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海绵状血管畸形的病理学

Pathology of cavernous malformations.

作者信息

Cox Efrem M, Bambakidis Nicholas C, Cohen Mark L

机构信息

Department of Neurosurgery, University Hospitals, Case Western Reserve University, Cleveland, OH, USA.

Department of Neurosurgery, University Hospitals, Case Western Reserve University, Cleveland, OH, USA.

出版信息

Handb Clin Neurol. 2017;143:267-277. doi: 10.1016/B978-0-444-63640-9.00025-4.

Abstract

Cavernous malformations (CMs) are low-pressure angiographically occult lesions, composed of blood-filled sinusoidal locules known as "caverns." Although these lesions were once believed to be congenital in nature, there is compelling evidence to support de novo formation of CMs as well. They can occur as sporadic lesions or be inherited in an autosomal-dominant phenotype in familial forms of the disease. The pathophysiology of CMs is commonly believed to be due to abnormal vascular pathology. Three genes, CCM1, CCM2, and CCM3, have been extensively studied for their role in vascular pathology, resulting in abnormal angiogenesis and compromising the structural integrity of vessel endothelial cell. The expression of growth factors has been researched to gain insight into the dynamic behavior of CM lesions. Gross and microscopic images are utilized in this chapter to illustrate the pathologic findings of these lesions. Ultrastructural analysis demonstrates the aberrations in CM endothelial cells and structural integrity that may provide better understanding into how and why these lesions have a propensity to hemorrhage.

摘要

海绵状血管畸形(CMs)是血管造影隐匿性的低压病变,由充满血液的窦状腔隙即“海绵体”组成。尽管这些病变曾被认为本质上是先天性的,但也有令人信服的证据支持CMs的新生形成。它们可表现为散发性病变,或以常染色体显性表型遗传,呈家族性疾病形式。CMs的病理生理学通常被认为是由于异常的血管病变。CCM1、CCM2和CCM3这三个基因在血管病变中的作用已得到广泛研究,导致血管生成异常并损害血管内皮细胞的结构完整性。对生长因子的表达进行了研究,以深入了解CM病变的动态行为。本章利用大体和微观图像来说明这些病变的病理发现。超微结构分析显示了CM内皮细胞的异常和结构完整性,这可能有助于更好地理解这些病变如何以及为何容易出血。

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