de Brito Henriques José Gilberto, Henriques Karina Santos Wandeck, Filho Geraldo Pianetti, Fonseca Luiz Fernando, Cardoso Francisco, Da Silva Márcia Cristina
Hospital das Clinicas, Federal University of Minas Gerais, Brazil.
J Neurosurg. 2007 Sep;107(3 Suppl):248-50. doi: 10.3171/PED-07/09/248.
Bobble-head doll syndrome (BHDS) presents in childhood and is usually associated with lesions of the third ventricle. This disorder is characterized by stereotypical head movements of the type "yes-yes" (up and down) at a frequency of 2 to 3 Hz. Rarely, movements of the type "no-no" (side-to-side) are described. There are a few hypotheses to explain the mechanism responsible for BHDS, but its real pathophysiological characteristics are still unknown. The authors describe the case of a child born with hydrocephalus and Dandy-Walker syndrome. A ventriculoperitoneal shunt was implanted in the child because of progressive head enlargement. One year after shunt placement, she began making frequent horizontal head movements of the type "no-no". There were no other signs or symptoms. Imaging studies demonstrated small ventricles and a posterior fossa cyst with no signs of hypertension. The child's growth, development, and head circumference (within the 5th percentile) remained satisfactory. Three aspects of this case were of interest: the association of BHDS with Dandy-Walker syndrome, the rare occurrence of BHDS of the "no-no" type, and the absence of third ventricle dilation. The authors' findings support the hypothesis that cerebellar malformations themselves can
点头娃娃综合征(BHDS)在儿童期出现,通常与第三脑室病变有关。这种疾病的特征是出现频率为2至3赫兹的典型“点头(上下)”样头部运动。很少有描述“摇头(左右)”样运动的情况。有一些假说来解释导致BHDS的机制,但其真正的病理生理特征仍然未知。作者描述了一名患有脑积水和丹迪-沃克综合征的儿童病例。由于头部逐渐增大,该儿童接受了脑室腹腔分流术。分流术后一年,她开始频繁出现“摇头”样的水平头部运动。没有其他体征或症状。影像学研究显示脑室较小且后颅窝有囊肿,无高血压迹象。该儿童的生长、发育和头围(处于第5百分位数)仍令人满意。该病例有三个有趣的方面:BHDS与丹迪-沃克综合征的关联、罕见的“摇头”型BHDS以及第三脑室无扩张。作者的发现支持了小脑畸形本身可以……的假说