Nishio Hajime, Sato Takako, Fukunishi Shinya, Tamura Akiyoshi, Iwata Misa, Tsuboi Kento, Suzuki Koichi
Department of Legal Medicine, Osaka Medical College, 2-7 Daigaku, Takatsuki 569-8686, Japan.
Leg Med (Tokyo). 2009 May;11(3):142-3. doi: 10.1016/j.legalmed.2008.12.004. Epub 2009 Feb 14.
Malignant hyperthermia (MH) is a genetic disorder of skeletal muscle in susceptible individuals that is triggered by exposure to anesthetic agents, and can cause death. Mutations in the ryanodine receptor type 1 gene (RYR1) are associated with MH-susceptibility. MH is also triggered in susceptible individuals by severe exercise in hot conditions or by overheating in infants. Here, we report a case of a child, 2years, 9months of age, who was left in a car and exposed to a high environmental temperature. The child was suspected to have died of heat stroke by autopsy examinations. Postmortem mutation analysis revealed that the child possessed two distinct RYR1 mutations. Since each mutation had previously been identified in a separate MH-susceptible patient, MH-susceptibility with over-response to the environmental high temperature might have occurred in this child with RYR1 mutations. These findings suggest that a MH-susceptible case may have died with a presumed diagnosis of heat stroke at autopsy.
恶性高热(MH)是一种发生于易感个体的骨骼肌遗传性疾病,由接触麻醉剂引发,可导致死亡。1型兰尼碱受体基因(RYR1)突变与MH易感性相关。在易感个体中,炎热环境下的剧烈运动或婴儿过热也可引发MH。在此,我们报告一例2岁9个月大的儿童病例,该儿童被遗留在车内并暴露于高温环境中。尸检检查怀疑该儿童死于中暑。死后突变分析显示该儿童存在两种不同的RYR1突变。由于此前在不同的MH易感患者中分别鉴定出了每种突变,该携带RYR1突变的儿童可能发生了对环境高温反应过度的MH易感性。这些发现提示,尸检时可能会将一例MH易感病例误诊为中暑死亡。