Chiari malformation type I with extensive syringomyelia presenting as progressive bilateral foot drop: a case report.

IF 1.4 Q4 PRIMARY HEALTH CARE
Siti Anisah Jamaludin, Suraya Abdul-Razak, Shalini Bhaskar, Mimi Nashra, Nik Munirah Nik Mohd Nasir, Nordini Asri
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引用次数: 0

Abstract

Chiari malformation type I (CMI) is a structural abnormality characterized by cerebellar tonsil herniation through the foramen magnum, often leading to disrupted cerebrospinal fluid dynamics and syringomyelia. While CMI commonly presents with occipital headaches and neck pain, atypical manifestations, such as bilateral foot drops, are exceedingly rare. We describe a 37-year-old female patient presenting with bilateral foot drop, which was later established to be caused by syringomyelia secondary to CMI. Magnetic resonance imaging revealed an 8 mm tonsillar descent and a syrinx extending to the conus medullaris. The patient refused surgical intervention and opted for conservative management; partial functional recovery was subsequently observed. This report emphasizes the importance of recognizing rare neurological presentations of CMI. To our knowledge, this is the first documented case of CMI with syringomyelia presenting as a bilateral foot drop.

伴有广泛脊髓空洞的I型Chiari畸形,表现为进行性双侧足下垂1例。
I型Chiari畸形(CMI)是一种结构异常,其特征为通过枕骨大孔的小脑扁桃体突出,常导致脑脊液动力学紊乱和脊髓空洞。虽然CMI通常表现为枕部头痛和颈部疼痛,但非典型表现,如双侧足下垂,是非常罕见的。我们描述了一位37岁的女性患者,表现为双侧足下垂,后来确定是由CMI继发的脊髓空洞引起的。磁共振成像显示扁桃体下降8毫米,耳鸣延伸至髓圆锥。患者拒绝手术治疗,选择保守治疗;随后观察到部分功能恢复。本报告强调了认识罕见的神经学表现的重要性。据我们所知,这是首例记录在案的CMI伴脊髓空洞表现为双侧足下垂的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Korean Journal of Family Medicine
Korean Journal of Family Medicine PRIMARY HEALTH CARE-
CiteScore
4.00
自引率
4.30%
发文量
51
审稿时长
53 weeks
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