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急性淋巴细胞白血病中的原发性纤溶和脾脏自发性破裂

Primary fibrinolysis and spontaneous rupture of the spleen in acute lymphoblastic leukemia.

作者信息

Gafter U, Mandel E M, Weiss S, Djaldetti M

出版信息

Acta Haematol. 1976;56(6):355-9. doi: 10.1159/000207962.

Abstract

A 51-year-old male with acute lymphoblastic leukemia whose course was complicated by primary fibrinolysis and spontaneous rupture of the spleen is described. The patient was treated with various drug combinations: vincristine and prednisone, later by cytosine arabinoside and finally by prednisone, methotrexate and 6-mercaptopurine. Four months after the diagnosis he developed epistaxis and petechiae. The coagulation tests were compatible with primary fibrinolysis and he responded to treatment with epsilon-aminocaproic acid (EACA). One month and a half later he developed again epistaxis, ecchymoses, splenomegaly and an acute abdomen. The coagulation tests revealed primary fibrinolysis. The operation revealed a ruptured spleen. After splenectomy the treatment with EACA was continued and, despite an improvement in the coagulation tests, the patient died.

摘要

本文描述了一名51岁的急性淋巴细胞白血病男性患者,其病程并发原发性纤维蛋白溶解症和脾脏自发性破裂。患者接受了多种药物联合治疗:长春新碱和泼尼松,随后是阿糖胞苷,最后是泼尼松、甲氨蝶呤和6-巯基嘌呤。诊断后四个月,他出现鼻出血和瘀点。凝血检查结果与原发性纤维蛋白溶解症相符,他对ε-氨基己酸(EACA)治疗有反应。一个半月后,他再次出现鼻出血、瘀斑、脾肿大和急腹症。凝血检查显示原发性纤维蛋白溶解症。手术发现脾脏破裂。脾切除术后继续使用EACA治疗,尽管凝血检查有所改善,但患者仍死亡。

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