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一例肱动脉黏液样变性的超微结构改变

Ultrastructural changes in a case of mucoid degeneration of the brachial artery.

作者信息

Renno W M, Wali M A

机构信息

Department of Anatomy, College of Medicine, King Saud University, Abha, Saudi Arabia.

出版信息

Pathology. 1999 May;31(2):152-7. doi: 10.1080/003130299105359.

Abstract

An electron microscopic (EM) description of mucoid degeneration of the brachial artery in a 67 year old man is presented. In this case, the affected artery showed mucoid degeneration of the intima and media circumferentially, dissecting and destroying the muscle fibres. Ultrastructurally, mucoid degenerating muscle cells showed numerous large mucin-containing vesicles in the cytoplasm. Cells were widely separated by large accumulation of mucoid material, which appeared to penetrate the extracellular collagen fibre bundles. Most of the nuclei of the smooth muscle cells displayed typical necrotic changes undergoing dissolution or having already broken up into discrete fragments. This case of intimo-medial degeneration (IMMD) suggests that the condition could arise spontaneously anywhere in the inner coats of the arterial system away from the vessels that are close to synovial joints. This is a rare presentation of IMMD of arteries, which has been described mainly in the aorta and its major branches.

摘要

本文呈现了一位67岁男性肱动脉黏液样变性的电子显微镜(EM)描述。在该病例中,受累动脉内膜和中膜呈环形黏液样变性,分离并破坏肌纤维。超微结构上,黏液样变性的肌细胞胞质内可见大量含黏蛋白的囊泡。细胞被大量黏液样物质广泛分隔,这些黏液样物质似乎穿透了细胞外胶原纤维束。大多数平滑肌细胞核呈现典型的坏死改变,正在溶解或已破碎成离散的碎片。这种内膜-中膜变性(IMMD)病例表明,该病症可能在动脉系统内皮层远离靠近滑膜关节的血管的任何部位自发出现。这是动脉IMMD的一种罕见表现,主要在主动脉及其主要分支中有所描述。

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