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L-天冬酰胺酶治疗期间胶原诱导的血小板聚集选择性缺乏。

Selective deficiency in collagen-induced platelet aggregation during L-asparaginase therapy.

作者信息

Shapiro R S, Gerrard J M, Ramsay N K, Nesbit M E, Coccia P F, Stoddard S F, Plow E F, White J G, Krivit W

出版信息

Am J Pediatr Hematol Oncol. 1980 Fall;2(3):207-12.

PMID:6933865
Abstract

Platelet aggregation studies were performed on 10 pediatric patients with acute lymphoblastic leukemia (ALL) receiving induction therapy with vincristine, prednisone, and L-asparaginase. An isolated abnormality in platelet aggregation in response to collagen was found in all patients during the course of therapy. Platelet aggregation in response to collagen normalized following the discontinuation of L-asparaginase, while patients were still on vincristine and prednisone. In contrast to the abnormal collagen response, platelet aggregation induced by epinephrine, arachidonic acid, adenosine diphosphate (ADP), and thrombin were normal both during and following therapy. In the one patient with a normal platelet count before therapy, aggregation induced by all agents was normal. This selective abnormality in collagen aggregation therefore appears to result from therapy, with the use of L-asparaginase in particular being implicated.

摘要

对10名接受长春新碱、泼尼松和L-天冬酰胺酶诱导治疗的急性淋巴细胞白血病(ALL)儿科患者进行了血小板聚集研究。在治疗过程中,所有患者均发现对胶原的血小板聚集存在孤立异常。在停用L-天冬酰胺酶后,尽管患者仍在使用长春新碱和泼尼松,但对胶原的血小板聚集恢复正常。与异常的胶原反应相反,肾上腺素、花生四烯酸、二磷酸腺苷(ADP)和凝血酶诱导的血小板聚集在治疗期间及之后均正常。在治疗前血小板计数正常的1名患者中,所有试剂诱导的聚集均正常。因此,这种胶原聚集的选择性异常似乎是由治疗引起的,尤其与使用L-天冬酰胺酶有关。

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