Preleukaemia
- 1 January 1968
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 39 (1), 20-28
- https://doi.org/10.1159/000208937
Abstract
Four cases of preleukemia were studied from onset to death. They presented with a deficiency of at least 1 of the cellular components of the peripheral blood, a hyperplastic marrow and no enlargement of spleen or lymph nodes. Extensive investigations were not diagnostic until a terminal stage was reached. The nature of preleukemia is discussed and it is suggested that it is the manifestation of a slow growing, occult, leukemic process rather than a definitive hemato-logical condition with a sporadic proclivity to leukemic transformation.This publication has 10 references indexed in Scilit:
- Chromosome Studies in PreleukemiaBlood, 1966
- Sideroblastic Anaemia: Is This a Malignancy?British Journal of Haematology, 1965
- THE ACUTE LEUKAEMIAS: A STUDY OF 580 PATIENTS1QJM: An International Journal of Medicine, 1964
- Acquired Pseudo-Pelger Anomaly of Granulocytic LeukocytesNew England Journal of Medicine, 1959
- APLASTIC ANEMIA: AN ANALYSIS OF 50 CASESAnnals of Internal Medicine, 1958
- Acute Leukemia Over the Age of Fifty: A Study of Its Incidence and Natural HistoryBlood, 1956
- Chronic Refractory Anemia with Sideroblastic Bone Marrow: A Study of Four CasesBlood, 1956
- Myeloblastic Leukemia Preceded by Prolonged Hematologic DisorderBlood, 1955
- EARLY ATYPICAL MANIFESTATIONS OF LEUKEMIAAnnals of Internal Medicine, 1954
- Pelger-like Leucocytes in Chronic Myeloid LeukaemiaActa Haematologica, 1954