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颈椎黄韧带血肿患者:病例报告。

A patient with cervical ligamentum flavum haematoma: case report.

机构信息

Department of Orthopedics, Zhongshan Hospital Fudan University, Shanghai, 200032, China.

出版信息

Spinal Cord Ser Cases. 2024 Aug 29;10(1):65. doi: 10.1038/s41394-024-00679-6.

Abstract

INTRODUCTION

Ligamentum flavum haematoma (LFH) is an extremely rare entity, found mostly in the lumbar and thoracic ligamentum flavum and seldom in the cervical ligamentum flavum. Cervical LFH can cause paralysis in patients. We describe a case of LFH in the cervical spine that accepted surgical treatment.

CASE PRESENTATION

A 70-year-old man with incomplete spinal cord injury presented with sudden paralysis of his left limbs for 10 days and hemi-hypaesthesia below the level of the right clavicle. Magnetic resonance imaging (MRI) showed a space-occupying lesion in the left ligamentum flavum between the C4 and C5 laminae. The preliminary diagnoses were concluded to be incomplete spinal cord injury, spinal epidural lesions, and cervical spinal stenosis. After a posterior C3-C6 laminectomy with lateral mass screw instrumentation, the muscle strength and sensation recovered partially. The lesion was greyish black and located in the ligamentum flavum. A pathological examination identified it as a haematoma of the ligamentum flavum. The patient was discharged 15 days after the operation and commenced rehabilitation.

DISCUSSION

The LFH was mainly caused by slight trauma during gentle activities and contributed by many factors. MRI is an essential tool but pathological diagnosis is the gold standard. Most LFH patients can be treated surgically.

摘要

简介

黄韧带血肿(LFH)极为罕见,多发生于胸腰椎黄韧带,颈椎黄韧带少见。颈椎 LFH 可导致患者瘫痪。我们描述了 1 例接受手术治疗的颈椎 LFH 病例。

病例介绍

1 名 70 岁男性,因左肢不完全性脊髓损伤伴 10 天突发瘫痪,右锁骨以下半身感觉减退就诊。磁共振成像(MRI)显示 C4 和 C5 椎板间左侧黄韧带占位性病变。初步诊断为不完全性脊髓损伤、硬脊膜外病变和颈椎椎管狭窄。行 C3-C6 后路椎板切除术和侧块螺钉内固定后,肌力和感觉部分恢复。病变呈灰黑色,位于黄韧带内。病理检查提示黄韧带血肿。术后 15 天患者出院并开始康复。

讨论

LFH 主要由轻微创伤在轻柔活动时引起,并与多种因素有关。MRI 是必不可少的工具,但病理诊断是金标准。大多数 LFH 患者可接受手术治疗。

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Cervical Ligamentum Flavum Hematoma: A Case Report.黄韧带血肿:一例报告。
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