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Long-term outcome of isolated thrombocytopenia accompanied by hypocellular marrow
Korean Journal of Hematology ; : 128-134, 2011.
Artigo em Inglês | WPRIM | ID: wpr-720300
ABSTRACT

BACKGROUND:

Hypocellularity of bone marrow (BM), not associated with significant dyshematopoiesis, is often found in patients with isolated thrombocytopenia, but its clinical implications have not been studied. We prospectively studied the clinical features and natural history of these patients.

METHODS:

Adults with isolated thrombocytopenia (platelet counts 50x10(9)/L in 16 patients (80%). BM cellularity ranged from 5% to 25% (median, 15%) and was 150x10(9)/L) after 12, 56 and 66 months. Three patients developed pancytopenia after 11, 70 and 90 months. Two patients were consistent with moderate aplastic anemia, and 1 was confirmed as having refractory cytopenia with multilineage dysplasia. In the remainder of the patients, platelet counts remained unchanged.

CONCLUSION:

Isolated thrombocytopenia accompanied by hypocellular marrow encompasses a group of heterogeneous conditions.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Pancitopenia / Contagem de Plaquetas / Trombocitopenia / Medula Óssea / Síndromes Mielodisplásicas / Estudos Prospectivos / Seguimentos / Aberrações Cromossômicas / Púrpura Trombocitopênica Idiopática / História Natural Tipo de estudo: Estudo observacional / Estudo prognóstico / Fatores de risco Limite: Adulto / Idoso / Humanos / Masculino Idioma: Inglês Revista: Korean Journal of Hematology Ano de publicação: 2011 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Pancitopenia / Contagem de Plaquetas / Trombocitopenia / Medula Óssea / Síndromes Mielodisplásicas / Estudos Prospectivos / Seguimentos / Aberrações Cromossômicas / Púrpura Trombocitopênica Idiopática / História Natural Tipo de estudo: Estudo observacional / Estudo prognóstico / Fatores de risco Limite: Adulto / Idoso / Humanos / Masculino Idioma: Inglês Revista: Korean Journal of Hematology Ano de publicação: 2011 Tipo de documento: Artigo