Fuse T, Takagi T, Mizuno S, Sugino F, Fukushima T, Tan E C
Department of Neurosurgery Nagoya City Higashi General Hospital, Japan.
No To Shinkei. 1993 Sep;45(9):877-82.
We report the coexistence of multiple arteriovenous malformations (AVMs) and hemangioma of the skull in a 38-year-old man with associated varicose veins in his scalp. The patient also had hypotrophy of all right limb tissues with skin pigmentation and syndactyly of both feet. CT scans revealed intraventricular hemorrhage and a hemangioma of the skull at the posterior fossa. Because of the location of the arteriovenous malformations, surgical evacuation and resection were not attempted. The hemangioma was totally removed to decompress the posterior fossa. A few cases of regional phacomatosis with intracranial AVMs have been reported, but we could not find a report of the coexistence of intracranial multiple AVMs and hemangioma of the skull with associated varicose veins of the scalp and skeletal hypotrophy. We discuss on the etiology of the coexistence of regional phacomatosis and hemangioma and on the difference between our case and typical regional phacomatosis.
我们报告了一名38岁男性患者,其存在多发性动静脉畸形(AVM)和颅骨血管瘤,同时头皮伴有静脉曲张。该患者右下肢所有组织萎缩,伴有皮肤色素沉着和双足并指畸形。CT扫描显示脑室内出血以及后颅窝颅骨血管瘤。由于动静脉畸形的位置,未尝试进行手术清除和切除。血管瘤被完全切除以减压后颅窝。此前已有一些关于伴有颅内AVM的局部错构瘤病的病例报道,但我们未找到关于颅内多发性AVM与颅骨血管瘤并存且伴有头皮静脉曲张和骨骼萎缩的报道。我们讨论了局部错构瘤病与血管瘤并存的病因以及我们的病例与典型局部错构瘤病之间的差异。