Rare Case of Lumbosacral Conjoint Root Diagnosed as Sequestered Disc by MRI: A Case Report

A. Awadallah
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Abstract

Introduction: Conjoint nerve root is embryological nerve root abnormality mainly affecting lumbosacral region. The atypical roots present primarily as a bifid, conjoined structure originating from a wide area of the dura. The conjoint roots are highly liable to trauma due to their size and attachment to surrounding structures. The effects of compression and entrapment are augmented in the case of having stenosis of the lateral recesses where developmental changes and disc herniations deplete the available reserve space. Conjoined nerve roots are a relatively uncommon finding but are frequently left undiagnosed on preoperative imaging studies. Misinterpretation as sequestered disc can lead to devastating results especially during limited spine approach. Case Report: A 43-year-old male patient presented with low back pain gradually progressing over the last three years. Pain was radiating to his left leg associated with tingling sensation and a mild weakness in his left foot. Clinical examination revealed normal muscle bulk and tone. Strength was full bilaterally except the mild weakness 3/5 on toe dorsiflexion of the left foot. Deep tendon reflexes were 3+ at the left knee and ankle. Plantar responses were flexor. Sensation was intact, and there was no loss of sphincters control or bladder dysfunction. A standard plain lumbosacral MRI was performed. The patient was admitted for L5/S1 discectomy. Surgical intervention was recommended, during the surgery we recognized the huge conjoint root. Adhesiolysis and discectomy was done carefully without causing any serious neural injury to the conjoint root. Clinical surgical outcome was good. Pain and tingling sensation disappeared only paresthesia over the S1 dermatome. Postoperative course was uneventful, and the patient was discharged after his neurological improvement on day 7, post operation. However, the patient complained of recurrent pain on follow-up visit and continues being followed-up. Conclusion: The conjoined nerve root anomaly diagnosis is not easy and has several points of significance. If misdiagnosed, it could be incorrectly treated as a case for a herniated disc. Neurosurgeons should consider these anomalies in their differential diagnosis. Cases of conjoined nerve root anomaly may be wrongly managed and result in wrong level of surgery with a poor outcome. Researchers conclude that the correct diagnosis of root anomalies is vital for the patient, any misinterpretation could lead to catastrophic consequences.
罕见腰骶关节根MRI诊断为隐匿性椎间盘1例
关节神经根是主要影响腰骶部的胚胎神经根异常。非典型根主要表现为起源于硬脑膜大面积的两裂连体结构。由于关节根的大小和与周围结构的附着性,它很容易受到创伤。在侧隐窝狭窄的情况下,由于发育变化和椎间盘突出耗尽了可用的储备空间,压缩和夹持的影响会增加。联合神经根是一种相对罕见的发现,但经常在术前影像学检查中未被诊断。误解为隔离椎间盘可导致毁灭性的结果,特别是在有限的脊柱入路。病例报告:一个43岁的男性病人提出腰痛逐渐进展在过去的三年。疼痛放射到他的左腿,并伴有刺痛感和左脚轻微无力。临床检查显示肌肉体积和张力正常。除了左脚脚趾背屈3/5的轻度无力外,双侧力量完全。左膝和踝关节深腱反射均为3+。足底反应为屈肌。感觉完好,没有括约肌控制丧失或膀胱功能障碍。进行标准的腰骶部MRI平扫。患者接受L5/S1椎间盘切除术。手术干预是推荐的,在手术中我们发现了巨大的联合根。粘连松解和椎间盘切除术在未对关节根造成严重神经损伤的情况下进行。临床手术效果良好。疼痛和刺痛感消失,只有S1皮节感觉异常。术后过程顺利,患者术后第7天神经系统改善出院。然而,患者在随访中抱怨复发性疼痛,并继续随访。结论:联合神经根异常诊断不易,有几点意义。如果误诊,可能会被误诊为椎间盘突出。神经外科医生在鉴别诊断时应考虑这些异常。连体神经根异常的病例可能处理不当,导致错误的手术水平和不良的结果。研究人员得出结论,正确诊断牙根异常对患者至关重要,任何误解都可能导致灾难性的后果。
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