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A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. A case report.
JabbarAl-Obaidi, M; Rymes, N; White, P; Pomfret, M; Smith, H; Starczynski, J; Johnson, R.
  • JabbarAl-Obaidi M; Department of Haematology, Birmingham Heartlands Hospital, Birmingham, UK.
Acta Haematol ; 107(2): 98-100, 2002.
Article en En | MEDLINE | ID: mdl-11919390
ABSTRACT
A 56-year-old male presented with inguinal lymphadenopathy and leucocytosis (WBC 98 x 10(9)/l). Bone marrow morphology showed myeloid hyperplasia, with eosinophilia. Cytogenetic analysis showed no evidence of the Philadelphia chromosome, and fluorescence in situ hybridisation studies for the BCR/ABL fusion were negative. All cells examined showed the t(8;13)(p11;q12) translocation. Six weeks after presentation, the disease progressed to an acute lymphoblastic leukaemia (ALL). The lymphoblasts were CD19/CD10 dual positive. Cytogenetic analysis again showed the t(8;13) translocation, with no additional abnormalities. There have been at least 14 reported cases of the t(8;13) myeloproliferative disorder to date, of which only 3 transformed to B-lineage ALL our case is the 4th.
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Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 8 / Transformación Celular Neoplásica / Linfoma de Burkitt / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans / Male / Middle aged Idioma: En Año: 2002 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 8 / Transformación Celular Neoplásica / Linfoma de Burkitt / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans / Male / Middle aged Idioma: En Año: 2002 Tipo del documento: Article