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颞动脉炎和/或风湿性多肌痛患者颞动脉的免疫学和组织学研究。

Immunological and histological studies of temporal arteries from patients with temporal arteritis and/or polymyalgia rheumatica.

作者信息

Waaler E, Tönder O, Milde E J

出版信息

Acta Pathol Microbiol Scand A. 1976 Jan;84(1):55-63. doi: 10.1111/j.1699-0463.1976.tb00110.x.

Abstract

Biopsies from the temporal arteries of 62 out of 80 patients presenting the clinical picture of temporal arteritis and/or polymyalgia rheumatica showed morphologically active or healed arteritis. Fifty-five of these biopsies revealed anti-IgG activity as measured by the mixed agglutination test. In 21 of the 27 cases which could be completely studied, the anti-IgG activity was connected with the presence of IgA, either alone, or together with IgG or IgM, or both, and complement. All of these 21 biopsies showed morphologically active granulomatous arteritis with signs of tissue destruction. In 6 biopsies, the active component appeared to be some type of Fc receptor in the tissue. Morphologically these biopsies showed either non-granulomatous mononuclear arteritis without definite necrosis or they represented various stages of healing arteritis with no or minor signs of tissue destruction. Weak anti-IgG activity was often found in a morphological type characterized by minimal inflammatory activity. These lesions are easily overlooked and the mixed agglutination test proved to be a good diagnostic tool in such cases. Arteries without anti-IgG activity showed no signs of active arteritis.

摘要

80例出现颞动脉炎和/或风湿性多肌痛临床表现的患者中,62例颞动脉活检显示有形态学上活动期或愈合期的动脉炎。通过混合凝集试验检测,其中55例活检显示有抗IgG活性。在27例可进行全面研究的病例中,21例的抗IgG活性与IgA的存在有关,IgA单独存在,或与IgG或IgM一起存在,或两者皆有,且伴有补体。所有这21例活检均显示有形态学上活动期的肉芽肿性动脉炎,并伴有组织破坏迹象。在6例活检中,活性成分似乎是组织中的某种类型的Fc受体。从形态学上看,这些活检显示为无明确坏死的非肉芽肿性单核细胞动脉炎,或者代表愈合期动脉炎的不同阶段,无组织破坏迹象或仅有轻微组织破坏迹象。在以炎症活动轻微为特征的形态学类型中,常发现弱抗IgG活性。这些病变很容易被忽视,而混合凝集试验在这类病例中被证明是一种很好的诊断工具。无抗IgG活性的动脉未显示活动期动脉炎迹象。

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