Kondo M, Hokezu Y, Yanai S, Nagamatsu K, Kida H
Department of Neurology, Oita Prefectural Hospital.
Rinsho Shinkeigaku. 1998 Jul;38(7):693-6.
We describe a rare case of a 42-year-old man with extradural spinal cord teratoma who presented with left Brown-Séquard syndrome more than 10 years after surgery for a left posterior mediastinal tumor. When he was 29 years old, he underwent an operation for a posterior mediastinal tumor. Histological findings showed adenocarcinoma in teratoma. Ten years after the operation, the patient developed left leg weakness. Three years later, he developed superficial sensory disturbance in his right leg. MRI showed extradural tumor formation at the level of the Th 9 vertebra, which compressed the spinal cord from the left posterior side. At surgery, the tumor was well encapsulated and extended to the left posterior side of the spinal cord through the intervertebral foramen. The histological findings were almost identical to those from the mediastinal tumor. This dumbbell tumor apparently developed from the remainder of the posterior mediastinal tumor over a period of more than 10 years.
我们描述了一例罕见病例,一名42岁男性患有硬膜外脊髓畸胎瘤,在接受左后纵隔肿瘤手术10多年后出现左侧布朗 - 塞卡尔综合征。他29岁时接受了后纵隔肿瘤手术。组织学检查结果显示畸胎瘤内有腺癌。术后十年,患者出现左腿无力。三年后,他右腿出现浅感觉障碍。磁共振成像(MRI)显示胸9椎体水平硬膜外肿瘤形成,从左侧后方压迫脊髓。手术时,肿瘤包膜完整,通过椎间孔延伸至脊髓左侧后方。组织学检查结果与纵隔肿瘤几乎相同。这个哑铃形肿瘤显然是在10多年的时间里由后纵隔肿瘤的残余部分发展而来。