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Inclusion body myositis: morphological clues to correct diagnosis.

机译:包涵体肌炎:正确诊断的形态学线索。

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摘要

The aim of this study was to investigate variability of morphological changes found in patients with sporadic inclusion body myositis, to assess the diagnostic value of muscle biopsy. The study included all 43 definite inclusion body myositis patients (86 biopsies) diagnosed at Sahlgrenska University Hospital, Gothenburg, Sweden, between 1984 and 2000. Invasion of mononuclear inflammatory cells in non-necrotic muscle fibres was found in 72 of 86 specimens, while all investigated biopsies showed up-regulation of major histocompatibility complex class I. Cytochrome c oxidase-negative muscle fibres were demonstrated in 84 of 86 biopsies. Rimmed vacuoles were present in all specimens from the vastus lateralis and tibialis muscles, and in 43 of 51 biopsies from the deltoid muscle. In cases with clinical suspicion of inclusion body myositis, where the muscle biopsy does not show inflammatory cell infiltration and rimmed vacuoles, inclusion body myositis should still be considered if there are cytochrome c oxidase-negative fibres and up-regulation of major histocompatibility complex class I. In such cases repeat muscle biopsy may be helpful.
机译:这项研究的目的是调查散发性包涵体肌炎患者中发现的形态学变化的变异性,以评估肌肉活检的诊断价值。这项研究包括1984年至2000年之间在瑞典哥德堡的萨格伦斯卡大学医院确诊的所有43例明确包涵体肌炎患者(86例活检)。在86例标本中有72例发现非坏死性肌纤维中有单核炎性细胞浸润。研究的活组织检查显示主要组织相容性复合体I类上调。在86例活组织检查中,有84个细胞色素c氧化酶阴性肌肉纤维被证实。在股外侧肌和胫骨肌肉的所有标本中,以及在三角肌的51份活检中,有43个存在标本的液泡。在临床怀疑包涵体肌炎的病例中,如果肌肉活检未显示炎性细胞浸润和空泡边缘,如果细胞色素c氧化酶阴性纤维和主要组织相容性复合体I类上调,则仍应考虑包涵体肌炎在这种情况下,重复肌肉活检可能会有所帮助。

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