Hasegawa H, Bitoh S, Tamura K, Obashi J
Department of Neurosurgery, Osaka Koseinenkin Hospital, Japan.
No Shinkei Geka. 1989 May;17(5):481-4.
A rare case of idiopathic massive osteolysis of the skull is reported. A 49 year-old male was admitted with a diagnosis of a skull tumor. The skull film taken for evaluation of the headache, showed a large lytic lesion with irregular margin in the left parietal area. CT showed that some of the bone had been destroyed, but the underlying brain was normal. Technetium 99m-MDP bone scan showed high activity around the margin of the lytic lesion. During surgery for this bone lesion no neoplastic or inflammatory changes were revealed. However, destruction of the bone without new bone formation could be seen. Idiopathic massive osteolysis of skull bone is extremely rare and the authors could find only 6 reported cases in the literature. It is characterized by the spontaneous onset of bone resorption without known causative factors. This destructive process continues for years until eventually it ceases spontaneously. In the case of skull lesion, there seems to be no need for surgery unless both the inner and outer tables are involved. This disease must be included in the differential diagnosis of lytic skull lesion.
报告了一例罕见的特发性颅骨大块骨质溶解症。一名49岁男性因颅骨肿瘤诊断入院。为评估头痛而拍摄的颅骨平片显示左顶叶区域有一个边界不规则的大溶骨性病变。CT显示部分骨质已被破坏,但下方的脑组织正常。锝99m - MDP骨扫描显示溶骨性病变边缘周围放射性增高。在对该骨病变进行手术时,未发现肿瘤性或炎症性改变。然而,可以看到骨质破坏而无新骨形成。特发性颅骨大块骨质溶解症极为罕见,作者在文献中仅能找到6例报告病例。其特点是在无已知病因的情况下自发出现骨质吸收。这种破坏过程会持续数年,直至最终自行停止。对于颅骨病变,除非内板和外板均受累,似乎无需手术。本病必须列入溶骨性颅骨病变的鉴别诊断。