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儿童阵发性自主神经不稳定伴肌张力障碍:脚间池结核瘤的罕见表现

Paroxysmal autonomic instability with dystonia in a child: rare manifestation of an interpeduncular tuberculoma.

作者信息

Singh Deepak Kumar, Singh Neha

机构信息

Department of Neurosurgery, Dr. RML Institute of Medical Sciences, Lucknow, India.

出版信息

Pediatr Neurosurg. 2011;47(4):275-8. doi: 10.1159/000334276. Epub 2012 Feb 22.

Abstract

The term 'paroxysmal autonomic instability with dystonia' was first given for a group of symptoms comprising diaphoresis, intermittent agitation, hypertension, hyperthermia, tachycardia, tachypnea, and extensor posturing. This usually occurs as a complication of severe brain injury and is infrequently reported in cases of cerebral infection. We report a 1-year-old child with intracranial tuberculoma with symptoms of paroxysmal autonomic instability with dystonia. Pertinent literature is reviewed emphasizing pathophysiology and available treatment options.

摘要

“阵发性自主神经功能不稳定伴肌张力障碍”这一术语最初用于描述一组症状,包括多汗、间歇性烦躁、高血压、高热、心动过速、呼吸急促和伸肌姿势。这通常作为重度脑损伤的并发症出现,在脑部感染病例中鲜有报道。我们报告一名1岁患有颅内结核瘤的儿童,出现了阵发性自主神经功能不稳定伴肌张力障碍的症状。本文回顾了相关文献,重点阐述了其病理生理学及可用的治疗方案。

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