To the Editor: Translocation t(9;22)(q34;q11) is found in 1-2% of newly diagnosed patients with de novo AML. The prognosis of Ph ΓΎ AML is very poor with a median survival time of only 7 months. We present two patients with de novo Ph ΓΎ AML who received induction chemotherapy and post-remission imati
Morphologic and cytochemical characteristics of acute promyelocytic leukemia
β Scribed by F. R. Davey; R. B. Davis; J. M. Maccallum; D. A. Nelson; R. J. Mayer; E. D. Ball; J. D. Griffin; C. A. Schiffer; C. D. Bloomfield
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 1017 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
β¦ Synopsis
The existence of two distinct subtypes of acute promyelocytic leukemia was confirmed and characterized based on morphologic features of leukemic cells in a series of 63 patients studied by the Cancer and Leukemia Group B (CALGB). Seventeen patients (27%) had microgranular leukemic cells (M3V), and 46 patients (73%) had hypergranular leukemic cells (M3). These patient cohorts were studied for other laboratory and clinical features. Leukemic cells from M3V patients stained less frequently than leukemic cells from M3 patients for myeloperoxidase (median, 93% vs. 99%; P=.006), periodic acid-Schiff (median, 57% vs. 92%; P= .OOOl), ASD-chloroacetate esterase (median, 45% vs. 87%; P<.OOOl), and alpha-naphthyl acetate esterase (0% vs. 37%; P= .003). Patients with M3V had a higher platelet count (median, 50 vs. 30 x 10g/L; P=.O1) and tended to have a higher leukocyte count (median, 7.4 vs. 2.2 x 10g/L; P=.06) than M3 patients. The patients with Y3V morphology were more likely to be nonwhite (29% vs. 7%; P=.O3), female (71% vs. 37%; P= .02), and to be infected at the time of presentation (71% vs. 35%; P= .02). No differences in the frequency of the t(15;17) karyotype or the immunophenotypic expression of the leukemic cells were noted in the two morphologic subtypes of acute promyelocytic leukemia. Fewer patients with M3V tended to enter complete remission (65% vs. 80%; P= .20), but no significant differences were found in the duration of complete remission (P= .81; 1 year rate, 50% vs. 85Y0), or probability of survival (P= .67; 1 year rate, 49% vs. 68Yo).
π SIMILAR VOLUMES
## BACKGROUND. Extramedullary acute promyelocytic leukemia (APL) is rare, and said to be more common after treatment with all-trans retinoic acid (ATRA) than after any other treatment. ## METHODS. The case of a child with extramedullary relapse of APL after initial treatment with ATRA and that
Because extramedullary depositions of APL are uncommon, information concerning the therapeutic Department of Orthopaedics University Ho Λpital H. Mondor role of ATRA in extramedullary disease is insufficient. In their article, Wiernik et al. state that at least one Creteil, France Gaetano Bacci, M.D