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多发性肌炎和皮肌炎的肌肉活检:一项临床病理研究。

Muscle biopsy in polymyositis and dermatomyositis: a clinicopathological study.

作者信息

Schwarz H A, Slavin G, Ward P, Ansell B M

出版信息

Ann Rheum Dis. 1980 Oct;39(5):500-7. doi: 10.1136/ard.39.5.500.

Abstract

The initial muscle biopsies of 30 patients with active polymyositis or dermatomyositis have been assessed histologically and morphometrically. Only 1 patient (3.3%) had a normal biopsy, while 3 had a normal electromyograph and 8 had a normal serum CPK level. No significant morphological differences were found between the various diagnostic subgroups. Sequential biopsies of 11 of these patients treated either with corticosteroids only or with intensive immunosuppression were studied. With response to treatment atrophy factors, variability coefficients, internal nuclei count, and the various histological changes improved in the whole group of patients. However, there was no consistent correlation between any of the morphological features or between these and clinical parameters in individual patients. The percentage of fibres with internal nuclei in the initial biopsy was lower (P < 0.001) in patients responding to up to 60 mg prednisolone per day than in those who eventually required cytotoxic drugs in addition.

摘要

对30例活动性多发性肌炎或皮肌炎患者的初始肌肉活检进行了组织学和形态学评估。只有1例患者(3.3%)活检结果正常,3例肌电图正常,8例血清肌酸磷酸激酶(CPK)水平正常。在不同诊断亚组之间未发现明显的形态学差异。对其中11例仅接受皮质类固醇治疗或强化免疫抑制治疗的患者进行了连续活检研究。随着对治疗的反应,全组患者的萎缩因子、变异系数、内核计数以及各种组织学变化均有所改善。然而,在个体患者中,任何形态学特征之间或这些特征与临床参数之间均无一致的相关性。与最终还需要细胞毒性药物的患者相比,每天接受最多60毫克泼尼松龙治疗且有反应的患者,其初始活检中含内核纤维的百分比更低(P<0.001)。

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