Medicine, Medical College of Wisconsin, Wauwatosa, Wisconsin, USA
Rheumatology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
BMJ Case Rep. 2021 Feb 19;14(2):e237647. doi: 10.1136/bcr-2020-237647.
Necrotising myopathy is an autoimmune disease that commonly affects muscles. Here we examine a case of a middle-aged women presenting with a chief report of shortness of breath, who subsequently developed muscle weakness. Her clinical course was complicated by respiratory failure and pulmonary hypertension likely due to the underlying pathology of signal recognition particle-positive necrotising myopathy. After further evaluation, her shortness of breath was thought to be secondary to muscle pathology rather than cardiopulmonary pathology. She was transferred to our institution for workup by rheumatology. At the time of admission, 6 months after initial presentation, her weakness progressed, so that she was unable to lift her arms and legs against gravity. Furthermore, neurological examination revealed mild facial and nuchal weakness, severe proximal weakness, more moderate distal weakness and global areflexia.
坏死性肌病是一种常见的影响肌肉的自身免疫性疾病。在这里,我们检查了一名中年妇女的病例,她主要报告呼吸急促,随后出现肌肉无力。她的临床病程因信号识别颗粒阳性坏死性肌病的潜在病理学而复杂化,可能导致呼吸衰竭和肺动脉高压。进一步评估后,她的呼吸急促被认为是肌肉病理学而不是心肺病理学的继发性疾病。她因接受风湿病学检查而被转至我们的机构。入院时,即初次就诊后 6 个月,她的无力症状加重,以至于她无法对抗重力抬起手臂和腿部。此外,神经系统检查显示轻度面部和颈项无力、严重的近端无力、中度远端无力和全身反射消失。