Jones Conor, Hughes Alexander P
Orthopedic Surgery, Hospital for Special Surgery, New York, USA.
Cureus. 2024 Jul 15;16(7):e64578. doi: 10.7759/cureus.64578. eCollection 2024 Jul.
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare relapsing-remitting autoimmune polyneuropathy that targets peripheral nerves and has been associated in the literature with sarcoidosis. The goal of this study is to report the clinical case of a 61-year-old man with sarcoidosis who developed CIDP following lumbar spine surgery. The patient presented at their clinic visit with lumbar back pain and underwent a dome laminoplasty at L2-3, L3-4, and L4-5 with no known complications. Approximately four hours postoperatively, he developed bilateral lower extremity weakness most prominent along the tibialis anterior and extensor hallucis longus (L4-S1) as well as saddle anesthesia. An MRI revealed no acute changes concerning compression. Electromyography (EMG) was performed six months postoperatively, which revealed absent F waves along the peroneal and tibial nerves as well as decreased amplitude consistent with an underlying axonal neuropathy. He was referred to a neurologist for a second opinion where a diagnosis of CIDP was made. Intravenous immune globulin treatment was initiated, and the patient felt improvement in his symptoms. This case highlights the association between sarcoidosis and CIDP and discusses the pathophysiology of the disease. In patients with sarcoidosis and weakness following lumbar surgery with a negative MRI, CIDP should be on the differential.
慢性炎症性脱髓鞘性多发性神经病(CIDP)是一种罕见的复发缓解型自身免疫性多发性神经病,其病变累及周围神经,在文献中已发现它与结节病有关。本研究的目的是报告一名61岁结节病男性患者在腰椎手术后发生CIDP的临床病例。该患者因腰背痛就诊,接受了L2 - 3、L3 - 4和L4 - 5节段的穹顶式椎板成形术,术后无已知并发症。术后约4小时,他出现双侧下肢无力,以胫骨前肌和拇长伸肌(L4 - S1)最为明显,并伴有鞍区感觉缺失。MRI显示无急性压迫性改变。术后6个月进行了肌电图(EMG)检查,结果显示腓总神经和胫神经F波消失,波幅降低,符合潜在的轴索性神经病表现。他被转诊至神经科医生处寻求第二种意见,最终确诊为CIDP。随后开始静脉注射免疫球蛋白治疗,患者症状有所改善。本病例突出了结节病与CIDP之间的关联,并探讨了该疾病的病理生理学。对于结节病患者,腰椎手术后出现无力且MRI检查阴性的情况,应考虑CIDP的鉴别诊断。