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伴有脑脊液异常的罕见家族性共济失调患者直肠活检标本的超微结构

Ultrastructure of rectal biopsy specimens in unusual familial ataxia with cerebrospinal fluid abnormality.

作者信息

Nakamura I, Fukutani Y, Kobayashi K, Kawasaki Y, Sakamoto H, Yamaguchi N, Matsubara R, Isaki K, Torii H

机构信息

Department of Neuropsychiatry, Kanazawa University School of Medicine, Japan.

出版信息

Jpn J Psychiatry Neurol. 1990 Sep;44(3):607-18. doi: 10.1111/j.1440-1819.1990.tb01637.x.

Abstract

The ultrastructure of rectal biopsy specimens from a 60-year-old woman of unusual familial ataxia with cerebrospinal fluid abnormality was investigated. She had two male siblings similarly affected and a close consanguinity in the family. Meissner's plexus neurons, Schwann cells, fibroblasts and smooth muscle cells within the rectum contained intracytoplasmic eosinophilic inclusions (IEIs) with or without intensely eosinophilic granules. Ultrastructurally the IEIs were composed of a membrane-bound, fine granular material with or without dense cores. The IEIs resembled intracytoplasmic inclusions seen in various cells of the central nervous system from a male autopsied sibling. The clinically and morphologically similar finding in the two siblings suggests an autosomal recessive inherited metabolic disorder previously unreported.

摘要

对一名患有异常家族性共济失调且脑脊液异常的60岁女性的直肠活检标本进行了超微结构研究。她有两个同样患病的男性兄弟姐妹,且家族中有近亲结婚情况。直肠内的迈斯纳神经丛神经元、施万细胞、成纤维细胞和平滑肌细胞含有胞质内嗜酸性包涵体(IEIs),有的伴有嗜酸性强的颗粒。超微结构上,IEIs由膜结合的细颗粒物质组成,有的有致密核心,有的没有。这些IEIs类似于在一名男性同胞尸检时发现的中枢神经系统各种细胞中的胞质内包涵体。两名兄弟姐妹在临床和形态学上的相似发现提示一种先前未报道的常染色体隐性遗传代谢障碍。

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