Transient thrombocytosis with megathrombocytes in a case of acute myeloblastic leukemia.

Thrombocytosis is commonly seen in reactive conditions and certain neoplastic states, such as chronic myeloproliferative disorders. It is rarely seen in acute leukemia. A 12-year-old girl with acute myeloblastic leukemia (FAB M2) in remission presented with pyoderma. Her hemogram revealed anemia (Hb...

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Publicado en:Indian Journal of Pathology & Microbiology Vol. 52; no. 1; pp. 113 - 115
Autores principales: Kotru M, Batra M, Gomber S, Rusia U, Kotru, Mrinalini, Batra, Madhu, Gomber, Sunil, Rusia, Usha
Formato: case study Journal Article
Publicado: Wolters Kluwer India Pvt Ltd Jan-Mar2009
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan-Mar2009
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      pub: Wolters Kluwer India Pvt Ltd
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        atl: Transient thrombocytosis with megathrombocytes in a case of acute myeloblastic leukemia.
      aug:
        au:
          Kotru M
          Batra M
          Gomber S
          Rusia U
          Kotru, Mrinalini
          Batra, Madhu
          Gomber, Sunil
          Rusia, Usha
        affil: Department of Pathology, University College of Medical Sciences and Associated Guru Teg Bahadur Hospital, New Delhi - 110 095, India
      sug:
        subj:
          Leukemia, Myeloid, Acute Complications
          Leukemia, Myeloid, Acute Pathology
          Thrombocytosis Pathology
          Anemia Etiology
          Child
          Female
          Pyoderma Etiology
          Child: 6-12 years
          Female
      ab: Thrombocytosis is commonly seen in reactive conditions and certain neoplastic states, such as chronic myeloproliferative disorders. It is rarely seen in acute leukemia. A 12-year-old girl with acute myeloblastic leukemia (FAB M2) in remission presented with pyoderma. Her hemogram revealed anemia (Hb-6.4g/dl), leucopenia (TLC - 1.2 x 109/L) and thrombocytosis (platelet count- 580 x 109/L). A peripheral blood film showed numerous abnormally large platelets with few atypical cells. The thrombocytosis subsided with the clearance of infection but atypical cells persisted. One month later, she relapsed. Cytogenetic analysis revealed variable results (trisomy 9 and deletion 3). This case has been presented because thrombocytosis is rare in AML and its appearance calls for a close follow-up.
      pubtype: Academic Journal
      doctype:
        case study
        Journal Article
      ougenre: Article
    language: English
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