Chen C M, Liang D C, Shen E Y
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1989 Nov-Dec;30(6):389-93.
Five of 34 hemophiliac children suffered from nine episodes of intracranial hemorrhage (ICH) from hemophilia A, and another 3 were B hemophiliacs. Diagnoses were confirmed by computed tomographic scan in all nine episodes. The ages of the patients with ICH ranged from 3 months to 4 1/2 years. The most frequent presenting symptoms were headache and vomiting, followed by focal neurological deficits. Eight of 9 episodes had bleeding in multiple regions. All the patients received immediate replacement therapy had recovered without surgical intervention. The duration of treatment was 10 +/- 2 days. All the patients survived and only one of them had neurological sequela as left hand paresis. From this observation we suggest that the treatment of suspected ICH in hemophiliacs should include prompt replacement therapy for either trauma or neurological symptoms in the absence of trauma history, documentation of ICH by computed tomographic scan, and prolonged replacement therapy and control of increased intracranial pressure in hemophiliacs with documented ICH.
34名血友病儿童中有5名因甲型血友病发生了9次颅内出血(ICH),另外3名是乙型血友病患者。所有9次发作均通过计算机断层扫描确诊。发生颅内出血的患者年龄从3个月到4岁半不等。最常见的症状是头痛和呕吐,其次是局灶性神经功能缺损。9次发作中有8次在多个区域出血。所有接受立即替代治疗的患者未经手术干预均已康复。治疗持续时间为10±2天。所有患者均存活,其中只有1人有神经后遗症,即左手轻瘫。根据这一观察结果,我们建议,对于血友病患者疑似颅内出血的治疗应包括:在无创伤史的情况下,针对创伤或神经症状迅速进行替代治疗;通过计算机断层扫描记录颅内出血情况;对已记录颅内出血的血友病患者进行延长替代治疗并控制颅内压升高。