Suppr超能文献

伴有神经内脏贮积的晚期尼曼-匹克病:一个分类问题。

Late Niemann-Pick disease with neurovisceral storage: a classification problem.

作者信息

McFarlane J, Murray L, Bradbury K, Cowen P N

机构信息

Department of Pathology, University of Leeds.

出版信息

J Clin Pathol. 1988 Jun;41(6):619-22. doi: 10.1136/jcp.41.6.619.

Abstract

A 51 year old man presented in 1969 with slowly progressive cerebellar ataxia of unknown origin. He was admitted to hospital aged 68 after a fall, and a ruptured spleen was removed at laparotomy. Histological analysis of the spleen suggested Niemann-Pick disease, which was subsequently confirmed. He deteriorated and died of bronchopneumonia shortly afterwards: subdural haemorrhage with storage material in neurones was found at necropsy. This late onset case of Niemann-Pick disease with neurovisceral storage is unusual and may represent a variant.

摘要

一名51岁男性于1969年出现病因不明的缓慢进展性小脑共济失调。他68岁时因跌倒入院,剖腹探查时切除了破裂的脾脏。脾脏组织学分析提示尼曼-匹克病,随后得到证实。此后不久他病情恶化,死于支气管肺炎:尸检发现硬膜下出血,神经元中有储存物质。这种伴有神经内脏储存的迟发性尼曼-匹克病病例不常见,可能代表一种变异型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af7d/1141541/9dc86d599bd9/jclinpath00338-0020-a.jpg

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