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1.
East Mediterr Health J ; 16(9): 958-65, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21218723

RESUMO

This cases series describes the profile of adult patients with acute promyelocytic leukaemia (APt) at a referral hospital in Qatar. Of 34 acute myeloid leukaemia (AML) cases diagnosed, 11(32%) were classified as APt. Disseminated intravascular coagulation was common at presentation (91%). Severe thrombocytopenia was seen in 73%, leukocytosis in 55% and severe anaemia in 45%. Only 2 patients were of the classic hypergranular type. In the remaining 9 patients, 3 morphological subtypes were recognized: microgranular variant (6 patients), hyperbasophilic (2 patients) and regular nuclear outline M3r (1 patient). Translocation t(15;17) was detected in 63% of cases. APL constitutes a high proportion of AML cases in Qatar, with considerable morphological heterogeneity and a oredominance of APL variants with unfavourable oresenting features.


Assuntos
Leucemia Promielocítica Aguda/epidemiologia , Leucemia Promielocítica Aguda/patologia , Adolescente , Anemia/epidemiologia , Anemia/etiologia , Exame de Medula Óssea , Institutos de Câncer , Análise Citogenética , Feminino , Citometria de Fluxo , Variação Genética/genética , Humanos , Imunofenotipagem , Cariotipagem , Leucemia Promielocítica Aguda/classificação , Leucemia Promielocítica Aguda/etiologia , Leucocitose/epidemiologia , Leucocitose/etiologia , Masculino , Pessoa de Meia-Idade , Vigilância da População , Catar/epidemiologia , Trombocitopenia/epidemiologia , Trombocitopenia/etiologia , Translocação Genética , Adulto Jovem
2.
(East. Mediterr. health j).
em Inglês | WHO IRIS | ID: who-117987

RESUMO

This cases series describes the profile of adult patients with acute promyelocytic leukaemia [APL] at a referral hospital in Qatar of 34 acute myeloid leukaemia [AML] cases diagnosed, 11 [32%] were classified as APL. Disseminated intravascular coagulation was common at presentation [91%]. Severe thrombocytopenia was seen in 73%, leukocytosis in 55% and severe anaemia in 45%. Only 2 patients were of the classic hypergranular type. In the remaining 9 patients, 3 morphological subtypes were recognized: microgranular variant [6 patients], hyperbasophilic [2 patients] and regular nuclear outline M3r [1 patient]. Translocation t[15;17] was detected in 63% of cases. APL constitutes a high proportion of AML cases in Qatar, with considerable morphological heterogeneity and a predominance of APL variants with unfavourable presenting features


Assuntos
Leucemia Promielocítica Aguda , Imunofenotipagem , Citogenética
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