Vallée B, Krifa H, Korbi S, Ben Hamouda M, Essadia K M
Service de Neurochirurgie, CHU de Sousse, Tunisie.
Neurochirurgie. 1991;37(1):61-6.
The authors report, after a follow-up period of two years, a case of intramedullary congenital epidermoid cyst treated surgically. The patient, a 21 year-old man, presented with a seven year history of motor disturbances of his left lower limb and more recent urinary incontinence. The diagnosis of an intramedullary tumor was provided by a myelogram and a post-myelogram CT. In the absence of a dermal sinus or vertebral dysraphic anomalies, the epidermoid nature of the mass was an operative and histological finding. The main data from the literature are commented: frequency, topography, clinical diagnosis, and radiologic or M.R.I. imaging. Intracapsular removal of the mass seems to result, as in the presently reported case, in a satisfactory outcome.
作者报告了1例经手术治疗的髓内先天性表皮样囊肿病例,随访期为两年。患者为一名21岁男性,有左下肢运动障碍7年病史,近期出现尿失禁。脊髓造影和脊髓造影后CT检查诊断为髓内肿瘤。在没有皮样窦或脊柱发育异常的情况下,肿块的表皮样性质是手术和组织学检查结果。文中对文献中的主要数据进行了评论:发生率、部位、临床诊断以及放射学或磁共振成像。如本报告病例所示,行囊内肿块切除似乎可取得满意疗效。