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早期丛状肺血管病的超微结构

Ultrastructure of early plexogenic pulmonary arteriopathy.

作者信息

Heath D, Smith P, Gosney J

机构信息

Department of Pathology, University of Liverpool, UK.

出版信息

Histopathology. 1988 Jan;12(1):41-52. doi: 10.1111/j.1365-2559.1988.tb01915.x.

Abstract

A lung biopsy specimen from a young woman with the clinical features of primary pulmonary hypertension showed grade 2 plexogenic pulmonary arteriopathy. Electron microscopy revealed 'dark', electron-dense smooth muscle cells in the inner part of the media of muscular pulmonary arteries. Many of these transformed myocytes had migrated into the lumens of pulmonary arteries and arterioles which they occluded. This migration of smooth muscle cells was associated with a substantial increase in the number of pulmonary endocrine cells in the bronchioles containing bombesin and calcitonin.

摘要

一名具有原发性肺动脉高压临床特征的年轻女性的肺活检标本显示为2级丛状肺动脉病。电子显微镜检查发现,在肌性肺动脉中膜内侧有“深色”、电子密度高的平滑肌细胞。许多这些转化的肌细胞迁移到肺动脉和小动脉管腔中并造成阻塞。平滑肌细胞的这种迁移与含有蛙皮素和降钙素的细支气管中肺内分泌细胞数量的大量增加有关。

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