Hakobyan Knkush, Acob Talar, Aleksanyan Mesrop, Jumaah Omar, Prabhakaran Sajina
Internal Medicine Residency Program, Capital Health Regional Medical Center, Trenton, USA.
Oncology, Yerevan State Medical University, Yerevan, ARM.
Cureus. 2024 Jun 11;16(6):e62153. doi: 10.7759/cureus.62153. eCollection 2024 Jun.
Myositis is a group of rare autoimmune disorders characterized by chronic inflammation of skeletal muscles that leads to a hallmark triad of muscle weakness, fatigue, and myalgia. Extra-muscular manifestations are sometimes seen and involve various organ systems, including the gastrointestinal (GI) tract. In this case series, two patients with polymyositis (PM) and dermatomyositis (DM), both of whom developed dysphagia as a complication of myositis, are discussed. Case 1 was a female with a known history of biopsy-proven dermatomyositis who presented with progressive peripheral edema and weakness affecting all extremities. Concurrently, she displayed symptoms of pneumonia and dysphagia associated with frequent spontaneous or self-induced vomiting to alleviate retrosternal discomfort. Esophagogastroduodenoscopy (EGD) revealed esophageal dilatation and an absence of a contractile response, consistent with myositis. Treatment comprised intravenous immunoglobulin (IVIG), mycophenolate, and lifestyle modifications, including dietary adjustments and maintaining an upright position postprandial. The second case was a female with muscle weakness and dysphagia. Video-fluoroscopic swallow assessment was significant for pharyngeal dysfunction without a sensory response to penetrated material, and the patient was at high risk of aspiration with any oral intake. The presence of pharyngeal dysfunction and dysphagia prompted treatment with IVIG, mycophenolate, and percutaneous endoscopic gastrostomy (PEG) tube placement. These cases have highlighted the upper GI complications observed in patients with myositis, accentuating the necessity for a personalized treatment approach. Timely intervention has shown promising results in symptomatic relief and improving patient outcomes. This emphasizes the importance of a multidisciplinary approach when addressing myositis-related upper GI manifestations.
肌炎是一组罕见的自身免疫性疾病,其特征是骨骼肌的慢性炎症,导致肌肉无力、疲劳和肌痛这一典型三联征。有时会出现肌肉外表现,累及包括胃肠道(GI)在内的各种器官系统。在本病例系列中,讨论了两名患有多发性肌炎(PM)和皮肌炎(DM)的患者,他们均因肌炎并发症出现吞咽困难。病例1是一名女性,有活检证实的皮肌炎病史,表现为进行性外周水肿和累及所有肢体的无力。同时,她出现肺炎症状以及吞咽困难,伴有频繁的自发或自我诱发呕吐以缓解胸骨后不适。食管胃十二指肠镜检查(EGD)显示食管扩张且无收缩反应,符合肌炎表现。治疗包括静脉注射免疫球蛋白(IVIG)、霉酚酸酯以及生活方式调整,包括饮食调整和餐后保持直立姿势。第二个病例是一名有肌肉无力和吞咽困难的女性。视频荧光吞咽评估显示存在咽部功能障碍,对穿透物质无感觉反应,患者经口摄入任何食物均有高误吸风险。咽部功能障碍和吞咽困难的存在促使采用IVIG、霉酚酸酯治疗以及经皮内镜下胃造口术(PEG)置管。这些病例突出了肌炎患者中观察到的上消化道并发症,强调了个性化治疗方法的必要性。及时干预在缓解症状和改善患者预后方面已显示出有希望的结果。这强调了在处理与肌炎相关的上消化道表现时采用多学科方法的重要性。