Persistent Hypoplastic Acute Promyelocytic Leukemia with a Novel Chromosomal Abnormality of 46, XY, t(15;17), t(9;11)(q13;p13)
Author:
Affiliation:
1. Department ofHematology, Shinko Hospital
2. Department of Laboratory Medicine, Kobe City Medical Center General Hospital
Publisher
Japanese Society for Lymphoreticular Tissue Research
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jslrt/55/2/55_71/_pdf
Reference19 articles.
1. 1 Hillestad LK: Acute promyelocytic leukemia. Acta Med Scand 159:189-194, 1957
2. 2 Huang ME, Ye YC, Chen SR, Chai JR, Lu JX, et al.: Use of all-trans retinoic acid in the treatment of acute promyelocytic leukemia. Blood 72:567-572, 1988
3. 3 Ohno R, Asou N, Ohnishi K: Treatment of acute promyelocytic leukemia: strategy toward further increase of cure rate. Leukemia 17:1454-1463, 2003
4. 4 Rowley JD, Golomb HM, Dougherty C: 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia. Lancet 1:549-550, 1977
5. 5 de Thé H, Lavau C, Marchio A, Chomienne C, Degos L, et al.: The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR. Cell 66:675-684, 1991
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1. Hematopoietic status of the whole-body bone marrow in hypoplastic acute promyelocytic leukemia as evaluated by 18F-FLT PET/MRI;Annals of Hematology;2023-05-08
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