Lancinating腰椎小关节综合征:先天性小关节缺失。

IF 1.4 Q4 CLINICAL NEUROLOGY
Pain management Pub Date : 2023-10-01 Epub Date: 2023-09-29 DOI:10.2217/pmt-2023-0065
Peter D Vu, Vishal Bansal, Aila Malik, Alexa Ryder, Jason W Chen
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引用次数: 0

摘要

先天性缺失或发育不全的L5-S1小关节(关节突)是一种罕见的畸形,报告的病例不到30例。这种小关节和对侧肥大小关节的缺失提供了一系列的表现,可能使腰痛(LBP)的诊断和治疗复杂化。最初应考虑广泛的差异,包括腰椎小关节综合征、椎间盘退变、椎管狭窄、神经根突出症、脊椎关节病和骶髂关节疼痛,并灵活进行其他诊断。了解不同解剖、生物力学和生理变化对脊柱健康的影响对患者护理至关重要。我们报告了腰椎神经根病的进展,并伴有先天性缺失的左侧L5-S1小关节和肥大的右侧L5-S1关节。此外,我们的讨论集中在先天性小关节缺失的病理生理学、鉴别诊断和管理,以及它们对LBP和脊柱健康的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lancinating lumbar facet syndrome: a congenitally absent facet joint.

Congenitally absent or hypoplastic L5-S1 facet (zygapophyseal) joints are an aberrated rarity, with less than 30 reported cases. This absence of facet joint and contralateral hypertrophic facet provides a continuum of presentations that can complicate low back pain diagnoses and management. A broad differential including lumbar facet syndrome, disc degeneration, spinal stenosis, herniated radiculopathy, spondyloarthropathies and sacroiliac joint pain should be considered initially, with the flexibility for other diagnoses. Understanding the effects of different anatomical, biomechanical and physiological changes on spinal health is essential for patient care. We report a progression of lumbar radiculopathy complicated by the presence of a congenitally absent left L5-S1 facet joint and hypertrophic right L5-S1 facet joint. Furthermore, our discussion concentrates on pathophysiology, differential diagnoses and management of congenitally absent facet joints and the impact they can have on low back pain and spinal health.

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来源期刊
Pain management
Pain management CLINICAL NEUROLOGY-
CiteScore
2.90
自引率
5.90%
发文量
62
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