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一名年轻女性罕见的胸段脂肪脊髓脊膜膨出病例报告

A rare case of thoracic lipomyelomeningocele in a young female: A case report.

作者信息

Sharma Suraj, Khadka Hensan, Aryal Sajiva

机构信息

Bir Hospital, Mahaboudha, Kathmandu, Nepal.

Kathmandu Medical College, Kathmandu, Nepal.

出版信息

Radiol Case Rep. 2023 Jan 5;18(3):1372-1375. doi: 10.1016/j.radcr.2022.10.042. eCollection 2023 Mar.

Abstract

Thoracic lipomyelomeningocele is a rare type of congenital occult spinal dysraphism. It is characterized by lipomatous tissue connected to the dorsal spinal cord that protrudes through a spinal defect together with the meninges or spinal cord to form a posterior mass beneath the skin. Closed spinal dysraphism can present diagnostic challenges when resources are scarce and advanced imaging techniques like magnetic resonance imaging are not readily available. Here, we describe a case of thoracic lipomyelomeningocele, a type of closed spinal dysraphism in a young female presenting with gradually progressive weakness and tingling sensation in bilateral lower limbs over the last 6 months. On physical examination, she had a soft tissue swelling with dimpling over the dorsal spine and paraparesis. Magnetic resonance imaging of the spine revealed dorsal lipomyelomeningocele corresponding to D4-D7 vertebral levels with tethered spinal cord.

摘要

胸段脂肪脊髓脊膜膨出是一种罕见的先天性隐性脊柱裂。其特征是与脊髓背侧相连的脂肪组织通过脊柱缺损与脑膜或脊髓一起突出,在皮下形成一个后部肿块。当资源稀缺且磁共振成像等先进成像技术难以获得时,闭合性脊柱裂可能会带来诊断挑战。在此,我们描述一例胸段脂肪脊髓脊膜膨出病例,这是一种闭合性脊柱裂,发生在一名年轻女性身上,她在过去6个月中出现双侧下肢逐渐加重的无力和刺痛感。体格检查时,她的背部脊柱有软组织肿胀伴酒窝样凹陷及双下肢轻瘫。脊柱磁共振成像显示对应于D4 - D7椎体水平的背侧脂肪脊髓脊膜膨出伴脊髓拴系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4937/9931526/fa133cfc9bca/gr1.jpg

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