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一名80岁男性的点头娃娃综合征,与四叠体板巨大蛛网膜囊肿相关,采用内镜下脑室囊肿脑池造瘘术和囊肿腹腔分流术治疗。

Bobble-head doll syndrome in an 80-year-old man, associated with a giant arachnoid cyst of the lamina quadrigemina, treated with endoscopic ventriculocystocisternotomy and cystoperitoneal shunt.

作者信息

Olvera-Castro Jorge Octavio, Morales-Briceño Hugo, Sandoval-Bonilla Bayron, Gallardo-Ceja David, Venegas-Cruz Miguel Angel, Estrada-Estrada Eric Misael, Contreras-Mota Marisol, Guinto-Balanzar Gerardo, Garcia-Lopez Rabindranath

机构信息

Department of Neurosurgery, Hospital de Especialidades del Centro Medico Nacional Siglo XXI, Mexico City, Mexico.

Department of Neurology, Hospital de Especialidades del Centro Medico Nacional Siglo XXI, Mexico City, Mexico.

出版信息

Acta Neurochir (Wien). 2017 Aug;159(8):1445-1450. doi: 10.1007/s00701-017-3195-z. Epub 2017 May 9.

DOI:10.1007/s00701-017-3195-z
PMID:28488069
Abstract

Bobble-head doll syndrome (BHDS) is a rare entity, characterized by antero-posterior head bobbing, which is of the type "yes-yes." Less frequently, having a head movement of the type "no-no" is described. We report an unusual case of an 80-year-old man with a cystic mass of the lamina quadrigemina, extending to the posterior fossa. We conclude that ventriculocystocisternotomy associated with a cystoperitoneal shunt is an effective treatment for a symptomatic giant arachnoid cyst in the lamina quadrigemina.

摘要

点头娃娃综合征(BHDS)是一种罕见病症,其特征为头部呈“是-是”型的前后摆动。较少见的情况下,也有描述头部呈“否-否”型运动的情况。我们报告了一例不寻常的病例,一名80岁男性,其四叠体板有一个囊性肿块,并延伸至后颅窝。我们得出结论,脑室囊肿脑池造瘘术联合囊肿-腹腔分流术是治疗四叠体板有症状的巨大蛛网膜囊肿的有效方法。

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Bobble-head doll syndrome in an 80-year-old man, associated with a giant arachnoid cyst of the lamina quadrigemina, treated with endoscopic ventriculocystocisternotomy and cystoperitoneal shunt.一名80岁男性的点头娃娃综合征,与四叠体板巨大蛛网膜囊肿相关,采用内镜下脑室囊肿脑池造瘘术和囊肿腹腔分流术治疗。
Acta Neurochir (Wien). 2017 Aug;159(8):1445-1450. doi: 10.1007/s00701-017-3195-z. Epub 2017 May 9.
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"No-no" type bobble-head doll syndrome in an infant with an arachnoid cyst of the posterior fossa: a case report.后颅窝蛛网膜囊肿患儿的“摇头娃娃”综合征 1 例报告。
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Bobble-head doll syndrome in an infant with an arachnoid cyst: a case report.婴儿蛛网膜囊肿伴玩偶头综合征 1 例报告。
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An unusual presentation of bobble-head doll syndrome in a patient with hydranencephaly and Chiari 3 malformation.一名患有积水性无脑畸形和Chiari 3型畸形的患者出现了点头娃娃综合征的罕见表现。
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Bobble-head doll syndrome successfully treated with an endoscopic ventriculocystocisternostomy. Case report and review of the literature.采用内镜下脑室-囊肿-脑池造瘘术成功治疗点头娃娃综合征。病例报告及文献复习
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引用本文的文献

1
An unusual presentation of bobble-head doll syndrome in a patient with hydranencephaly and Chiari 3 malformation.一名患有积水性无脑畸形和Chiari 3型畸形的患者出现了点头娃娃综合征的罕见表现。
Childs Nerv Syst. 2019 May;35(5):879-882. doi: 10.1007/s00381-019-04054-x. Epub 2019 Feb 6.