Chaves-Carballo E, Montes J E, Nelson W B, Chrenka B A
Department of Neurology, Eastern Virginia Medical School, Norfolk.
Am J Dis Child. 1990 Oct;144(10):1079-82. doi: 10.1001/archpedi.1990.02150340023017.
We treated nine infants who unexpectedly developed shock, seizures, and fever, followed by diarrhea, consumption coagulopathy, and hepatorenal dysfunction. Despite vigorous treatment, three infants died and all except one of the six survivors have severe residual neurologic abnormalities. Postmortem findings included cerebral edema, white matter petechial hemorrhages, gastrointestinal hemorrhages, and fatty liver. These clinicopathologic features are similar to those previously described in 10 infants as being due to hemorrhagic shock and encephalopathy, except for the presence of fatty liver in our patients. Based on the combined experience of 19 infants, we propose diagnostic criteria for hemorrhagic shock and encephalopathy that may facilitate recognition and differentiation from other shock syndromes in infancy.
我们治疗了9名意外出现休克、惊厥和发热,随后出现腹泻、消耗性凝血病及肝肾功障碍的婴儿。尽管积极治疗,仍有3名婴儿死亡,6名幸存者中除1名外均有严重的神经功能异常后遗症。尸检发现包括脑水肿、白质瘀点出血、胃肠道出血及脂肪肝。这些临床病理特征与之前报道的10例婴儿因出血性休克和脑病所致的特征相似,只是我们的患者存在脂肪肝。基于19例婴儿的综合经验,我们提出了出血性休克和脑病的诊断标准,这可能有助于识别并与婴儿期其他休克综合征相鉴别。