Reynoso García M, Portilla Aguilar J
Bol Med Hosp Infant Mex. 1978 May-Jun;35(3):471-9.
A clinical and statistical review of Reye's syndrome is made, reporting the case of a female seven months old infant with disturbances of the digestive tract associated to hepatomegaly, convulsive crises, maculopapular exanthema, extreme hypoglycemia, hyperammoniemia and high blood urea. The post-mortem study showed fine drop diffuse liver steatosis, renal tubuli steatosis, focal steatosis of myocardial fibers, generalized meningoencephalic edema and viral pneumonia. These clinico-pathologic characteristics lead to the diagnosis of Reye's syndrome, an infrequent entity in our milieu judged by national literature.
对瑞氏综合征进行了临床和统计学回顾,报告了一名7个月大女婴的病例,该婴儿伴有消化道紊乱,同时存在肝肿大、惊厥发作、斑丘疹、极度低血糖、高氨血症和高血尿素。尸检研究显示肝脏有细微的弥漫性脂肪变性、肾小管脂肪变性、心肌纤维局灶性脂肪变性、全身性脑膜脑炎水肿和病毒性肺炎。这些临床病理特征导致了瑞氏综合征的诊断,根据国内文献判断,这在我们的环境中是一种罕见的病症。