A Rare Case of Limited Muscle Involvement in Polyarteritis Nodosa

Sung Oh Song, R. Lee, M. Lim, S. Kwon, W. Park
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Abstract

Polyarteritis nodosa (PAN) is a systemic vasculitis that can affect multiple organs in its diffuse form and is associated with high rates of morbidity and mortality. From the standpoint of pathology, PAN is necrotizing arteritis predominantly involving medium and small muscular arteries, without glomerulonephritis or vasculitis in the arterioles, capillaries, or venules (1, 2). PAN has protean manifestations, and it may present as a systemic disease or in its limited form, be confined to a single organ (2). The limited form of PAN is rare and may pose a diagnostic challenge; it can mimic other common diseases, and its nonspecific presentation may lead to confusion or delays in diagnosis. Musculoskeletal system involvement in PAN is known to present as myalgia, arthralgia, polymyositis-like syndrome, asymmetric nondeforming polyarthritis, or rarely, as intermittent claudication, acute leg ischemia, or myopathy (2). Muscular involvement in PAN may occur as a component of systemic PAN or as a limited form. Patients with the limited form of PAN are known to present with pain, swelling, and tenderness of the lower leg (3). Magnetic resonance imaging (MRI) findings of muscular involvement in PAN have been reported in other studies, all in cases with the limited form of PAN (4). Most of the previous studies have reported nonspecific edematous signal changes in the affected muscles with hyper-signal intensities on T2-weighted or fat-saturated sequences (5), which may be found in all clinical mimics such as inflammatory or infectious myositis. Ultrasound is particularly useful in the diagnosis of largeand medium-sized vessel vasculitis, as the characteristic wall thickening of the affected arteries allows for the confirmation of a suspected diagnosis. However, only a few studies have reported ultrasonography findings for the limited form of PAN. Herein, we describe a rare case of PAN involving skeletal muscle as indicated on This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Received: January 16, 2021 Revised: February 22, 2021 Accepted: February 23, 2021
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结节性多动脉炎有限肌肉受累一例
结节性多动脉炎(PAN)是一种全身性血管炎,可以弥漫性形式影响多个器官,并与高发病率和死亡率有关。从病理学的角度来看,PAN是坏死性动脉炎,主要涉及中小肌动脉,在小动脉、毛细血管或小静脉中没有肾小球肾炎或血管炎(1,2)。PAN具有多种表现,可能表现为系统性疾病,也可能以有限的形式局限于单个器官(2)。PAN的有限形式是罕见的,可能会对诊断提出挑战;它可以模仿其他常见疾病,其非特异性表现可能导致诊断混乱或延误。众所周知,PAN中的肌肉骨骼系统受累表现为肌痛、关节痛、多发性肌炎样综合征、不对称非变性多关节炎,或很少表现为间歇性跛行、急性腿部缺血或肌病(2)。PAN的肌肉受累可能是全身PAN的一个组成部分,也可能是局限性的。已知局限性PAN患者会出现小腿疼痛、肿胀和压痛(3)。其他研究中也报道了PAN肌肉受累的磁共振成像(MRI)结果,所有这些都发生在PAN形式有限的病例中(4)。以前的大多数研究都报道了在T2加权或脂肪饱和序列上具有高信号强度的受累肌肉中的非特异性水肿信号变化(5),这可能在所有临床模拟物中发现,如炎症或感染性肌炎。超声在诊断大中型血管血管炎中特别有用,因为受影响动脉的特征性壁增厚可以确认可疑诊断。然而,只有少数研究报道了有限形式PAN的超声检查结果。在此,我们描述了一个罕见的涉及骨骼肌的PAN病例,如上所示。这是一篇根据知识共享归因非商业许可条款分发的开放获取文章(http://creativecommons.org/licenses/通过nc/4.0/),允许在任何媒体上进行不受限制的非商业使用、分发和复制,前提是正确引用了原作。接收日期:2021年1月16日修订日期:2021月22日接受日期:2021日2月23日
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