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中华老年骨科与康复电子杂志 ›› 2025, Vol. 11 ›› Issue (04) : 214 -221. doi: 10.3877/cma.j.issn.2096-0263.2025.04.004

脊柱专题

复杂腰骶神经根病的临床特征分析
袁伟1, 郑肖肖2, 李秀丽2, 冯新红2,()   
  1. 1100038 北京,首都医科大学附属复兴医院骨科
    2102218 清华大学北京清华长庚医院神经内科
  • 收稿日期:2024-11-25 出版日期:2025-08-05
  • 通信作者: 冯新红
  • 基金资助:
    北京市医管中心扬帆3.0医工结合培育项目(YGLX202331)

Clinical characteristics analysis of complex lumbosacral radiculopathy

Wei Yuan1, Xiaoxiao Zheng2, Xiuli Li2, Xinhong Feng2,()   

  1. 1Department of Orthopedics, Fuxing Hospital, Capital Medical University, Beijing100038, China
    2Department of Neurology, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, Beijing102218, China
  • Received:2024-11-25 Published:2025-08-05
  • Corresponding author: Xinhong Feng
引用本文:

袁伟, 郑肖肖, 李秀丽, 冯新红. 复杂腰骶神经根病的临床特征分析[J/OL]. 中华老年骨科与康复电子杂志, 2025, 11(04): 214-221.

Wei Yuan, Xiaoxiao Zheng, Xiuli Li, Xinhong Feng. Clinical characteristics analysis of complex lumbosacral radiculopathy[J/OL]. Chinese Journal of Geriatric Orthopaedics and Rehabilitation(Electronic Edition), 2025, 11(04): 214-221.

目的

探讨复杂腰骶神经根病的临床特征,以提高对该类疾病复杂病因的认识。

方法

回顾性研究,收集2018年9月至2025年1月于首都医科大学附属复兴医院和清华大学北京清华长庚医院就诊的病因明确的腰骶神经根病患者11例,系统回顾人口学信息、临床基线数据、实验室检查、神经电生理、影像资料和手术过程等资料,总结其临床特征,对其诊治过程进行分析总结。

结果

11例患者中男3例、女8例,年龄29~71岁,病程20天至5年。11例患者首发症状为单侧或非对称性腰背疼痛,逐渐出现单侧/双侧下肢局灶性疼痛,随疾病进展出现不同程度的肌无力、肌萎缩,严重者不能独立行走,合并尿便障碍。11例患者首诊均考虑腰椎退行性病变,对症处理后,症状仍加重,最终诊断均为复杂病因的腰骶神经根病。11例患者中2例布氏杆菌病感染,2例结核感染,1例带状疱疹病毒感染,上述5例患者经积极的抗布病、抗结核和抗病毒治疗,临床症状明显缓解。1例经病理证实为粘液乳头状室管膜瘤,手术切除后预后良好。1例因直肠癌复发局部浸润累及腰骶神经根,预后差。1例为宫颈癌放疗后累及腰骶神经根。3例患者经骨穿证实为血液系统疾病,其中1例套细胞淋巴瘤,1例慢性淋巴细胞白血病,1例为急性淋巴细胞白血病。

结论

腰骶神经根病作为临床常见一大类疾病,症状多样,病因复杂,其常见病因是腰椎退行性病变,复杂少见原因包括感染、血液肿瘤、盆腔肿瘤和放疗后损伤等。临床上对于常规治疗后症状仍无改善甚至加重的腰腿痛患者,要考虑复杂病因腰骶神经根病的可能,增加必要的辅助检查提高对腰骶神经根病复杂病因的认识对患者的治疗及预后十分重要。

Objective

To explore the clinical characteristics of complex lumbosacral radiculopathy in order to enhance the understanding of its complex etiology.

Methods

A retrospective study was conducted, collecting data from 11 patients with clearly diagnosed lumbosacral radiculopathy who were treated at Fuxing Hospital Affiliated to Capital Medical University and Beijing Tsinghua Changgung Hospital from September 2018 to January 2025. Demographic information, clinical baseline data, laboratory tests, neurophysiological studies, imaging data, and surgical procedures were systematically reviewed. The clinical features were summarized, and the diagnostic and treatment processes were analyzed.

Results

Among the 11 patients, 3 were male and 8 were female, with ages ranging from 29 to 71 years and disease durations from 20 days to 5 years. The initial symptom in all patients was unilateral or asymmetric low back pain, gradually progressing to unilateral/bilateral focal lower limb pain. As the disease advanced, varying degrees of muscle weakness and atrophy developed, with severe cases leading to an inability to walk independently and urinary/fecal dysfunction. All patients were initially diagnosed with lumbar degenerative disease, but symptoms worsened despite symptomatic treatment. The final diagnoses revealed complex etiologies of lumbosacral radiculopathy. Among the 11 patients, 2 had Brucellosis infection, 2 had tuberculosis infection, and 1 had herpes zoster virus infection. These 5 patients showed significant clinical improvement after active anti-Brucellosis, anti-tuberculosis, and antiviral treatments. One patient was pathologically confirmed to have a myxopapillary ependymoma, with a good prognosis after surgical resection. One patient had lumbosacral radiculopathy due to local infiltration from recurrent rectal cancer, with a poor prognosis. One patient developed lumbosacral radiculopathy after radiotherapy for cervical cancer. Three patients were diagnosed with hematologic diseases via bone marrow biopsy: 1 with mantle cell lymphoma, 1 with chronic lymphocytic leukemia, and 1 with acute lymphocytic leukemia.

