Suppr超能文献

病例报告。心内膜弹力纤维增生症导致胎儿心力衰竭。

Case report. Fetal cardiac failure resulting from endocardial fibroelastosis.

作者信息

Iwama M, Mori M, Kozaki T, Sato T

出版信息

Jpn Heart J. 1974 Nov;15(6):623-32. doi: 10.1536/ihj.15.623.

Abstract

An autopsy was performed on a female stillborn infant with generalized edema associated with ascites. On gross examination of the heart the pulmonary trunk was atretic from its origin of the heart to the bifurcation. The ductus arteriosus was abnormally wide. The right ventricle was hypoplastic and its endocardium was diffusely thickened. The inner surface of right ventricle appeared pale, obscuring the identification of trabeculae corneae and papillary muscles. At the posterior wall there was an extremely thin lesion where no apparnet cardiac muscle was contained. The tricuspid orifice was stenotic and the valve was hypoplactic. The right atrium was markedly enlarged and its wall was thickened. The foramen avale had patency of the valvular competent type. Atrial septal defect (ASD) was not present. The left ventricle was remarkably dilated with markedly thick wall. Ventricular septal defect (VSD) was present immediately beneath the right coronary cusp of the aortic valve. Light microscopic examination of the right ventricle revealed a marked increase of collagen and elastic fibers with extensive deposits of calcium not only in the endocardium but also in the deep portion of myocardium. Fibroelastosis appeared particularly prominent in the subendocardial layer. The muscle fibers surrounded by these penetrating fibers and deposits of calcium showed degeneration. The entire myocardial layer of the specific area in the right ventricle where the wall was paper-thin was fully replaced by fibers and calcium. Inflammatory cell infiltration was found only at some places of the pericardium. The left ventricular wall also showed fibroelastosis, although the degree of involvement was much less as compared to that seen in the right ventricle. There were no significant pathological changes in both atria.

摘要

对一名伴有腹水的全身水肿死产女婴进行了尸检。大体检查心脏时,肺动脉干自心脏起源至分叉处闭锁。动脉导管异常增宽。右心室发育不全,其内膜弥漫性增厚。右心室内表面苍白,难以辨认肉柱和乳头肌。后壁有一处极薄的病变,未见明显的心肌组织。三尖瓣口狭窄,瓣膜发育不全。右心房明显扩大,壁增厚。卵圆孔呈瓣膜功能正常型开放。不存在房间隔缺损(ASD)。左心室显著扩张,壁明显增厚。室间隔缺损(VSD)位于主动脉瓣右冠状动脉瓣叶下方紧邻处。右心室的光镜检查显示,不仅内膜,而且心肌深层的胶原纤维和弹性纤维显著增加,有广泛的钙沉积。纤维弹性组织增生在 subendocardial 层尤为突出。被这些穿透性纤维和钙沉积所包围的肌纤维出现变性。右心室壁薄如纸的特定区域的整个心肌层完全被纤维和钙替代。仅在心包的某些部位发现炎症细胞浸润。左心室壁也显示有纤维弹性组织增生,尽管受累程度与右心室相比要轻得多。两个心房均无明显病理变化。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验