Posnick J C, Bortoluzzi P, Armstrong D C, Drake J M
Division of Plastic Surgery, Georgetown University Medical Center, Washington, D.C.
Plast Reconstr Surg. 1994 Apr;93(4):745-54; discussion 755-6.
From July 1987 to January 1991, 14 patients, ages 1 to 19 years (mean 6 years), were seen with nasal dermoid sinus cysts, a congenital lesion with the potential for intracranial extension. Each patient was assessed clinically for cyst location, symptoms, associated craniofacial deformity, and other congenital anomalies. In 5 (36 percent) of the 14 patients, ages 4 to 48 months (mean 25 months), computed tomographic scans indicated indirect signs of intracranial extension, which were confirmed intraoperatively and histologically in all 5 patients. After neurosurgical consultation, a combined single-stage intracranial-extracranial approach was used to excise the lesion. No perioperative complications occurred. Clinical assessment (follow-up 20 to 40 months, mean 31 months), confirmed by postoperative CT scan 1 year after surgery, indicated no evidence of recurrence, residual skeletal contour defects, or deformity; forehead and nasal growth were qualitatively normal, and scar appearance was satisfactory. Our experience indicates that intracranial extension of nasal dermoid sinus cysts seen at a tertiary care referral center are not rare, that computed tomography scan permits accurate diagnosis, and that the single-stage intracranial-extracranial approach to resection is effective and results in minimal morbidity.
1987年7月至1991年1月,我们诊治了14例年龄在1至19岁(平均6岁)的鼻皮样窦囊肿患者,这是一种有颅内扩展可能的先天性病变。对每例患者都进行了临床评估,包括囊肿位置、症状、相关颅面畸形及其他先天性异常。在14例患者中的5例(36%),年龄在4至48个月(平均25个月),计算机断层扫描显示有颅内扩展的间接征象,所有这5例患者术中及组织学检查均得以证实。经神经外科会诊后,采用联合一期颅内 - 颅外入路切除病变。围手术期无并发症发生。临床评估(随访20至40个月,平均31个月),术后1年的CT扫描证实,无复发、残留骨骼轮廓缺损或畸形的迹象;前额和鼻部生长在质量上正常,瘢痕外观令人满意。我们的经验表明,在三级医疗转诊中心所见的鼻皮样窦囊肿颅内扩展并不罕见,计算机断层扫描可做出准确诊断,一期颅内 - 颅外切除方法有效且发病率极低。