Subash Meera, Patel Gaurav, Welker John, Nugent Kenneth
Texas Tech University Health Sciences Center, Lubbock, TX, USA.
J Investig Med High Impact Case Rep. 2014 May 9;2(2):2324709614535203. doi: 10.1177/2324709614535203. eCollection 2014 Apr-Jun.
Background. Brachial neuritis (BN) is a rare inflammatory condition of peripheral nerves, usually involving the cervicobrachial plexus. These patients present with sudden onset of shoulder and arm pain that evolves into muscle weakness and atrophy.. Case Report. A 33-year-old woman presented with a 1-month history of diffuse pain in her thorax. She had no trauma or inciting incident prior to the onset of this pain and was initially treated for muscle spasms. The patient was seen in the emergency room multiple times and was treated with several courses of antibiotics for pneumonia on the basis of clinical symptoms and abnormal x-rays. The pleuritic chest pain persisted for at least 4 months, and the patient was eventually admitted for worsening pain and dyspnea. On physical examination, crackles were heard at both lung bases, and chest inspection revealed increased expansion in the upper thorax but poor expansion of the lower thorax and mild paradoxical respiration. "Sniff" test revealed no motion of the left hemidiaphragm and reduced motion on the right hemidiaphragm. Her computed tomography scan revealed bilateral atelectasis, more severe at the left base. She reported no symptoms involving her joints or skin or abdomen. Her presentation and clinical course are best explained by BN with a bilateral diaphragmatic weakness. However, she had a positive ANA, RF, anti-RNP antibody, and anti SS-A. Conclusion. Patients with BN can present with diffuse thoracic pain, pleuritic chest pain, and diaphragmatic weakness. Our patient may represent a case of connective tissue disease presenting with brachial plexus neuritis.
背景。臂丛神经炎(BN)是一种罕见的周围神经炎症性疾病,通常累及颈臂丛神经。这些患者表现为肩部和手臂突然疼痛,随后发展为肌肉无力和萎缩。病例报告。一名33岁女性,有1个月的胸部弥漫性疼痛病史。在疼痛发作前她没有外伤或诱发事件,最初被诊断为肌肉痉挛并接受治疗。该患者多次前往急诊室就诊,根据临床症状和异常的X线检查结果,接受了多个疗程的抗生素治疗以治疗肺炎。胸膜炎性胸痛持续了至少4个月,最终患者因疼痛加剧和呼吸困难入院。体格检查发现双肺底部可闻及湿啰音,胸部视诊显示上胸部扩张增加,但下胸部扩张不良且有轻度矛盾呼吸。“嗅气”试验显示左侧半膈肌无运动,右侧半膈肌运动减弱。她的计算机断层扫描显示双侧肺不张,左侧底部更为严重。她没有报告涉及关节、皮肤或腹部的症状。她的表现和临床病程最可能的解释是臂丛神经炎合并双侧膈肌无力。然而,她的抗核抗体、类风湿因子、抗核糖核蛋白抗体和抗SS - A均呈阳性。结论。臂丛神经炎患者可能表现为弥漫性胸痛、胸膜炎性胸痛和膈肌无力。我们的患者可能是一例以臂丛神经炎为表现的结缔组织病。