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The Natural History of Uterine Leiomyomas: Light and Electron Microscopic Studies of Fibroid Phases Interstitial Ischemia Inanosis and Reclamation

机译:子宫平滑肌瘤的自然历史:肌瘤期间质性缺血贫血和围垦的光和电子显微镜研究

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摘要

We propose, and offer evidence to support, the concept that many uterine leiomyomas pursue a self-limited life cycle. This cycle can be arbitrarily divided on the basis of morphologic assessment of the collagen content into 4 phases: (1) proliferation, (2) proliferation and synthesis of collagen, (3) proliferation, synthesis of collagen, and early senescence, and (4) involution. Involution occurs as a result of both vascular and interstitial ischemia. Interstitial ischemia is the consequence of the excessive elaboration of collagen, resulting in reduced microvascular density, increased distance between myocytes and capillaries, nutritional deprivation, and myocyte atrophy. The end stage of this process is an involuted tumor with a predominance of collagen, little to no proliferative activity, myocyte atrophy, and myocyte cell death. Since many of the dying cells exhibit light microscopic and ultrastructural features that appear distinct from either necrosis or apoptosis, we refer to this process as inanosis, because it appears that nutritional deprivation, or inanition, is the underlying cause of cell death. The disposal of myocytes dying by inanosis also differs in that there is no phagocytic reaction, but rather an apparent dissolution of the cell, which might be viewed as a process of reclamation as the molecular contents are reclaimed and recycled.
机译:我们提出并提供证据支持许多子宫平滑肌瘤追求自我限制的生命周期的概念。可以根据胶原蛋白含量的形态学评估将该循环任意分为四个阶段:(1)增殖,(2)胶原蛋白的增殖和合成,(3)增殖,胶原蛋白的合成和早期衰老,和(4 )内卷。发生内翻是血管和间质缺血的结果。间质性缺血是胶原蛋白过度加工的结果,导致微血管密度降低,心肌细胞与毛细血管之间的距离增加,营养缺乏和心肌细胞萎缩。该过程的最后阶段是一个以胶原蛋白为主,几乎没有或没有增殖活性,肌细胞萎缩和肌细胞死亡的肿瘤。由于许多垂死的细胞显示出与坏死或凋亡不同的光学显微和超微结构特征,因此我们将此过程称为贫血,因为营养缺乏或贫血似乎是细胞死亡的根本原因。因贫血而死亡的心肌细胞的处置方式也有所不同,因为没有吞噬反应,而是细胞的明显溶解,这可以看作是回收过程,因为分子内容物被回收和再循环。

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