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颅底骨纤维异常增殖症合并动脉瘤样骨囊肿。病例报告及文献复习。

Concomitant fibrous dysplasia and aneurysmal bone cyst of the skull base. Case report and review of the literature.

作者信息

Haddad G F, Hambali F, Mufarrij A, Nassar A, Haddad F S

机构信息

American University of Beirut, New York, N.Y., USA.

出版信息

Pediatr Neurosurg. 1998 Mar;28(3):147-53. doi: 10.1159/000028639.

Abstract

The combination of fibrous dysplasia and aneurysmal bone cyst of the skull base is extremely rare yet it should be recognized, lest the rapid growth of the lesion and the radiological picture lead to the wrong diagnosis of a malignant process. We report on a 6(1/2)-year-old patient who suffered from concomitant fibrous dysplasia and aneurysmal bone cyst of the skull base. He is still disease-free 4 years postoperatively. The treatment of choice remains early surgical removal of the maximal amount of involved bone that can safely be achieved. There is no role for radiotherapy in the treatment of these lesions. A review of the literature is included.

摘要

颅骨底部纤维发育不良与骨囊肿合并极为罕见,但应予以识别,以免病变的快速生长及影像学表现导致对恶性病变的误诊。我们报告了一名6岁半的患者,其患有颅骨底部纤维发育不良与骨囊肿。术后4年他仍无疾病复发。治疗的首选仍是早期手术切除尽可能多的安全可切除的受累骨质。放疗在这些病变的治疗中不起作用。本文还包括文献综述。

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