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[进行性自主神经功能障碍作为抗Hu抗体相关综合征的初始表现]

[Progressive dysautonomia as initial manifestation of anti-Hu antibody-related syndrome].

作者信息

Palao S, Corral I, Vera R, Alonso de Leciñana M

机构信息

Servicio de Neurología. Hospital Ramón y Cajal. Madrid, Spain.

出版信息

Neurologia. 2007 Dec;22(10):899-902.

Abstract

INTRODUCTION

The anti-Hu antibody are associated with central nervous system paraneoplastic syndromes such as sensory neuropathy, cerebellar ataxia or limbic encephalitis. The isolated autonomic dysfunction as the presenting manifestation of anti-Hu antibody-related paraneoplastic syndrome is extremely infrequent.

CASE REPORT

A 68 year-old male presented with a two-month history of severe constipation following of orthostatic hypotension, impotence, urinary retention and intestinal pseudo-obstruction as manifestations of progressive dysautonomia. Four months after the onset of these symptoms, he developed paresthesias in the hands and feet, motor weakness in both upper and lower limbs and ophtalmoplegia. Anti-Hu antibodies were positive in serum and cerebrospinal fluid, although tumor was not found.

CONCLUSIONS

Progressive dysautonomia may result from a number of diseases. We encourage to consider also the possibility of anti-Hu antibody-related syndrome, despite the case that it is a very unusual isolated initial manifestation.

摘要

引言

抗Hu抗体与中枢神经系统副肿瘤综合征相关,如感觉神经病变、小脑共济失调或边缘性脑炎。以孤立性自主神经功能障碍作为抗Hu抗体相关副肿瘤综合征的首发表现极为罕见。

病例报告

一名68岁男性,有两个月严重便秘病史,继之以体位性低血压、阳痿、尿潴留和肠道假性梗阻,为进行性自主神经功能障碍的表现。这些症状出现四个月后,他出现手足感觉异常、双上肢和双下肢运动无力以及眼肌麻痹。血清和脑脊液中抗Hu抗体呈阳性,尽管未发现肿瘤。

结论

进行性自主神经功能障碍可能由多种疾病引起。尽管抗Hu抗体相关综合征以这种非常不寻常的孤立首发表现出现的情况很少见,但我们仍建议考虑其可能性。

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