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慢性特发性共济失调性神经病:一例神经病理学研究

Chronic idiopathic ataxic neuropathy: neuropathology of a case.

作者信息

Simon L T, Ricaurte G A, Forno L S

机构信息

Department of Neurology, Veterans Administration Medical Center, Palo Alto, CA 94304.

出版信息

Acta Neuropathol. 1989;79(1):104-7. doi: 10.1007/BF00308965.

Abstract

A case of chronic, sporadic, slowly progressive, purely sensory, ataxic neuropathy is reported. In previously published similar cases only muscle and nerve biopsies have been available for study. In the present case the patient died of an unrelated illness 39 years after onset of the neuropathy. A full neuropathological study was performed. The disease process was limited to the dorsal root ganglia and their central and peripheral processes. Large myelinated fibers were preferentially involved. Involvement of the dorsal root ganglia has also been reported in certain toxic ganglioneuropathies and in the sensory neuropathy associated with carcinoma. The long duration and insidious development set the present case apart from those conditions. An inflammatory component was lacking. Except for a microscopic focus of adenocarcinoma of the prostate no malignancy was present. The etiology of chronic idiopathic ataxic neuropathy is unknown, but it is likely that the dorsal root ganglion is the main target for the disease process in most if not all cases.

摘要

报告了一例慢性、散发性、缓慢进展的纯感觉性共济失调性神经病。在先前发表的类似病例中,仅有肌肉和神经活检可供研究。在本病例中,患者在神经病发病39年后死于无关疾病。进行了全面的神经病理学研究。疾病过程局限于背根神经节及其中枢和周围神经纤维。大的有髓纤维优先受累。在某些中毒性神经节病和与癌症相关的感觉神经病中也有背根神经节受累的报道。本病例病程长且隐匿性发展,与那些疾病不同。缺乏炎症成分。除前列腺腺癌的一个微观病灶外,未发现恶性肿瘤。慢性特发性共济失调性神经病的病因尚不清楚,但在大多数(如果不是全部)病例中,背根神经节很可能是疾病过程的主要靶点。

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