Tsutsumi Satoshi, Ito Masanori, Ogino Ikuko, Izumi Hiroshi, Arai Hajime, Yasumoto Yukimasa
Juntendo University, Urayasu Hospital, Department of Neurological Surgery, Urayasu, Chiba, Japan.
Turk Neurosurg. 2015;25(6):967-70. doi: 10.5137/1019-5149.JTN.12046-14.1.
A 28-year-old woman presented with complaints of severe buttock pain exacerbating for 2 weeks. Physical examination found numerous café-au-lait macules and axillary freckles. Neurological examination revealed sensory loss at the S3-S5 dermatome and significant vesicorectal dysfunction. Magnetic resonance imaging revealed an enhanced intraspinal mass at S1-S2, with bony erosion on the dorsal aspect of the sacrum. Intraoperatively, the rostral part of the tumor was found to involve a filament of the cauda equina. The tumor protruded extraspinally through an irregular-shaped defect in the dorsal dura and bony erosion. Total resection was achieved. The histological appearance was consistent with malignant peripheral nerve sheath tumor and loss of neurofibromin. Malignant peripheral nerve sheath tumor should be included in the differential diagnosis of spinal tumor in a patient with neurofibromatosis type 1.
一名28岁女性因严重臀部疼痛加剧2周前来就诊。体格检查发现多处咖啡牛奶斑和腋窝雀斑。神经学检查显示S3 - S5皮节感觉丧失及明显的膀胱直肠功能障碍。磁共振成像显示S1 - S2水平椎管内有一强化肿块,骶骨背侧有骨质侵蚀。术中发现肿瘤头端部分累及一根马尾神经纤维。肿瘤通过硬脊膜背侧不规则形缺损和骨质侵蚀向椎管外突出。实现了全切。组织学表现符合恶性外周神经鞘瘤且神经纤维瘤蛋白缺失。1型神经纤维瘤病患者发生脊柱肿瘤时,恶性外周神经鞘瘤应列入鉴别诊断。