Department of Pediatrics, Uwajima City Hospital, Uwajima, Ehime, Japan.
Neuromuscul Disord. 2013 Nov;23(11):917-21. doi: 10.1016/j.nmd.2013.06.008. Epub 2013 Sep 4.
We report a 5-year-old boy with X-linked myotubular myopathy complicated by peliosis hepatis. At birth, he was affected with marked generalized muscle hypotonia and weakness, which required permanent ventilatory support, and was bedridden for life. He died of acute fatal hepatic hemorrhage after using a mechanical in-exsufflator. Peliosis hepatis, defined as multiple, variable-sized, cystic blood-filled spaces through the liver parenchyma, was confirmed by autopsy. To avoid fatal hepatic hemorrhage by peliosis hepatis, routine hepatic function tests and abdominal imaging tests should be performed for patients with X-linked myotubular myopathy, especially at the time of using artificial respiration.
我们报告了一例 X 连锁肌小管肌病合并肝多发性血腔的 5 岁男孩。出生时,他患有明显的全身肌肉张力减退和无力,需要长期通气支持,终生卧床。他在使用机械呼吸机后因急性致命性肝出血而死亡。尸检证实肝多发性血腔是指肝实质内多个大小不一的充满血液的囊性空间。为避免 X 连锁肌小管肌病患者因肝多发性血腔导致致命性肝出血,应常规进行肝功能检查和腹部影像学检查,尤其是在使用人工呼吸时。