Allsop Vivianne L, Gaumnitz John, Xing Changhong, Goold Eric, Thomas Julie
Rheumatology, University of Utah Hospital, Salt Lake City, USA.
Internal Medicine, University of Utah Hospital, Salt Lake City, USA.
Cureus. 2025 May 7;17(5):e83683. doi: 10.7759/cureus.83683. eCollection 2025 May.
Myositis is a condition characterized by muscle inflammation due to multiple etiologies, including autoimmune disease, medication, and infection. Viral myositis is most frequently seen in children after influenza infection, but Parvovirus B19 has also rarely been associated with myositis. We report the case of a 42-year-old male with a medical history of low back pain due to spondylosis who presented to the hospital with a one-month history of bilateral thigh and calf pain associated with subjective weakness and a one-week history of fevers. His wife and son were diagnosed with Parvovirus B19 infection one month before his symptoms began. The physical exam was notable for prominent tenderness to palpation of the anterior thigh muscles and calves and mild swelling around the ankles without intra-articular effusion. Strength was normal in all extremities. Lower extremity MRI revealed extensive multifocal, patchy, and feathery edema throughout the lower extremities. Aldolase, C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and Parvovirus B19 serum IgM were elevated, but creatine kinase, extended myositis antibody panel, and 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase antibody were normal. A vastus lateralis muscle biopsy demonstrated mild acute myopathic changes with patchy upregulation of major histocompatibility complex (MHC) class I antigens. Parvovirus B19 polymerase chain reaction (PCR) on the muscle tissue was positive. The patient was diagnosed with myositis due to Parvovirus B19 infection and started on scheduled naproxen. Five months later, his symptoms had completely resolved, and he no longer required naproxen. A literature review of PubMed, Ovid, Scopus, Web of Science, and Cochrane databases for English-language articles using the search terms "idiopathic inflammatory myopathy" OR "myositis" OR "inflammatory myopathy" OR "dermatomyositis" OR "polymyositis" AND "Parvovirus B19" OR "parvovirus" revealed six other cases of myositis associated with Parvovirus B19 infections, although two of the six cases had characteristics of dermatomyositis rather than viral myositis. Aside from the patient with dermatomyositis, one other patient had a muscle biopsy with positive Parvovirus B19 testing. To our knowledge, our case is the second description of biopsy-proven Parvovirus B19 myositis, and the first to describe specific histopathology. Further, ours is the first case of biopsy-proven Parvovirus B19 myositis to be successfully treated with non-steroidal anti-inflammatory drugs (NSAIDs) in an adult.
肌炎是一种由于多种病因引起的肌肉炎症性疾病,这些病因包括自身免疫性疾病、药物和感染。病毒性肌炎在儿童流感感染后最为常见,但细小病毒B19也很少与肌炎相关。我们报告了一例42岁男性病例,他有因脊柱病导致的腰痛病史,因双侧大腿和小腿疼痛伴主观无力1个月及发热1周入院。在他症状出现前1个月,他的妻子和儿子被诊断为细小病毒B19感染。体格检查发现大腿前部肌肉和小腿触诊时有明显压痛,踝关节周围轻度肿胀但无关节内积液。所有肢体肌力正常。下肢MRI显示整个下肢广泛的多灶性、斑片状和羽毛状水肿。醛缩酶、C反应蛋白(CRP)、红细胞沉降率(ESR)和细小病毒B19血清IgM升高,但肌酸激酶、扩展的肌炎抗体谱和3-羟基-3-甲基戊二酰辅酶A(HMG CoA)还原酶抗体正常。股外侧肌活检显示轻度急性肌病改变,主要组织相容性复合体(MHC)I类抗原呈斑片状上调。肌肉组织的细小病毒B19聚合酶链反应(PCR)呈阳性。该患者被诊断为细小病毒B19感染所致肌炎,并开始按计划服用萘普生。5个月后,他的症状完全缓解,不再需要萘普生。对PubMed、Ovid、Scopus、Web of Science和Cochrane数据库进行文献检索,以查找使用搜索词“特发性炎性肌病”或“肌炎”或“炎性肌病”或“皮肌炎”或“多发性肌炎”以及“细小病毒B19”或“细小病毒”的英文文章,结果发现另外6例与细小病毒B19感染相关的肌炎病例,尽管这6例中有2例具有皮肌炎而非病毒性肌炎的特征。除了皮肌炎患者外,另一名患者的肌肉活检细小病毒B19检测呈阳性。据我们所知,我们的病例是第二例经活检证实的细小病毒B19肌炎描述,也是第一例描述特定组织病理学的病例。此外,我们的病例是第一例经活检证实的细小病毒B19肌炎在成人中用非甾体抗炎药(NSAIDs)成功治疗的病例。