Küenzlen E, Bauer J, Bertram U, Becker T, Lampert F, Röttger P, Mueller-Eckhardt C
Blut. 1984 Jun;48(6):363-7. doi: 10.1007/BF00319964.
A case of fatal intracranial hemorrhage is reported in an eleven year old girl with acute idiopathic thrombocytopenic purpura following a viral infection. The patient was randomized to the IgG-arm of the ITP therapy study. Immunoglobulin administration was not followed by a raise of the thrombocyte count. Neither the IgG therapy nor intensive therapeutic measurements were able to prevent the fatal course of cerebral hemorrhage in this case. Pathological and immunological findings indicate that our patient suffered from a fulminant ITP which must be considered as a part of a still active viral disease.
报告了一例11岁患有急性特发性血小板减少性紫癜的女孩在病毒感染后发生致命性颅内出血的病例。该患者被随机分配到ITP治疗研究的免疫球蛋白组。给予免疫球蛋白后血小板计数并未升高。在该病例中,免疫球蛋白治疗和强化治疗措施均未能阻止脑出血的致命进程。病理和免疫学检查结果表明,我们的患者患有暴发性ITP,必须将其视为仍在活动的病毒疾病的一部分。