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骨髓增殖性疾病中的血小板功能异常。

Abnormal platelet function in myeloproliferative disorders.

作者信息

Waddell C C, Brown J A, Repinecz Y A

出版信息

Arch Pathol Lab Med. 1981 Aug;105(8):432-5.

PMID:6894852
Abstract

Platelet aggregation and circulating platelet aggregates (CPAs) were evaluated in 18 patients with myeloproliferative disorders, both with and without thrombocytosis. No specific patterns of platelet aggregation were detected, but 11 of 18 patients demonstrated abnormal aggregation to epinephrine, nine of 18 had abnormal aggregation to adenosine diphosphate, and seven of 18 had abnormal aggregation to collagen. There was no definitive correlation of bleeding episodes with abnormal aggregation. However, significant bleeding was observed in a patient with a platelet count of 1,500,000/cu mm and abnormal aggregation. The aggregation defects persisted despite lowering of platelet count. Evidence of increased circulating platelet aggregates and normal platelet aggregation was seen in two patients, one of whom had transient cerebral ischemic attacks relieved by antiplatelet therapy, with return of the CPA index to normal. In two patients with digital ischemia, claudication, and angiographic evidence of peripheral vascular disease, no laboratory evidence of increased circulating platelet aggregates was observed, but one patient had regression of symptoms with antiplatelet therapy.

摘要

对18例骨髓增殖性疾病患者(包括有血小板增多症和无血小板增多症的患者)进行了血小板聚集和循环血小板聚集体(CPA)评估。未检测到特定的血小板聚集模式,但18例患者中有11例对肾上腺素表现出异常聚集,18例中有9例对二磷酸腺苷表现出异常聚集,18例中有7例对胶原表现出异常聚集。出血发作与异常聚集之间没有明确的相关性。然而,在一名血小板计数为150万/立方毫米且聚集异常的患者中观察到了严重出血。尽管血小板计数降低,但聚集缺陷仍然存在。在两名患者中发现了循环血小板聚集体增加和血小板聚集正常的证据,其中一名患者患有短暂性脑缺血发作,经抗血小板治疗后缓解,CPA指数恢复正常。在两名患有手指缺血、间歇性跛行和外周血管疾病血管造影证据的患者中,未观察到循环血小板聚集体增加的实验室证据,但其中一名患者经抗血小板治疗后症状有所缓解。

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