老年人原发性血小板增多症(Primary thrombocytosis in the elderly).docVIP

老年人原发性血小板增多症(Primary thrombocytosis in the elderly).doc

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老年人原发性血小板增多症(Primary thrombocytosis in the elderly) Primary thrombocytosis in the elderly Disease diagnoses; disease studies; laboratory tests; drugs; health care; medications; disease paths; operating practices; clinical theories; tools; downloads; exit systems Disease diagnosis: primary thrombocytosis in the elderly Primary thrombocytosis in the elderly Alias ICD, classification, pathogenesis, clinical manifestation, cause of disease Prevention of prognosis, epidemiology, laboratory examinations, auxiliary examinations, diagnosis, diagnosis, treatment and principles Drug related examination of complications English name Senile primary thrombocytosis Top alias Primary thrombocytosis in the elderly; senile, primary Thrombocythemia; elderly patients with primary thrombocytosis; elderly patients with idiopathic thrombocytosis; elderly with primary thrombocytosis Top No. ICD D75.2 Top classification Geriatrics Department Top Summary Primary thrombocytosis (primary) Thrombocytosis) is a clonal disorder of abnormal proliferation of megakaryocytes characterized by increased platelets, morphological and functional abnormalities. The main clinical features are significant, persistent increases in unexplained platelets, and the tendency to bleed and thrombosis. More than half of splenomegaly. 1. because the etiology of this disease is not clear, the mechanism of thrombocytosis is unclear, but it is a kind of disease with multiple thrombus accompanied by hemorrhage in clinical manifestation. The increase of blood platelet viscosity affect the viscosity is large, prone to thrombosis, although the performance for platelet count increased, but because of the abnormal proliferation of pathological platelet adhesion, platelet aggregation and release factor? Function is poor, so it is easy to bleed. 2., this disease is associated with polycythemia vera and myelofibrosis, Some of these patients can be transformed into CML, and some scholars believe it may be related to abnormal clon

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