TY - JOUR
T1 - Caracté ristiques biologiques des LAM à cup-like nuclei, une entité rare associée à une mutation de NPM1 et de FLT3
T2 - Confusion diagnostique possible avec une leucémie aiguë promyélocytaire variant microgranulaire ; à propos de trois cas
AU - André-Kerneïs, Élisabeth
AU - Vincenot-Blouin, Anne
AU - Fouillard, Loïc
AU - Abarah, Wajed
AU - Frayfer, Jamile
AU - Cassinat, Bruno
AU - De Botton, Stéphane
AU - Saada, Véronique
PY - 2013/7/1
Y1 - 2013/7/1
N2 - We report here three cases of cup-like leukemia, a rare and underdiagnosed form of acute myeloblastic leukemia. Clinical and biological findings are relatively stereotypical : high blood cell counts, high frequency ofNPM1 and FLT3mutations and normal karyotype, and may resemble microgranular variant of acute promyelocytic leukemia because of frequent disseminated intravascular coagulation, mature phenotypic feature with low or absent expression of CD34 and HLADR and peculiar blastic morphology (proeminent nuclear invaginations). Therefore, recongnizing cup-like nuclear leukemia is important to avoid misdiagnosis of promyelocytic leukemia and should guide specific molecular analyses.
AB - We report here three cases of cup-like leukemia, a rare and underdiagnosed form of acute myeloblastic leukemia. Clinical and biological findings are relatively stereotypical : high blood cell counts, high frequency ofNPM1 and FLT3mutations and normal karyotype, and may resemble microgranular variant of acute promyelocytic leukemia because of frequent disseminated intravascular coagulation, mature phenotypic feature with low or absent expression of CD34 and HLADR and peculiar blastic morphology (proeminent nuclear invaginations). Therefore, recongnizing cup-like nuclear leukemia is important to avoid misdiagnosis of promyelocytic leukemia and should guide specific molecular analyses.
KW - Acute myeloid leukemia
KW - Cup-like
KW - FLT3 mutation
KW - NPM1 mutation
UR - http://www.scopus.com/inward/record.url?scp=84887835673&partnerID=8YFLogxK
U2 - 10.1684/hma.2013.0826
DO - 10.1684/hma.2013.0826
M3 - Article
AN - SCOPUS:84887835673
SN - 1264-7527
VL - 19
SP - 279
EP - 284
JO - Hematologie
JF - Hematologie
IS - 4
ER -