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Acquired pure megakaryocytic aplasia: a separate haematological disease entity or a syndrome with multiple causes?
Felderbauer, P; Ritter, P R; Mattern, D; Schmitz, F; Bulut, K; Ansorge, N; Schmitt-Graeff, A; Schmidt, W E; Baier, J E.
Affiliation
  • Felderbauer P; Department of Medicine I, St Josef-Hospital, Ruhr-University Bochum, Bochum, Germany. peter.felderbauer@ruhr-uni-bochum.de
Eur J Haematol ; 72(6): 451-4, 2004 Jun.
Article in En | MEDLINE | ID: mdl-15128427
ABSTRACT
We report the case of a patient with acquired pure megakaryocytic aplasia. Until today, less than 20 cases of acquired pure megakaryocytic aplasia have been reported and the disease aetiology still seems to be unclear. This report summarizes the published data concerning possible aetiologies, treatment options and outcome of patients with acquired pure megakaryocytic aplasia. Furthermore, this case report presents an example for a possible disease progression.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Thrombocytopenia / Megakaryocytes Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2004 Document type: Article Affiliation country: Alemania
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Collection: 01-internacional Database: MEDLINE Main subject: Thrombocytopenia / Megakaryocytes Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2004 Document type: Article Affiliation country: Alemania
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