Unsuspected Fanconi's Anemia and Bone Marrow Transplantation in Cases of Acute Myelomonocytic Leukemia
- 13 July 1989
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 321 (2) , 120-121
- https://doi.org/10.1056/nejm198907133210213
Abstract
To the Editor: Patients with Fanconi's anemia, a constitutional chromosomal-fragility syndrome in which hypoplastic anemia develops that is associated with diverse congenital abnormalities,1 have an abnormally high risk of malignant disease, especially acute myelomonocytic leukemia.2 The possibility of misdiagnosis in cases of Fanconi's anemia is considerable3; the hematologic features typical of the disorder may not develop in some cases until the third decade of life.4 Abnormally high levels of spontaneous chromosome breakage in cultured lymphocytes, bone marrow cells, or both are of great help in establishing the diagnosis.5 In very rare cases, acute myelomonocytic leukemia may be the first . . .Keywords
This publication has 7 references indexed in Scilit:
- Clinical and cytogenetic diversity in Fanconi's anaemia.Journal of Medical Genetics, 1984
- Radiosensitivity in Fanconi anaemia: application to the conditioning regimen for bone marrow transplantationBritish Journal of Haematology, 1983
- Fanconi's anemia treated by allogeneic marrow transplantationBlood, 1983
- Spectrum of anomalies in Fanconi anaemia.Journal of Medical Genetics, 1982
- Chromosome Abnormalities in Constitutional Aplastic AnemiaNew England Journal of Medicine, 1966
- Chronic Pancytopenia with Multiple Congenital Abnormalities (Fanconi's Anaemia)Acta Paediatrica, 1960
- FAMILIAL HYPOPLASTIC ANEMIA OF CHILDHOODAmerican Journal of Diseases of Children, 1947