Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China.
Department of Pathology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China.
Australas J Dermatol. 2019 Aug;60(3):e227-e231. doi: 10.1111/ajd.12973. Epub 2018 Dec 27.
Eosinophilic fasciitis is a rare scleroderma-like syndrome with an unknown aetiology. The characteristics of this disorder include lymphoplasmacytic inflammation involving the subcutaneous fat septa and fascia. Eosinophilic myositis is diagnosed when inflammation extends into the muscles. Here, we describe four patients who developed eosinophilic fasciitis, three of whom developed eosinophilic fasciitis with myositis. Fascial and muscle biopsies were used to confirm the diagnoses. All the patients presented with musculoskeletal symptoms; their electromyographic examinations showed myogenic lesions [short-duration, low-amplitude and polyphasic motor unit action potentials (MUPs), so-called myopathic changes, frequently with abnormal spontaneous activity], in contrast with findings from other reports.
嗜酸性筋膜炎是一种罕见的类硬皮病综合征,病因不明。该病的特征为淋巴浆细胞浸润累及皮下脂肪间隔和筋膜。当炎症延伸至肌肉时,则诊断为嗜酸性肌炎。在此,我们描述了 4 例发生嗜酸性筋膜炎的患者,其中 3 例发生伴肌炎的嗜酸性筋膜炎。筋膜和肌肉活检用于确诊。所有患者均表现为肌肉骨骼症状;他们的肌电图检查显示肌源性病变(短时限、低幅度和多相运动单位动作电位[MUP],即所谓的肌病改变,常伴有异常自发性活动),与其他报道的结果不同。