Beris P, Dunand V, Isoz C, Reynard C
Département de Médecine, Hôpital Cantonal Universitaire, Genève, Suisse.
Nouv Rev Fr Hematol (1978). 1990;32(4):277-80.
A 35 year-old HIV-positive male intravenous drug abuser developed thrombotic thrombocytopenic purpura (TTP) during the course of recto-sigmoiditis secondary to Shigella flexneri. Complete remission was achieved by aggressive treatment of a combination of plasma exchange, fresh frozen plasma infusion, continuous prostacyclin perfusion, p.o. administered aspirin-dipyridamol and intravenous injections of vincristine. During acute microangiopathy, an acquired type II von Willebrand disease was diagnosed. TTP is a newly-recognized hematologic manifestation of HIV-1 infection; endothelial damage by endotoxin during course of infection or by high serum levels of circulating immune complexes may be a causative mechanism of microangiopathy causing hemolysis and platelet consumption.
一名35岁的HIV阳性男性静脉吸毒者,在继发于福氏志贺菌的直肠乙状结肠炎病程中发生了血栓性血小板减少性紫癜(TTP)。通过血浆置换、输注新鲜冰冻血浆、持续前列环素灌注、口服阿司匹林-双嘧达莫以及静脉注射长春新碱的联合积极治疗,实现了完全缓解。在急性微血管病期间,诊断出获得性II型血管性血友病。TTP是HIV-1感染新发现的血液学表现;感染过程中内毒素或高血清水平的循环免疫复合物引起的内皮损伤可能是导致溶血和血小板消耗的微血管病的致病机制。