Conclusions

Lumbosacral radiculopathy is a common clinical condition with diverse symptoms and complex etiologies. While lumbar degenerative disease is a common cause, complex and rare causes include infections, hematologic malignancies, pelvic tumors, and post-radiation injury. For patients with lumbosacral pain who do not improve or even worsen after conventional treatment, the possibility of complex lumbosacral radiculopathy should be considered. Increasing the use of necessary auxiliary examinations to improve the understanding of complex etiologies is crucial for patient treatment and prognosis.

表1 11例腰骶神经根病患者的一般资料
编号 性别 年龄 既往史 首发症状 病程 体格检查(首次就诊)
1 51岁 体健 腰痛,右下肢无力 7周 双上肢肌力5级,双下肢近端及足背屈肌力3-级,跖曲4级;四肢腱反射未引出,肛门反射、腹壁反射消失;双侧病理征未引出。双侧大腿、小腿外侧及足底针刺觉及触觉减退,鞍区感觉减退
2 71岁 高血压 双髋及腰部疼痛伴下肢无力疼痛 20天 双上肢肌力V级,双下肢因腰部疼痛不敢用力,但无明显偏侧力弱,肌张力正常。双侧腱反射正常,双侧Hoffmann征阴性,双侧病理征阳性
3 56岁 腰椎间盘突出 腰痛伴双下肢麻木行走无力 5年 左下肢伸髋、屈髋、伸膝、屈膝肌力4级,足背屈、跖屈肌力2级,右下肢近远端肌力4级,双上肢及右下肢腱反射活跃,左侧膝反射未引出,左侧掌颌反射阳性,双侧Hoffmann征、Rossolimo征及Chaddock征阳性。左膝以下深浅感觉减退
4 62岁 肠癌术后,粒子植入治疗,放疗后 腰痛右下肢无力 6个月 双上肢肌力及左下肢肌力5级,右下肢肌力差,曲髋、伸膝、大腿外展4-级,足背屈跖曲5级,大腿前侧针刺觉减退,双侧病理征未引出
5 54岁 体健 双腹股沟区疼痛,放射至双下肢,伴下肢麻木、活动不利 2月 双下肢近端肌力5-级,四肢腱反射对称(+),双侧病理征未引出,针刺觉未见异常
6 64岁 腰椎间盘突出 腰骶部及右侧腰背部疼痛,活动后加剧,伴有右下肢放射痛 5年加重1个月 腰段棘突及右侧椎旁压痛、叩痛(+),脊柱活动明显受限,双侧直腿抬高试验及加强试验(-),股神经牵拉试验(-),双下肢踝背伸肌力4级,无肌萎缩,双下肢针刺觉未见异常。右侧膝腱反射减弱,双侧病理征未引出,布氏征、克氏征均未引出
7 66岁 高血压 右下肢疼痛、无力 1月 左下肢肌力V级,右下肢屈髋肌力I级,屈膝伸膝肌力II级,跖背屈肌力IV级
8 57岁 7年前宫颈癌手术后放化疗 双大腿前侧,臀部僵硬感、酸痛 5年 四肢肌力5级,腱反射未引出,针刺觉未见异常
9 72岁 体健 腰痛,双下肢无力伴四肢麻木 7周 双上肢肌力5级,下肢近端肌力3级,远端5级,腱反射未引出,针刺觉未见异常
10 64岁 体健 单侧起病,右髋部及右大腿酸胀感,双足发麻,逐渐出现双下肢无力 1个月 双下肢肌力I级,膝腱反射、跟腱反射未引出,病理征(-)。感觉:双侧踝部以远针刺觉过敏,左下肢音叉振动觉减退,双下肢关节位置觉减退
11 29岁 体健 腰骶部及右下肢疼痛 1个月 左下肢屈髋、伸髋、髋外展及内收、屈膝伸膝为5级,足背屈2级、跖屈4级;伸趾2级、屈趾4级;右下肢屈髋、伸髋、髋外展及内收、屈膝伸膝为4级,足背屈2级、跖屈4级;伸趾2级、屈趾4级;双下肢腱反射未引出,病理征未引出;深浅感觉未见异常
表2 11例腰骶神经根病患者神经电生理资料、影像资料、最终诊断、治疗和预后
