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一例罕见的巨大终丝脊髓脊膜膨出合并部分骶骨发育不全病例。

A rare case of giant terminal lipomyelocystocele with partial sacral agenesis.

作者信息

Ramdurg Shashank Ravindra, Rajshekhar S Jerwargikar, Dubey Shubhi, Odugoudar Avinash R

机构信息

Department of Neurosurgery, Basveshwara Teaching and General Hospital, Gulbarga, Karnataka, India.

出版信息

J Pediatr Neurosci. 2013 Jan;8(1):52-4. doi: 10.4103/1817-1745.111425.

Abstract

Terminal myelocystoceles (TMCs) are a rare form of occult spinal dysraphism. They constitute approximately 5% of skin covered lumbosacral masses. The TMC is composed of a low-lying conus medullaris with cystic dilatation of caudal central canal, a surrounding meningocele and a lipoma that extends from the conus to a subcutaneous fat collection. A 6-month-old female child presented with a large lumbosacral mass (14 cm × 12 cm × 10 cm) and weakness at the ankle joints since birth. Magnetic resonance imaging and computed tomography scan revealed a low-lying terminal lipomyelocystocele with holocord syrinx and partial sacral agenesis. The child was operated on successfully. This is an interesting and rare case of giant terminal lipomyelocystocoele with syrinx and a partial sacral agenesis. Terminal lipomyelocystocele should be included in the differential diagnosis of congenital lesions presenting as a lumbosacral mass and operated early.

摘要

终末脊髓脊膜膨出(TMCs)是隐性脊柱裂的一种罕见形式。它们约占腰骶部有皮肤覆盖肿物的5%。TMC由低位脊髓圆锥、尾侧中央管囊性扩张、周围的脊膜膨出以及从脊髓圆锥延伸至皮下脂肪聚集处的脂肪瘤组成。一名6个月大的女童自出生以来腰骶部有一个大肿物(14厘米×12厘米×10厘米),踝关节无力。磁共振成像和计算机断层扫描显示为低位终末脂肪脊髓脊膜膨出伴全脊髓空洞症和部分骶骨发育不全。该患儿手术成功。这是一例伴有脊髓空洞症和部分骶骨发育不全的巨大终末脂肪脊髓脊膜膨出的有趣且罕见病例。终末脂肪脊髓脊膜膨出应纳入表现为腰骶部肿物的先天性病变的鉴别诊断,并尽早进行手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f282/3680899/2d891b0a966a/JPN-8-52-g001.jpg

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