Nakamura S, Katagiri T, Majima A, Wakamatsu K, Tsubokawa T, Moriyasu N
No Shinkei Geka. 1979 Apr;7(4):389-95.
A 6-year-old girl was transfered to our hospital because of continuing pleocytosis, and detection of the squamous cells and cholesterin crystals in the CSF. Neurological examination on admission revealed no remarkable disorders, except for weakness of anal sphincter. X-ray examination of the spine showed a deformity of the sacral vertebra. Myelography revealed a pre-sacral cystic tumor, which was connected with spinal CSF cavity at cul-de-sac of the spinal canal by a narrow fistula. The tumor was totally removed and no meningitic sign appeared in postoperative course. Histological examination diagnosed it as a typical epidermoid tumor. Attention should be payed to the location, size, structure and clinical course in this particular case.
一名6岁女孩因持续性脑脊液细胞增多以及脑脊液中发现鳞状细胞和胆固醇结晶而被转至我院。入院时神经系统检查除肛门括约肌无力外未发现明显异常。脊柱X线检查显示骶椎畸形。脊髓造影显示骶前囊性肿瘤,该肿瘤通过狭窄瘘管在椎管盲端与脊髓脑脊液腔相连。肿瘤被完全切除,术后病程中未出现脑膜炎体征。组织学检查诊断为典型的表皮样肿瘤。在这种特殊情况下,应注意肿瘤的位置、大小、结构和临床病程。