病例 性别 最终诊断 神经电生理检查 影像学检查 确诊方式 治疗 预后
1 结核性腰骶神经根病 双下肢神经源性损害(L4、L5、S1水平) 胸椎磁共振:T8水平脊髓异常强化,胸椎轻度退变。腰骶椎磁共振:腰椎退行性变,L3~S1间盘膨出,腰骶神经根肿胀。PET-CT:T5~L1节段脊髓代谢性弥漫性增高。脊髓血管造影未见异常 试验性抗结核治疗 规范抗结核治疗1年半 痊愈
2 结核性脊柱感染合并腰骶神经根病 右下肢神经源性损害(L3、L4、L5水平) 腰椎增强核磁扫描可见L3、L4椎体及椎旁软组织明显强化,强化欠均匀,椎旁软组织异常信号范围较前略扩大,两侧腰大肌、右侧竖脊肌受累;L3-4椎间隙变窄,间盘明显强化 试验性抗结核治疗 规范抗结核治疗1年半 痊愈
3 布氏杆菌脊髓神经根神经炎合并腰椎管狭窄 双下肢神经源性损害(左L4、L5、S1水平,右侧L5 腰椎退行性变,L3~S1间盘膨出、突出,继发椎管狭窄;腰椎管内脊膜多发增厚,感染性病变可能大 血和脑脊液虎红试验(+),血和脑脊液布氏杆菌IgG阳性 规范抗布病治疗1年 痊愈
4 直肠癌放疗后+局部侵犯腰骶神经丛 右下神经源性损害(腰骶丛损害) 核磁结果:"直肠癌术后、左下腹造瘘术"后右侧盆壁及骶前软组织肿块,考虑复发或转移,累及膀胱右侧壁、右侧精囊腺及前列腺。右侧输尿管盆段受累,继发右侧输尿管梗阻扩张、右侧骶神经受侵可能性大 直肠癌术后病史 原发病治疗 死亡
5 套细胞淋巴瘤累及腰骶神经根 右下神经源性损害(L4、L5、S1水平) 腰骶部MRI:双侧髂骨、骶骨骨质破坏伴软组织肿块形成,考虑淋巴瘤可能性大,双侧腰骶神经根、坐骨神经近段受侵 骨髓穿刺 化疗和骨髓移植 症状稳定
6 布氏杆菌性脊柱炎合并神经根病 双下肢神经源性损害(L4、L5、S1水平) MRI:提示腰椎生理曲度过曲;椎体边缘可见明显骨质增生改变;T12、L1-5椎体蝶形变,L1、2、4椎体内信号异常,ST1R呈稍高信号,L3椎体见水泥置入;T10-L3层面椎管内串珠状分布可见类圆形异常信号影,部分突入椎管内 术中穿刺液培养出布氏杆菌 规范抗布病治疗 症状明显缓解,治疗中
7 带状疱疹后腰骶神经根神经丛病 右下肢神经源性损害(腰丛损害合并L5-S1损害) 腰骶丛神经磁共振增强成像:右侧L3、L4神经根病变,右侧腰骶部肌群水肿,腰椎退变;L1-S1间盘膨出,腰骶筋膜炎。神经超声:股神经于腹股沟段部分神经束水肿。 前驱带状疱疹感染病史,排除其它 抗病毒、激素治疗 痊愈
8 宫颈癌放疗后腰骶神经根/丛病 双下肢神经源性损害(L4、L5、S1水平) 腰骶丛增强核磁:双侧腰骶丛及其分支多发节段性水肿,左侧为著,结合病史,考虑放疗后改变;盆壁皮下软组织及双侧髂肌水肿;骶骨左侧局限信号异常 病史、肌电图肌颤搐电位 未给予特殊治疗 无变化
9 慢性淋巴细胞白血病累及腰骶神经丛 双下肢神经源性损害(双侧L2-S1水平) 腰椎MRI:退行性病变,L3-4椎间盘膨出,L4-5椎间盘膨出、突出 骨髓和基因检查 化疗 症状稳定
10 急性淋巴细胞白血病累及腰骶神经丛/根病 双下肢神经源性损害(L2~S1水平) 胸腰椎增强MRI:T7-8棘突异常强化;脊髓圆锥表面、S2水平骶管内异常强化灶;腰骶丛神经增强MRI:局灶点状强化 骨髓和基因检查 TKI + VDCLP方案诱导治疗;两次鞘注 发病3个月后死亡
11 粘液乳头状室管膜瘤(WHOI级),累及腰骶神经根 双下肢神经源性损(L3、L4、L5、S1水平) 腰骶神经根增粗、丛集,病变弥漫,强化明显 手术病理 手术切除+康复锻炼 术后4月可独立行走
图12~15 病例6,腰椎退变伴明显后凸;T12、L1-5椎体楔形变,L1/2/4椎体内信号异常,L3椎体内见充填的骨水泥;T10~L3层面椎管内见串珠状分布的类圆形异常信号影,部分突入硬膜内(图12箭头)。图12T1像;图13T2像;图14抑脂像;图15T1增强核磁像
图16~21 病例11,送检组织内见少许卵圆形及立方状肿瘤细胞,呈乳头放射状排列在血管间质轴心周围,细胞轻度异型,周围见多个粗大神经束(HE)。免疫组化:GFAP(+)、S-100(+)、CD34(血管+)、Ki-67(+),病变符合粘液乳头型室管膜瘤(WHO Ⅰ级)
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