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继发于恶性纤维组织细胞瘤的副肿瘤性共济失调和肌张力障碍。

Paraneoplastic ataxia and dystonia secondary to a malignant fibrous histiocytoma.

作者信息

Dolan Ross, Thomas Ralph, O'Riordan Jonathan I

机构信息

Department of Neurology, University of Dundee, Dundee, UK.

出版信息

BMJ Case Rep. 2010 Nov 12;2010:bcr0520102983. doi: 10.1136/bcr.05.2010.2983.

Abstract

Paraneoplastic movement disorders are part of the spectrum of paraneoplastic syndromes caused by the production of onconeural antibodies such as anti-Hu by underlying tumours. These attack specific neurons depending on receptor aetiology. We report the case of a 53-year-old man who presented 8 years previously with symptoms of upper limb weakness, light headedness, dizziness and falls. His condition followed a progressive course. Two years after onset he had right-sided weakness, diplopia and generalised dystonia. Initial investigations identified a positive anti-Hu antibody, but an extensive search for a primary tumour was negative. A malignant fibrous histiocytoma in his right gluteal fold was subsequently identified. At this stage he was bed bound with severe ataxia, dystonia and spasticity. Following surgical excision and treatment with high dose steroids and pulse immunoglobulin, further progression was arrested and minor improvements occurred. He can now ambulate with bilateral assistance but remains severely disabled.

摘要

副肿瘤性运动障碍是由潜在肿瘤产生抗Hu等肿瘤神经抗体所引起的副肿瘤综合征谱系的一部分。这些抗体根据受体病因攻击特定神经元。我们报告一例53岁男性病例,他8年前出现上肢无力、头晕、眩晕和跌倒症状。其病情呈进行性发展。发病两年后,他出现右侧肢体无力、复视和全身性肌张力障碍。初步检查发现抗Hu抗体呈阳性,但广泛寻找原发肿瘤结果为阴性。随后在其右臀皱襞处发现了恶性纤维组织细胞瘤。此时,他因严重共济失调、肌张力障碍和痉挛而卧床不起。经过手术切除、大剂量类固醇治疗和静脉注射免疫球蛋白后,病情进一步进展得到控制,并有轻微改善。他现在在双侧辅助下可以行走,但仍然严重残疾。

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本文引用的文献

1
Paraneoplastic movement disorders.副肿瘤性运动障碍
Mov Disord. 2009 Sep 15;24(12):1715-24. doi: 10.1002/mds.22658.
2
[Paraneoplastic disorders of the nervous system].[神经系统副肿瘤性疾病]
Rinsho Shinkeigaku. 2008 Nov;48(11):799-803. doi: 10.5692/clinicalneurol.48.799.
3
Paraneoplastic neurological syndromes.副肿瘤性神经系统综合征
Orphanet J Rare Dis. 2007 May 4;2:22. doi: 10.1186/1750-1172-2-22.

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