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在一例患有伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)患者的腓肠神经活检中鉴定特征性血管变化。

Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

作者信息

Schröder J M, Sellhaus B, Jörg J

机构信息

Institute of Neuropathology, Medical Faculty, Technical University Aachen, Germany.

出版信息

Acta Neuropathol. 1995;89(2):116-21. doi: 10.1007/BF00296354.

Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy' (CADASIL) has recently been identified as a hereditary disorder with characteristic fine structural changes of small intracerebral arteries and arterioles. Electron microscopically there are characteristic perivascular deposits of granular electron-dense material resembling immunoglobulin deposits. The present case from a family with four affected members in three successive generations shows that similar vascular changes as described in the central nervous system are present in blood vessels of the sural nerve, although less pronounced and, therefore, affording electron microscopy for their unequivocal detection. Nevertheless it has been shown for the first time that the diagnosis of CADASIL can be verified by a sural nerve biopsy. Occasional focal accumulation of pinocytotic vesicles opposite the granular deposits suggests exocytosis as one of the possible pathomechanisms for their production.

摘要

伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)最近被确认为一种遗传性疾病,其特征是脑内小动脉和微动脉有细微的结构变化。在电子显微镜下,有特征性的血管周围颗粒状电子致密物质沉积,类似于免疫球蛋白沉积。本病例来自一个连续三代中有四名患病成员的家族,结果显示,腓肠神经血管中存在与中枢神经系统中所描述的相似的血管变化,尽管不太明显,因此需要借助电子显微镜才能明确检测到这些变化。然而,首次证明通过腓肠神经活检可以确诊CADASIL。在颗粒状沉积物相对的位置偶尔出现的局灶性胞饮小泡聚集提示胞吐作用是其产生的可能发病机制之一。

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