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对人类颞动脉进行光镜和电镜研究,特别关注与衰老、动脉粥样硬化和巨细胞动脉炎相关的改变。

Light and electron microscopic studies on human temporal arteries with special reference to alterations related to senescence, atherosclerosis and giant cell arteritis.

作者信息

Parker F, Healey L A, Wilske K R, Odland G F

出版信息

Am J Pathol. 1975 Apr;79(1):57-80.

PMID:164778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1913034/
Abstract

Temporal artery biopsy specimens from 26 patients of various ages with and without giant cell arteritis afforded an opportunity to examine several ultrastructural features of these human muscular arteries, including senescent and atherosclerotic alterations and the fine structural pathology of temporal arteritis. The unusual pathologic features of temporal arteritis were found superimposed on the progressive accumulation of smooth muscle cells, collagen and occasional discrete intimal atherosclerotic plaques in the intima of aging arteries. Two features of giant cell arteritis were conspicuous: first, the accumulation of large numbers of histiocytes and epitheloid and giant cells at the intimal-medial junction and second, fragmentation, degeneration and dissolution of the internal elastic lamina. The close proximity of the granulomatous reaction to the degenerating lamina suggests that these two aspects of the pathologic picture are in some way related, and possible immunologic mechanisms of this relationship are discussed on the basis of the ultrastructural findings.

摘要

对26名不同年龄段、患有或未患有巨细胞动脉炎的患者进行颞动脉活检,提供了一个机会来检查这些人体肌性动脉的几个超微结构特征,包括衰老和动脉粥样硬化改变以及颞动脉炎的精细结构病理学。发现颞动脉炎不同寻常的病理特征叠加在衰老动脉内膜中平滑肌细胞、胶原蛋白的逐渐积累以及偶尔出现的离散内膜动脉粥样硬化斑块上。巨细胞动脉炎有两个显著特征:第一,大量组织细胞、上皮样细胞和巨细胞在内膜 - 中膜交界处积聚;第二,内弹性膜的断裂、变性和溶解。肉芽肿反应与退变的内弹性膜紧密相邻,表明病理图像的这两个方面在某种程度上相关,并根据超微结构研究结果讨论了这种关系可能的免疫机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/abf774229a8a/amjpathol00461-0080-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/b03fd1a0cdc7/amjpathol00461-0081-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/c241917b1507/amjpathol00461-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/43e467d72346/amjpathol00461-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/c5cef212c3a2/amjpathol00461-0082-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/7a43dba3ef5c/amjpathol00461-0079-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/2f902d0d235d/amjpathol00461-0083-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/036bc04d5bff/amjpathol00461-0084-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/abf774229a8a/amjpathol00461-0080-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/b03fd1a0cdc7/amjpathol00461-0081-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/c241917b1507/amjpathol00461-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/43e467d72346/amjpathol00461-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/c5cef212c3a2/amjpathol00461-0082-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/7a43dba3ef5c/amjpathol00461-0079-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/2f902d0d235d/amjpathol00461-0083-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/036bc04d5bff/amjpathol00461-0084-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ef/1913034/abf774229a8a/amjpathol00461-0080-a.jpg

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