颈椎疣样皮肤附着物伴连续的有限背髓裂,经长期随访后解栓治疗。

Surgical neurology international Pub Date : 2025-03-14 eCollection Date: 2025-01-01 DOI:10.25259/SNI_1094_2024
Keishi Makino, Seiji Tajiri, Ryosuke Mori, Akira Takada, Yasuyuki Hitoshi, Akitake Mukasa
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引用次数: 0

摘要

背景:局限性背髓裂(LDM)是指在初级神经管形成过程中,神经外胚层与皮肤外胚层的分离导致局部分离,导致连续的脊髓样连接和脊髓栓系。我们报告了一例宫颈LDM伴疣样皮肤附属物,经长期随访切除治疗。病例描述:患者为18岁女孩。自出生以来,在颈后可见一疣状皮肤附属物。计算机断层扫描显示颈椎和胸椎脊柱裂,脊柱磁共振成像(MRI)显示颈部皮肤病变和胸脊髓背侧硬膜囊增大。18岁时,患者偶尔出现左手麻木,由于t2加权MRI显示颈脊髓背侧出现新的高信号强度,患者被转介到我们的门诊。MRI显示颈正中皮损处连续硬脊膜内脊髓背侧有脊髓样物,同一区域有高信号。诊断为脊髓样物质引起的症状性颈脊髓栓系,患者接受了手术切除。在手术中,从皮肤病变处将束作为单个肿块切除到硬脑膜中,并在脊髓背侧解开束系。组织学诊断为假性真皮窦道,未见管腔结构或神经组织,因为索样物质为含有小血管的结缔组织。根据神经影像学和病理结果,诊断为颈椎LDM。术后神经症状得到改善。结论:在此,我们报告了一例经过长期随访治疗的宫颈LDM。手术后病人的症状立即好转。宫颈LDM是罕见的,LDM的手术时机应根据患者的情况考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cervical wart-like cutaneous appendage with a contiguous stalk of limited dorsal myeloschisis treated with untethering after long-term follow-up.

Background: Limited dorsal myeloschisis (LDM) is a condition in which the separation of the neuroectoderm from the cutaneous ectoderm during primary neural tube formation results in localized disjuncture, causing a continuous cord-like connection and spinal cord tethering. We reported a case of cervical LDM with a wart-like cutaneous appendage that was treated with excision after long-term follow-up.

Case description: The patient was an 18-year-old girl. A wart-like cutaneous appendage was noted over the nape of the neck since birth. Computed tomography showed spina bifida in the cervical and thoracic spines, and spinal magnetic resonance imaging (MRI) showed a cervical skin lesion and an enlarged dural sac in the dorsal thoracic spinal cord. At 18 years of age, the patient occasionally experienced numbness in her left hand and was referred to our outpatient clinic due to a new high signal intensity in the dorsal cervical spinal cord on a T2-weighted MRI. The MRI showed that a cord-like object was continuous intradural and dorsal to the spinal cord from a cutaneous lesion in the median cervical region, with a high signal in the same region. Symptomatic cervical spinal cord tethering due to a cord-like material was diagnosed, and the patient underwent resection. During surgery, the tract was removed from the cutaneous lesion into the dura mater as a single mass and untethered in the dorsal spinal cord. The histological diagnosis was a pseudo-dermal sinus tract with no luminal structures or neural tissue present, as the cord-like substance was connective tissue containing small blood vessels. Based on the neuroimaging and pathological findings, the patient was diagnosed with cervical LDM. Neurological symptoms improved postoperatively.

Conclusion: Herein, we reported a case of cervical LDM that was treated after long-term follow-up. The patient's symptoms improved immediately after surgery. Cervical LDMs are rare, and the timing of surgery for LDM should be considered according to the patient's condition.

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