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平山病的临床、电诊断、超声及放射学表现:两例报告并文献复习

Clinical, Electrodiagnostic, Sonographic, and Radiological Findings of Hirayama Disease: A Report of Two Cases and a Review of the Literature.

作者信息

Shields Lisa B, Iyer Vasudeva G, Zhang Yi Ping, Shields Christopher B

机构信息

Norton Neuroscience Institute, Norton Healthcare, Louisville, USA.

Clinical Neurophysiology, Neurodiagnostic Center of Louisville, Louisville, USA.

出版信息

Cureus. 2024 Nov 18;16(11):e73914. doi: 10.7759/cureus.73914. eCollection 2024 Nov.

Abstract

Hirayama disease (HD) is a rare disorder characterized by insidious asymmetric neurogenic atrophy primarily involving the upper extremities. HD most commonly affects adolescent males and has a favorable prognosis for arrest of progression. Electrodiagnostic (EDX) studies show chronic denervation changes in the distal upper extremity muscles. A cervical spine MRI in neck flexion may reveal compression of the cervical ventral spinal cord. We report clinical, EDX, and MRI findings in two cases of HD. The first case involved a 15-year-old male with a six-month history of progressive weakness, wasting, and tremulous movements of the left hand without pain or paresthesia. A physical exam revealed marked wasting of the left intrinsic hand muscles with polyminimyoclonus. Needle electromyography (EMG) revealed fasciculations (simultaneous with the polyminimyoclonus) while at rest and recruitment of 1-2 large polyphasic units in the left C8, T1, and, to a lesser extent, the C7 distribution. A T2-weighted flexion cervical spine MRI revealed narrowing and anterior displacement of the posterior dura of the cervical cord, leading to cord compression at C5-6 and C6-7. At last contact 11 years following symptom initiation, the patient continued to complain of profound weakness of the left hand without pain or numbness. The second case involved a 17-year-old male who was found to have wasting of the intrinsic muscles of the non-dominant left hand on a routine physical examination. The left first dorsal interosseus, abductor digiti minimi, abductor pollicis brevis, and extensor pollicis longus muscles were found to be clinically weak. Polyminimyoclonus involving all fingers of the left hand was also observed. A needle EMG demonstrated fasciculations with large amplitudes and wide duration motor unit potentials in the left C8, T1, and, to a lesser extent, C7 distribution. An ultrasound study showed frequent fasciculations in the left intrinsic hand muscles and the distal forearm muscles simultaneously with the polyminimyoclonus. A T2-weighted cervical spine MRI scan in the flexed sagittal position revealed anterior displacement of the dura and an enlarged epidural space from C4-C7. At last follow-up 11 months later, the findings were unchanged. The EDX studies and cervical MRI findings were consistent with HD in both cases. The role of EDX studies and cervical spine flexion MRI in diagnosing HD and the correlation between polyminimyoclonus and fasciculations are highlighted.

摘要

平山病(HD)是一种罕见的疾病,其特征为隐匿性不对称神经源性萎缩,主要累及上肢。HD最常影响青少年男性,病情进展停止后预后良好。电诊断(EDX)研究显示上肢远端肌肉存在慢性失神经改变。颈部屈曲位的颈椎MRI可能显示颈段腹侧脊髓受压。我们报告了两例HD患者的临床、EDX及MRI检查结果。第一例为一名15岁男性,有6个月的左手进行性无力、萎缩及震颤病史,无疼痛或感觉异常。体格检查发现左手固有肌明显萎缩并伴有多灶性肌阵挛。针极肌电图(EMG)显示静息时存在肌束震颤(与多灶性肌阵挛同时出现),在左侧C8、T1以及程度较轻的C7分布区募集到1 - 2个大的多相运动单位。T2加权颈部屈曲位颈椎MRI显示颈髓后硬膜变窄并向前移位,导致C5 - 6和C6 - 7水平脊髓受压。在症状出现11年后的最后一次随访中,患者仍诉说左手严重无力,无疼痛或麻木感。第二例为一名17岁男性,在常规体格检查中发现非优势侧左手固有肌萎缩。发现左侧第一背侧骨间肌、小指展肌、拇短展肌及拇长伸肌在临床上肌力减弱。还观察到累及左手所有手指的多灶性肌阵挛。针极EMG显示在左侧C8、T1以及程度较轻的C7分布区存在高波幅、宽时限的运动单位电位伴肌束震颤。超声检查显示左手固有肌和前臂远端肌肉频繁出现肌束震颤,与多灶性肌阵挛同时发生。矢状面屈曲位T2加权颈椎MRI扫描显示硬膜向前移位,C4 - C7硬膜外间隙增宽。在11个月后的最后一次随访中,检查结果无变化。两例患者的EDX检查及颈椎MRI表现均符合HD。强调了EDX检查和颈椎屈曲位MRI在HD诊断中的作用以及多灶性肌阵挛与肌束震颤之间的相关性。

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