from LeukemiaBlood, 1954
- ALKALINE PHOSPHATASE ACTIVITY IN NORMAL AND ABNORMAL HUMAN BLOOD AND BONE MARROW CELLS1946
- CHRONIC LEUKEMIAArchives of internal medicine (1960), 1939