Ackerman Laurie L, Menezes Arnold H
Department of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City 52242, USA.
Pediatrics. 2003 Sep;112(3 Pt 1):641-7. doi: 10.1542/peds.112.3.641.
Dermal sinus tracts are an uncommon form of spinal dysraphism often presenting in childhood with skin findings, neurologic deficit, or infection. We reviewed our surgical experience, examining presenting symptomatology, operative findings, and patient outcomes.
A retrospective analysis of operated dermal sinus tract cases by the senior author (A.H.M.) from 1970 to present was made.
Twenty-eight patients were identified; 17 female and 11 male. Five cervical, 4 thoracic, 9 lumbar, and 9 lumbosacral tracts were explored. Sixteen patients presented at <1 year of age, and 12 were >1 year. Reasons for referral included cutaneous findings (15), neurologic deficit (8), foot abnormalities (4), infection (3), pain (2), and scoliosis (1). Our initial examination revealed cutaneous findings (eg, sinus ostea, pigmentation changes, erythema, skin tags, subcutaneous masses) in 27 patients and neurologic deficit in 19. Age-related differences were apparent. Patients >1 year were more likely to have neurologic deficit (92%) as compared with those <1 year (50%). Bifid spinous processes were noted at dural tract entry in 17 patients. Twenty-two tethered cords, 14 inclusion tumors, and 6 patients with evidence of arachnoiditis were found intraoperatively. Mean follow-up was 33 months. Eleven (39%) remained neurologically intact, 12 (43%) improved, 2 (7%) were unchanged, and 3 (11%) were worse with 2 having decreased perianal sensation and 1 slightly worsened motor function postoperatively.
Although most patients were referred for cutaneous stigmata evaluation, >50% had neurologic deficit, intradural tumors, or tethered cords. Skin findings identification should initiate prompt radiologic evaluation and neurosurgical intervention with intradural exploration. Timely intervention may preserve or improve neurologic function in these patients.
皮样窦道是脊髓发育异常的一种罕见形式,常在儿童期出现皮肤表现、神经功能缺损或感染。我们回顾了我们的手术经验,研究了临床表现、手术发现和患者预后。
对资深作者(A.H.M.)自1970年至今手术治疗的皮样窦道病例进行回顾性分析。
共确定28例患者;17例女性,11例男性。探查了5例颈段、4例胸段、9例腰段和9例腰骶段窦道。16例患者在1岁前就诊,12例患者在1岁后就诊。转诊原因包括皮肤表现(15例)、神经功能缺损(8例)、足部异常(4例)、感染(3例)、疼痛(2例)和脊柱侧弯(1例)。我们的初步检查发现27例患者有皮肤表现(如窦口、色素沉着改变、红斑、皮赘、皮下肿块),19例有神经功能缺损。年龄相关差异明显。1岁以上患者神经功能缺损的发生率(92%)高于1岁以下患者(50%)。17例患者在硬脊膜窦道入口处可见双裂棘突。术中发现22例脊髓栓系、14例包涵体肿瘤和6例有蛛网膜炎证据的患者。平均随访33个月。11例(39%)神经功能保持完好,12例(43%)有所改善,2例(7%)无变化,3例(11%)病情恶化,其中2例术后肛周感觉减退,1例运动功能略有恶化。
尽管大多数患者因皮肤体征评估而转诊,但超过50%的患者存在神经功能缺损、硬脊膜内肿瘤或脊髓栓系。发现皮肤表现应立即进行影像学评估并进行硬脊膜内探查的神经外科干预。及时干预可能会保留或改善这些患者的神经功能。