Heffner R R, Barron S A, Jenis E H, Valeski J E
Arch Pathol Lab Med. 1979 Jun;103(6):310-3.
Thirty-two patients with adult-onset polymyositis uncomplicated by cancer or systemic connective tissue disease were studied. Muscle biopsy specimens were examined with direct immunofluorescence microscopy and results were compared with those in 94 control subjects. Sarcolemmal and sarcoplasmic staining were observed in both groups and considered to be nonspecific. Immune deposits in the muscle microvasculature were present in some cases of systemic lupus erythematosus and dermatomyositis but were not present in polymyositis. Our data suggest that the finding of vascular immunofluorescence excludes the diagnosis of adult polymyositis and implies that the pathogenesis of this disease and other idiopathic inflammatory myopathies may differ.
对32例无癌症或系统性结缔组织病并发的成人起病型多发性肌炎患者进行了研究。用直接免疫荧光显微镜检查肌肉活检标本,并将结果与94例对照受试者的结果进行比较。两组均观察到肌膜和肌浆染色,认为是非特异性的。系统性红斑狼疮和皮肌炎的某些病例中存在肌肉微血管中的免疫沉积物,但多发性肌炎中不存在。我们的数据表明,血管免疫荧光的发现排除了成人多发性肌炎的诊断,并意味着这种疾病和其他特发性炎性肌病的发病机制可能不同。