Rare additional chromosomal abnormalities in acute promyelocytic leukaemia resulting in rapidly fatal disease: report of a case
Background Acute promyelocytic leukaemia results from reciprocal translocation between
the long arms of chromosomes 15 and 17. This translocation leads to the formation of …
the long arms of chromosomes 15 and 17. This translocation leads to the formation of …
Acute Promyelocytic Leukemia with t (2; 3): An Unusual Additional Chromosomal Abnormality
S Gajendra, AK Yadav, M Bhargava - Indian Journal of Hematology and …, 2022 - Springer
Acute promyelocytic leukemia is a distinct subset of acute myeloid leukemia with
characteristic clinical, morphological and genetic features. The gene product PML-RAR …
characteristic clinical, morphological and genetic features. The gene product PML-RAR …
Persistent hypoplastic acute promyelocytic leukemia with a novel chromosomal abnormality of 46, XY, t (15; 17), t (9; 11)(q13; p13)
K Yamamoto, T Kodaka, H Maruoka… - Journal of Clinical and …, 2015 - jstage.jst.go.jp
A diagnosis of acute promyelocytic leukemia (APL) is usually made when normal
hematopoietic cells are substituted by APL cells. We encountered a unique APL patient who …
hematopoietic cells are substituted by APL cells. We encountered a unique APL patient who …
Acute promyelocytic leukemia: morphological and clinical features.
R Invernizzi, AM Iannone, S Bernuzzi, A d'Alessio… - …, 1993 - europepmc.org
Results Three morphological categories were present: a classic hypergranular type (30
cases), a microgranular type (6 cases) and a form with basophilic granules (M3b) that …
cases), a microgranular type (6 cases) and a form with basophilic granules (M3b) that …
[PDF][PDF] Acute promyelocytic leukemia microgranular variant–A clinical and therapeutical approach
M DERVESTEANU, M ONISAI, H BUMBEA… - Mædica A Journal of …, 2007 - academia.edu
Acute promyelocytic leukemia (APL) is a rare form of acute myeloid leukemia with a
particular diagnosis and therapeutic approach. APL represents only 10-15% of acute …
particular diagnosis and therapeutic approach. APL represents only 10-15% of acute …
CD34 positive-microgranular variant of acute promyelocytic leukemia in a child
AR Nargund, GV Patil, CP Raghuram… - Indian Journal of …, 2012 - journals.lww.com
Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia (AML) in which
abnormal promyelocytes predominate. APL is rare in children (approximately 10% of …
abnormal promyelocytes predominate. APL is rare in children (approximately 10% of …
[HTML][HTML] Atypical morphology and aberrant immunophenotypic expression: a diagnostic dilemma in acute promyelocytic leukemia
S Verma, P Singhal, S Singh, S Das - Journal of Applied …, 2022 - journals.lww.com
Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia, which is highly
aggressive, yet the most curable. It is a medical emergency that requires a very high index of …
aggressive, yet the most curable. It is a medical emergency that requires a very high index of …
A hypogranular variant of acute promyelocytic leukaemia showing a heterogenic immunophenotype with CD34, CD2, HLA-DR positivity: a case report and review of …
L Patteet, K Vermeulen, K Pieters… - Acta Clinica …, 2012 - Taylor & Francis
We report the case of a 46-year-old man who presented with the hypogranular variant of an
acute promyelocytic leukaemia (APL). RT-PCR analysis for detection of the t (15; 17) fusion …
acute promyelocytic leukaemia (APL). RT-PCR analysis for detection of the t (15; 17) fusion …
Acute promyelocytic leukemia: clinico-demographic profile
N Altaf, S Khan, K Abdullah, L Gul - International Journal of …, 2018 - jpathology.com
Acute promyelocytic leukemia is a unique subtype of acute Myeloid Leukemia about which
there is limited data from Pakistan. The aim of the present study is to evaluate itsclinico …
there is limited data from Pakistan. The aim of the present study is to evaluate itsclinico …