Giant Thoracolumbosacral Myelomeningocele: A Case Report

IF 0.3 Q4 SURGERY
Abhijit Acharya, Souvagya Panigrahi, R. Deo, S. Senapati, A. Mahapatra
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Abstract

Neural tube defects are a broad spectrum of congenital developmental anomalies that include cranial defects and open and closed spinal dysraphism. Myelomeningocele is a common form of spinal dysraphism most commonly seen in the lumbosacral region. Giant myelomeningoceles are rare occurrences. We hereby present the case of a 7-month-old infant with a history of large swelling over the thoracic lumbar region (circumference of 42 cm and diameter of 12.5 cm) that was progressively increasing in size with occasional cerebrospinal fluid (CSF) leakage from the swelling. There was associated progressive increasing size of the head size circumference (51 cm) as well for the past 6 months. There was no movement of both lower limbs since birth without any sensation up to the groin. On evaluation, the infant was found to have gross hydrocephalous. The Evans index was 0.4 with Chiari 2 malformation and a giant thoracolumbosacral myelomeningocele. The patient underwent a low-pressure ventriculoperitoneal (VP) shunt on the right side, followed by the repair of the giant myelomeningocele. The post-op period was uneventful with no CSF leakage or skin necrosis. The infant was discharged on day 5. Giant myelomeningoceles are quite a challenge for neurosurgeons due to the high risk of skin edge necrosis, CSF leaks, meningoencephalitis, etc. Here we managed our case with utmost intraoperative surgical skills and postoperative management due to which our patient was discharged in a satisfactory condition without any complication. This case is supposed to be largest myelomeningocele in the world literature to date.
巨型胸腰骶部髓母细胞瘤:病例报告
神经管畸形是一种广泛的先天性发育异常,包括颅骨缺损、开放性和闭合性脊柱发育不良。脊髓膜膨出症是脊柱发育不良的一种常见形式,最常见于腰骶部。巨型脊髓膜膨出症很少见。我们在此介绍一例 7 个月大的婴儿,其胸椎腰椎部位有一个巨大肿物(周长 42 厘米,直径 12.5 厘米),肿物逐渐增大,偶尔有脑脊液(CSF)从肿物中渗出。在过去的 6 个月里,患者的头围(51 厘米)也在逐渐增大。自出生以来,婴儿的双下肢就没有活动过,腹股沟以下也没有任何感觉。经过评估,发现婴儿患有严重的脑积水。埃文斯指数为 0.4,伴有奇亚里氏 2 型畸形和巨大胸腰骶部脊髓膜膨出。患者接受了右侧低压脑室腹腔分流术(VP),随后进行了巨大脊髓膜膨出修复术。术后情况良好,无 CSF 渗漏或皮肤坏死。婴儿于第 5 天出院。巨大脊髓膜室畸形对神经外科医生来说是一项挑战,因为极有可能发生皮肤边缘坏死、CSF渗漏、脑膜脑炎等。在本例手术中,我们运用了高超的术中手术技巧和术后处理方法,因此患者出院时情况令人满意,未出现任何并发症。该病例应该是迄今为止世界文献中最大的脊髓膜膨出病例。
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
52
审稿时长
12 weeks
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