Chang J H, Chang J W, Park Y G, Kim T S, Kim J A, Chung S S
Department of Neurosurgery, Brain Korea 21 Project for Medical Sciences, Brain Research Institute, Yonsei University College of Medicine, Seoul, Korea.
Acta Neurochir (Wien). 2003 Oct;145(10):927-8. doi: 10.1007/s00701-003-0114-2.
A 60 year-old female presented with a non-specific headache that she had experienced for 4 years. A simple skull X-ray indicated a well-defined, lobulated and radiolucent lesion with a thin sclerotic rim involving the parietal bone (Fig. 1A). Computed tomography revealed a hypodense lesion. Magnetic resonance imaging showed a 2 cm-sized cystic lesion in the diploic space with both tabular involvement. This lesion was not enhanced by contrast agent. It was well defined and the periosteum was intact. The cyst paralleled the CSF in signal intensity on all pulse sequences. No fluid levels were detected (Fig. 1B, C, D). After the scalp was incised, a semi-translucent and light yellow- to white-coloured bony lesion was easily identified. The outer bony cortex of this lesion was slightly elevated, and the consistency was same as that of the normal skull. A craniectomy was performed and the cystic skull lesion was removed. The inner surface of this cystic lesion was intact but appeared irregular. The cystic cavity was empty and the dura did not appear to be involved. Histologically, it was a simple cystic cavity without lining epithelium, and the surrounding bony structures were normal (Fig. 1E, F). It was diagnosed as a simple bone cyst (SBC). The postoperative course was uneventful.
一名60岁女性因非特异性头痛就诊,该症状已持续4年。头颅X线平片显示顶骨有一界限清晰、分叶状、透光的病灶,周边有薄的硬化缘(图1A)。计算机断层扫描显示为低密度病灶。磁共振成像显示板障内有一个2厘米大小的囊性病灶,累及双侧颅骨板。该病灶无强化表现。边界清晰,骨膜完整。在所有脉冲序列上,该囊肿的信号强度与脑脊液相似。未检测到液平(图1B、C、D)。切开头皮后,很容易识别出一个半透明、浅黄色至白色的骨质病变。该病变的外层骨皮质略有隆起,质地与正常颅骨相同。行颅骨切除术,切除囊性颅骨病变。该囊性病变的内表面完整,但略显不规则。囊腔内无内容物,硬脑膜未受累。组织学检查显示为一个无内衬上皮的单纯性囊腔,周围骨质结构正常(图1E、F)。诊断为单纯性骨囊肿(SBC)。术后恢复顺利。