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骨髓增殖性疾病:体内与体外血小板功能的矛盾现象。

Myeloproliferative disorders: a paradox of in-vivo and in-vitro platelet function.

作者信息

Boughton B J, Corbett W E, Ginsburg A D

出版信息

J Clin Pathol. 1977 Mar;30(3):228-34. doi: 10.1136/jcp.30.3.228.

Abstract

A patient with features of a myeloproliferative disorder developed an acute multisystems illness and died. In-vitro platelet aggregation was imparied, but necropsy revealed widespread platelet-rich thromboemboli and multiple organ infarctions. It is suggested that platelets are damaged during disseminated intravascular platelet aggregation (DIPA) and that disaggregation of platelet thrombi and recirculation of platelets give rise to their subsequent hypofunction when tested in vitro.

摘要

一名患有骨髓增殖性疾病的患者出现急性多系统疾病并死亡。体外血小板聚集受损,但尸检发现广泛存在富含血小板的血栓栓塞和多器官梗死。有人提出,在弥散性血管内血小板聚集(DIPA)过程中血小板受到损伤,并且血小板血栓的解聚和血小板的再循环导致它们在体外检测时随后出现功能减退。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1b/476364/2acfef937469/jclinpath00161-0036-a.jpg

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