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病例报告:一名新生儿患者的颈椎和胸椎存在双重皮窦道,与先天性颅内病变(脑积水和大脑半球间囊肿)相关。

Case report: double dermal sinus tracts of the cervical and thoracic spine associated with congenital intracranial pathology (hydrocephalus and an interhemispheric cyst) in a newborn patient.

机构信息

Neurosurgery Department, Juan P. Garrahan Hospital, Buenos Aires, Argentina.

Neurosurgery Department, Hospital Provincial Petrona V. de Cordero de San Fernando, Buenos Aires, Argentina.

出版信息

Childs Nerv Syst. 2023 Jun;39(6):1673-1677. doi: 10.1007/s00381-023-05865-9. Epub 2023 Feb 2.

Abstract

INTRODUCTION

A dermal sinus tract (DST) is an uncommon type of spinal dysraphisms characterized by a tract lined with stratified squamous epithelium that extends from the subcutaneous tissue to the underlying thecal sac or neural tube. These developmental anomalies can present asymptomatically with cutaneous abnormalities or with devastating complications. Usually, it is presented as a unique lesion, and there are only a few reports that show multiple sinuses, and none of them associated with midline brain malformations.

METHODS

We present the case of a 3-day-old girl with an antenatal diagnosis of hydrocephalus who was diagnosed with double dermal sinus tracts of the cervical and thoracic regions at admission. The patient presented signs of elevated intracranial pressure (ICP), which imposed a challenge in the management of the case.

RESULTS

Our patient was successfully treated initially with a lumbar puncture in order to discard a cerebrospinal fluid (CSF) infection. With negative CSF cultures, a ventriculoperitoneal shunt (VPS) was placed. Nine days after the VPS surgery and without signs of infection, the DST was excised in a single procedure, without follow-up complications.

CONCLUSION

To our knowledge, this is the first description of a patient with multiple midline neural tube defects (NTDs) associated with congenital intracranial pathology. Although there are no guidelines regarding the best treatment for this complex associated pathology, the patient was treated, without follow-up complications.

摘要

引言

皮窦道(DST)是一种罕见的脊柱发育畸形类型,其特征为一条由复层鳞状上皮衬里的管道,从皮下组织延伸到下面的硬脊膜囊或神经管。这些发育异常可以无症状出现皮肤异常,也可以出现毁灭性的并发症。通常,它表现为一个独特的病变,只有少数报告显示多个窦道,且均与中线脑畸形无关。

方法

我们报告了一例 3 天大的女孩,产前诊断为脑积水,入院时诊断为颈胸区双皮窦道。患者表现出颅内压升高(ICP)的迹象,这对病例的处理提出了挑战。

结果

我们的患者最初通过腰椎穿刺成功治疗,以排除脑脊液(CSF)感染。CSF 培养阴性后,放置脑室-腹腔分流管(VPS)。VPS 手术后 9 天,在没有感染迹象的情况下,一次性切除了 DST,没有后续并发症。

结论

据我们所知,这是首例描述伴有先天性颅内病变的多发性中线神经管缺陷(NTD)患者。尽管对于这种复杂的相关病变没有最佳治疗指南,但患者得到了治疗,没有后续并发症。

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