Olivé M, Villanueva P, Ferrer I, Montero J, Martínez-Matos J A
Servicio de Neurología, Hospital de Bellvitge-Prínceps d'Espanya, Universidad de Barcelona.
Neurologia. 1994 May;9(5):202-3.
We report a 72-year-old woman with dysphagia as the only manifestation of inclusion body myositis (IBM). Although electrophysiological examination revealed subclinical abnormalities in limb muscles, dysphagia was the only symptom 4 years after the onset of the disease. Muscle biopsy showed rimmed vacuoles and cytoplasmic inclusions together with lymphocytic inflammation. IBM must be included in the differential diagnosis of isolated dysphagia.
我们报告了一名72岁女性,其吞咽困难是包涵体肌炎(IBM)的唯一表现。尽管电生理检查显示肢体肌肉存在亚临床异常,但吞咽困难是该疾病发病4年后唯一的症状。肌肉活检显示有镶边空泡、细胞质包涵体以及淋巴细胞炎症。孤立性吞咽困难的鉴别诊断必须考虑到IBM。