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脊髓背侧皮样窦道:21例经验

Spinal dorsal dermal sinus tract: An experience of 21 cases.

作者信息

Singh Ishwar, Rohilla Seema, Kumar Prashant, Sharma Saurabh

机构信息

Department of Neurosurgery, Pt. B.D. Sharma University of Health Sciences, Rohtak, Haryana, India.

Department of Radiodiagnosis, Pt. B.D. Sharma University of Health Sciences, Rohtak, Haryana, India.

出版信息

Surg Neurol Int. 2015 Oct 7;6(Suppl 17):S429-34. doi: 10.4103/2152-7806.166752. eCollection 2015.

Abstract

BACKGROUND

Spinal dorsal dermal sinus is a rare entity, which usually comes to clinical attention by cutaneous abnormalities, neurologic deficit, and/or infection. The present study was undertaken to know the clinical profile of these patients, to study associated anomalies and to assess the results of surgical intervention.

METHODS

Medical records of 21 patients treated for spinal dorsal dermal sinus from September 2007 to December 2013 were reviewed.

RESULTS

We had 21 patients with male: female ratio of 13:8. Only 2 patients were below 1-year of age, and most cases (15) were between 2 and 15 years (mean age = 8.2 years). Lumbar region (11 cases) was most frequently involved, followed by thoracic (4 cases), lumbosacral, and cervical region in 3 patients each. All of our patients presented with neurological deficits. Three patients were admitted with acute meningitis with acute onset paraplegia and had intraspinal abscess. The motor, sensory, and autonomic deficits were seen in 14, 6, and 8 patients, respectively. Scoliosis and congenital talipes equinovarus were the common associated anomalies. All patients underwent surgical exploration and repair of dysraphic state and excision of the sinus. Overall, 20 patients improved or neurological status stabilized and only 1 patient deteriorated. Postoperative wound infection was seen in 2 cases.

CONCLUSIONS

All patients with spinal dorsal dermal sinuses should be offered aggressive surgical treatment in the form of total excision of sinus tract and correction of spinal malformation, as soon as diagnosed.

摘要

背景

脊髓背侧皮样窦是一种罕见的疾病,通常因皮肤异常、神经功能缺损和/或感染而引起临床关注。本研究旨在了解这些患者的临床特征,研究相关异常情况,并评估手术干预的结果。

方法

回顾了2007年9月至2013年12月期间接受脊髓背侧皮样窦治疗的21例患者的病历。

结果

我们有21例患者,男女比例为13:8。只有2例患者年龄在1岁以下,大多数病例(15例)年龄在2至15岁之间(平均年龄=8.2岁)。腰椎区域(11例)受累最为频繁,其次是胸椎(4例),腰骶部和颈部各有3例患者。我们所有的患者都有神经功能缺损。3例患者因急性脑膜炎伴急性发作性截瘫入院,并有椎管内脓肿。运动、感觉和自主神经功能缺损分别见于14例、6例和8例患者。脊柱侧弯和先天性马蹄内翻足是常见的相关异常情况。所有患者均接受了手术探查、修复脊柱裂状态并切除窦道。总体而言,20例患者病情改善或神经状态稳定,只有1例患者病情恶化。术后伤口感染2例。

结论

所有脊髓背侧皮样窦患者一经诊断,应尽早接受积极的手术治疗,即彻底切除窦道并矫正脊柱畸形。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84a8/4604646/dc2e70fbada5/SNI-6-429-g001.jpg

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