波波头娃娃综合症

Yakouba Haro, Sylvain D. Zabsonre, Abdoulaye Sanou, Inoussa Zoungrana, Joseph Biogo, Abel Kabre
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 Observations. Three children, one girl and two boys, aged respectively 5, 9 and 14 years were seen for involuntary abnormal head movements associating lateral rotations assimilated to signs of disapproval (no-no) in two cases, and back and forth movements of the head in one case. In the 14-year-old adolescent, there was also a picture of intracranial hypertension. Clinical examination revealed ataxia and macrocrania in both cases and a syndrome in 1 case. Imaging revealed triventricular hydrocephalus on aqueductal stenosis in all cases with an associated supra sellar cyst in 2 cases. The treatment consisted of endoscopic treatment in 2 cases and ventriculoperitoneal shunt in 1 case. Surgery allowed a considerable regression of involuntary movements of the head in the immediate postoperative period and a complete recovery in the long term.
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摘要

介绍。波波头娃娃综合征是一种神经系统综合征,其特征是头部不自主的异常运动,并在前后方向重复或发作性运动2至3hz,可被理解为赞成运动(是-是),偶尔的侧向旋转可被理解为不赞成信号(否-否)。它是一种罕见的实体,最早由Benton[1]描述。我们描述了布基纳法索Yalgado ousamdrogo大学医院处理的三个病例。观察。三个孩子,一个女孩和两个男孩,年龄分别为5岁,9岁和14岁,观察到不自主的头部异常运动,其中两个病例与侧面旋转同化为不赞成的迹象(no-no),一个病例头部来回运动。在14岁的青少年中,也有颅内高压的图片。临床检查均发现共济失调和大颅畸形,1例伴有综合征。影像学显示所有病例均伴有导水管狭窄的三室脑积水,2例伴有鞍上囊肿。治疗包括内镜治疗2例,脑室腹腔分流术1例。手术使患者在术后立即恢复了头部的不自主运动,并在长期内完全恢复。 结论。泡泡头娃娃综合征是一种罕见的实体,与慢性脑积水引起的异常运动有关,其处理得好,早期可获得良好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bobble Head Doll Syndrome
Introduction. Bobble head doll syndrome is a neurological syndrome characterized by abnormal involuntary movements of the head combining repetitive or episodic movements of 2 to 3 Hz back and forth in the anterior-posterior direction that can be assimilated to approval movements (yes-yes) and occasionally lateral rotations that can be assimilated to disapproval signs (no-no). It is a rare entity first described by Benton[1]. We describe three cases managed at the Yalgado Ouédraogo University Hospital in Burkina Faso. Observations. Three children, one girl and two boys, aged respectively 5, 9 and 14 years were seen for involuntary abnormal head movements associating lateral rotations assimilated to signs of disapproval (no-no) in two cases, and back and forth movements of the head in one case. In the 14-year-old adolescent, there was also a picture of intracranial hypertension. Clinical examination revealed ataxia and macrocrania in both cases and a syndrome in 1 case. Imaging revealed triventricular hydrocephalus on aqueductal stenosis in all cases with an associated supra sellar cyst in 2 cases. The treatment consisted of endoscopic treatment in 2 cases and ventriculoperitoneal shunt in 1 case. Surgery allowed a considerable regression of involuntary movements of the head in the immediate postoperative period and a complete recovery in the long term. Conclusion. The bobble head doll syndrome is a rare entity related to the consequences of chronic hydrocephalus responsible for abnormal movements whose management done well and early leads to favourable results.
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