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肌型结节性多动脉炎。

Muscular polyarteritis nodosa.

机构信息

Department of Physical Medicine and Rehabilitation, College of Medicine, Korea University, Ansan City, Korea.

出版信息

J Clin Rheumatol. 2012 Aug;18(5):249-52. doi: 10.1097/RHU.0b013e318262e3dd.

Abstract

We present an unusual case of a 26-year-old man with muscular polyarteritis nodosa (PAN) with severe calf pain and gait disturbance. Magnetic resonance imaging of the lower limbs demonstrated highly increased signal intensity in both soleus muscles and the lateral head of the left gastrocnemius muscle. Biopsies of the soleus muscle showed acute necrotizing arteritis. The calf pain and limited range of motion of ankle dorsiflexion subsided from day 1 on administration of oral corticosteroid at high dosage and were completely resolved by 4 months. After tapering corticosteroid to 10 mg, symptoms recurred. A combined regimen of immunosuppressants was found to maintain symptomatic relief.Muscular PAN should be included in the differential diagnosis of a patient presenting with symptoms of acute or subacute calf pain. Although this muscular PAN was so far been benign, complete remission of the underlying process may be difficult to achieve.

摘要

我们报告一例 26 岁男性肌型结节性多动脉炎(PAN)病例,表现为严重小腿疼痛和步态障碍。下肢磁共振成像显示双侧比目鱼肌和左侧腓肠肌外侧头信号高度增高。比目鱼肌活检显示急性坏死性动脉炎。大剂量口服皮质类固醇治疗后第 1 天小腿疼痛和踝关节背屈活动范围受限即缓解,4 个月完全缓解。皮质类固醇逐渐减量至 10mg 时症状再次出现。联合免疫抑制剂治疗可维持症状缓解。出现急性或亚急性小腿疼痛的患者应考虑肌型 PAN 作为鉴别诊断。虽然该例肌型 PAN 目前为良性,但基础病变的完全缓解可能难以实现。

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