Suppr超能文献

见于冯雷克林霍增氏病神经纤维瘤性损害中的产生黑色素的细胞——荧光法(法尔克和希拉尔普)研究

Melanin-producing cells seen in neurofibromatous lesions of Recklinghausen's disease -- a study with fluorescence method (Falck and Hillarp).

作者信息

Morishima T, Ishikawa T, Endo M

出版信息

Arch Dermatol Res (1975). 1976 Oct 27;256(3):213-21. doi: 10.1007/BF00572486.

Abstract

A case diagnosed to have the lesion of pachydermatocele type of Recklinghausen's disease in a 28-year-old female was studied mainly by means of fluorescence method (Falck and Hillarp). Histopathological examination revealed that the lesion was composed of Ota's nevus-like changes in the epidermis to the middermis and of proliferation of neurofibromatous tissues coexisting with melanin-producing cells in the lower dermis to the subcutaneous adipose tissue. Melanin-producing cells in the neurofibromatous lesion were shown by fluorescence method to have characteristics of nevus cells rather than of melanocytes. Innervation of monoaminergic and cholinergic nerves was not found to the arteries in neurofibromas. These findings are thought to suggest that the abnormalities of not only Schwannian cells and melanocytes of neural crest origin but also of nevus cells and autonomous nerves of neural crest origin are related with the pathogenesis of pachydermatocele type of Recklinghausen's disease.

摘要

对一名28岁女性诊断为厚皮性神经纤维瘤病型雷克林霍增氏病病变的病例主要采用荧光法(法尔克和希拉尔普)进行研究。组织病理学检查显示,病变由表皮至中真皮的太田痣样改变以及真皮下部至皮下脂肪组织中与产生黑色素细胞共存的神经纤维瘤组织增生构成。通过荧光法显示,神经纤维瘤病变中的产生黑色素细胞具有痣细胞而非黑素细胞的特征。未发现神经纤维瘤内动脉有单胺能和胆碱能神经支配。这些发现被认为提示,不仅神经嵴起源的施万细胞和黑素细胞异常,而且神经嵴起源的痣细胞和自主神经异常均与厚皮性神经纤维瘤病型雷克林霍增氏病的发病机制有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验