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惠普尔病中的血小板增多症。

Thrombocytosis in Whipple's disease.

作者信息

Nuzum C T, Sandler R S, Paulk H T

出版信息

Gastroenterology. 1981 Jun;80(6):1465-7.

PMID:6164596
Abstract

Three men with Whipple's disease had platelet counts of 729,000-1,142,000 per mm3, which fell to normal as their illness responded to antibiotic therapy. Reports on Whipple's disease and hospital charts from the largest published series reveal thrombocytosis in 11 of the 24 patients whose counts were recorded. The prevalence of anemia, marrow infiltration, and classic manifestations of Whipple's disease did not differ between patients with and without thrombocytosis. The thrombocytosis of Whipple's disease is similar to that of celiac sprue, Crohn's disease, and ulcerative colitis.

摘要

三名患有惠普尔病的男性血小板计数为每立方毫米729,000 - 1,142,000,随着病情对抗生素治疗产生反应,血小板计数降至正常水平。已发表的最大系列研究中的惠普尔病报告及医院病历显示,在记录了血小板计数的24例患者中,有11例出现血小板增多症。有血小板增多症和无血小板增多症的患者在贫血、骨髓浸润及惠普尔病的典型表现方面的患病率并无差异。惠普尔病的血小板增多症与乳糜泻、克罗恩病及溃疡性结肠炎的血小板增多症相似。

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