La leucémie aiguë mégacaryoblastique, ou de type 7 (LAM7), représente 0,5 à 2 % des leucémies aiguës (LA) de l’enfant et 3 à 10 % des leucémies aiguës. Aspects épidémiologiques, cliniques, cytologiques et immunophénotypiques des leucémies aiguës chez les enfants: expérience du laboratoire d’hématologie. Disease definition. Acute myeloid leukemia (AML) is a group of neoplasms arising from precursor cells committed to the myeloid cell-line differentiation.

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AML Acute myelogenous leukemia Prevalence: Differential diagnosis includes megaloblastic anaemia, myelodysplastic syndromes, acute lymphoblastic leucemie aigue, acute biphenotypic leukemia, chronic myeloid leukemia myeloid blast phaseand metastases of tumors such rhabdomyosarcoma and neuroblastoma see these terms.

Paillard abE. Diagnosis of AML leucemie aigue relies on bone marrow aspirate or biopsy leucemie aigue the disease has been suspected. While data supporting progenitor cells committed to specific myeloid cell type has been aigie, other leucemi argue in favor for a more immature stem.

Leucémie myéloïde aiguë | Blausen Medical

We had a variety of indirect evidence for our assumption: She also developed bone and joint pain with recurrent aseptic arthritis. Leucemie aigue to the text HTML. Check this box if you wish to receive a copy of your message.

Refractory or relapsed AML is treated with a second induction course adding new drugs such gemtuzumab ozogamicin to the standard treatment. The main clinical picture leucemie aigue of a short time period with pallor, fatigue, fever, infections and hemorrhages. You can move this window by clicking on the leucemie aigue. All of them are characterized by clonal expansion of myeloid blasts.

Access to the PDF text. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: AML manifests by fever, pallor, anemia, hemorrhages and recurrent infections. Pathogenesis of AML is still unclear but a two-hit model has leucemie aigue suggested as the probable mechanism for leukemogenesis. Top of leucemie aigue page – Article Outline. Based on stratification, patients can be treated with chemotherapy consolidation leucemie aigue allogenic hematopoietic stem leucemie aigue transplantation HSCT.

Summary and related texts. Detailed information Article for general public Italiano Deutsch Diagnostic methods Diagnosis relies on laboratory findings showing anemia, thrombocytopenia and leucopenia or leukocytosis which result from disturbed hematopoietic leucemie aigue due to bone marrow and peripheral blood infiltration by immature blast cells.

Testes are usually not affected. Access to the full text of this article requires a subscription. Prognosis Prognosis varies widely according to cytogenetics, molecular findings, response to induction treatment and age, between others.

That means that AML could be the leucemie aigue of at least 2 aaigue types of gene mutations. For all other comments, please send your remarks via contact us. We report the case of a 7-month-old child who presented hepatomegaly with bicytopenia.

The documents leucemie aigue in this web site are presented for information purposes only. Mareynat eF.

Controversy is also still in the type of cell from which AML arises. Additional information Further information on this disease Classification s 2 Gene s 34 Other website s 2. Etiology Pathogenesis of AML is still unclear but a two-hit model has been suggested leucemie aigue the probable mechanism for leukemogenesis. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Other search option s Alphabetical leucemie aigue. The material is in no way intended to replace professional medical care by a qualified specialist and should not leucemie aigue used leucekie a basis for diagnosis or treatment.

Case series

Disease definition Acute myeloid leukemia AML is a group of neoplasms arising from precursor cells committed to the myeloid cell-line differentiation. You may leucemie aigue request that your data, should it be inaccurate, incomplete, unclear, outdated, not leucemie aigue used or stored, be corrected, clarified, updated or deleted.

Although, AML can occur leucemie aigue any age, it is typically a disease affecting elder people, usually more than 65 years. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Its diagnosis may be difficult because of associated myelofibrosis. leucemmie

Personal information regarding our website’s visitors, including their identity, is confidential. Prognosis of elder patients is rather poor.

Central nervous system infiltration is uncommon and mainly related with monocytic variants. Contact Help Who are we? Prognosis varies widely leucemie aigue to cytogenetics, molecular findings, response to leucejie treatment and age, between others.

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Leucémie aiguë myéloblastique peu différenciée (M0) – ScienceDirect

After morphological examination, immunophenotyping of leukemic cells, cytogenetic leucemie aigue molecular analysis should be performed. Bone and joint manifestations in leucemiie 7-month-old child.

Health care resources for this disease Expert centres Diagnostic tests Patient organisations 45 Orphan drug s