Acute leukaemia with a pure erythroid phenotype: under‐recognized morphological and cytogenetic signatures associated universally with primary refractory disease and a dismal clinical outcome
Histopathology2017Vol. 71(2), pp. 316–321
Citations Over Time
Abstract
We describe previously unreported but relatively common findings of extensive tumour necrosis and recurring cytogenetic abnormalities in ALPEP. Our findings suggest strongly that ALPEP represents a distinct clinicopathological entity regardless of its WHO classification.
Related Papers
- → Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML(2007)77 cited
- → Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group(2004)67 cited
- → Familial Acute Myeloid Leukemia with Monosomy 7(2000)26 cited
- → A Complex Translocation (5;7) in a Patient with Acute Nonlymphocytic Leukemia Evolved from a Myelodysplastic Syndrome(1998)2 cited
- → 144 Detection of telomerase activity in cell in myelodysplastic syndromes: Application of in situ telomeric repeat amplification protocol (TRAP)(1997)1 cited