• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Hypomania in Bobble-Head Doll Syndrome: A Case Report of Surgically Treated Stereotypy and Hypomania.

作者信息

Hahm Myong Hun, Woo Jungmin, Kim Ki Hong

机构信息

Department of Radiology, School of Medicine, Kyungpook National University, Daegu, Repubic of Korea.

Department of Psychiatry, School of Medicine, Kyungpook National University, Daegu, Repubic of Korea.

出版信息

Psychiatry Investig. 2018 May;15(5):546-549. doi: 10.30773/pi.2017.10.25.2. Epub 2018 Mar 30.

DOI:10.30773/pi.2017.10.25.2
PMID:29593205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5976000/
Abstract

A 22-year-old man was admitted with gradually aggravating stereotypic head movement with hypomania. Brain magnetic resonance imaging showed a large suprasellar arachnoid cyst extending into the third ventricle, with obstructive hydrocephalus, characteristic of bobble-head doll syndrome. Endoscopic fenestration of the suprasellar arachnoid cyst was performed. Stereotypic head movement stopped immediately after surgery and hypomanic symptoms gradually improved within a month. During 4 years of follow-up observation without medication, neuropsychiatric symptoms did not relapse. We report our experience of surgically treating stereotypy and hypomania in a case of bobble-head doll syndrome and discuss the possible neuropsychiatric mechanisms of this rare disease.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df6e/5976000/8e6da575b8ce/pi-2017-10-25-2f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df6e/5976000/36ab5c30a605/pi-2017-10-25-2f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df6e/5976000/8e6da575b8ce/pi-2017-10-25-2f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df6e/5976000/36ab5c30a605/pi-2017-10-25-2f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df6e/5976000/8e6da575b8ce/pi-2017-10-25-2f2.jpg

相似文献

1
Hypomania in Bobble-Head Doll Syndrome: A Case Report of Surgically Treated Stereotypy and Hypomania.
Psychiatry Investig. 2018 May;15(5):546-549. doi: 10.30773/pi.2017.10.25.2. Epub 2018 Mar 30.
2
Suprasellar arachnoid cyst presenting with bobble-head doll syndrome: Report of three cases.鞍上蛛网膜囊肿伴点头娃娃综合征:三例报告
J Pediatr Neurosci. 2015 Jan-Mar;10(1):18-21. doi: 10.4103/1817-1745.154321.
3
"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。
Pediatr Neurol. 2013 Dec;49(6):474-6. doi: 10.1016/j.pediatrneurol.2013.07.013. Epub 2013 Sep 26.
4
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。
J Med Case Rep. 2022 Oct 28;16(1):393. doi: 10.1186/s13256-022-03623-0.
5
Suprasellar Cyst Presenting With Bobble-Head Doll Syndrome.鞍上囊肿伴玩偶头综合征。
World Neurosurg. 2020 Jan;133:80-83. doi: 10.1016/j.wneu.2019.09.131. Epub 2019 Sep 28.
6
Navigated laser-assisted endoscopic fenestration of a suprasellar arachnoid cyst in a 2-year-old child with bobble-head doll syndrome. Case report.导航激光辅助内镜下开窗治疗一名患有点头娃娃综合征的2岁儿童鞍上蛛网膜囊肿。病例报告。
J Neurosurg. 2006 May;104(5 Suppl):348-51. doi: 10.3171/ped.2006.104.5.348.
7
Bobble-head doll syndrome: report of 2 cases and a review of the literature, with video documentation of the clinical phenomenon.点头娃娃综合征:2例报告及文献复习,并附该临床现象的视频资料
J Neurosurg Pediatr. 2018 Mar;21(3):236-246. doi: 10.3171/2017.9.PEDS16704. Epub 2018 Jan 5.
8
Suprasellar arachnoid cyst presenting with bobble-head doll movements: a report of 3 cases.鞍上蛛网膜囊肿伴点头娃娃样动作:3例报告
Neurol India. 2003 Sep;51(3):407-9.
9
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.
10
Bobble-head doll syndrome due to a suprasellar arachnoid cyst: endoscopic treatment in two cases.鞍上蛛网膜囊肿所致点头娃娃综合征:两例内镜治疗
Childs Nerv Syst. 2004 Oct;20(10):770-3. doi: 10.1007/s00381-004-0925-3.

引用本文的文献

1
Bobble head doll syndrome (BHDS): Case report.点头娃娃综合征(BHDS):病例报告。
Radiol Case Rep. 2023 May 13;18(7):2498-2502. doi: 10.1016/j.radcr.2023.04.008. eCollection 2023 Jul.
2
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.

本文引用的文献

1
Suprasellar arachnoid cyst presenting with bobble-head doll syndrome: Report of three cases.鞍上蛛网膜囊肿伴点头娃娃综合征:三例报告
J Pediatr Neurosci. 2015 Jan-Mar;10(1):18-21. doi: 10.4103/1817-1745.154321.
2
"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。
Pediatr Neurol. 2013 Dec;49(6):474-6. doi: 10.1016/j.pediatrneurol.2013.07.013. Epub 2013 Sep 26.
3
Functional neuroanatomy of bipolar disorder: structure, function, and connectivity in an amygdala-anterior paralimbic neural system.
双相情感障碍的功能神经解剖学:杏仁核-前边缘系统神经网络的结构、功能和连接。
Bipolar Disord. 2012 Jun;14(4):340-55. doi: 10.1111/j.1399-5618.2012.01015.x.
4
Emotion processing and regulation in bipolar disorder: a review.双相障碍中的情绪加工和调节:综述。
Bipolar Disord. 2012 Jun;14(4):326-39. doi: 10.1111/j.1399-5618.2012.01021.x.
5
The functional neuroanatomy of bipolar disorder: a consensus model.双相障碍的功能神经解剖学:共识模型。
Bipolar Disord. 2012 Jun;14(4):313-25. doi: 10.1111/j.1399-5618.2012.01022.x.
6
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
J Neurosurg. 2005 Sep;103(3 Suppl):253-9. doi: 10.3171/ped.2005.103.3.0253.
7
Suprasellar arachnoid cyst presenting with bobble-head doll movements: a report of 3 cases.鞍上蛛网膜囊肿伴点头娃娃样动作:3例报告
Neurol India. 2003 Sep;51(3):407-9.
8
Bobble-head doll syndrome: some atypical features with a new lesion and review of the literature.
Acta Neurol Scand. 2003 Sep;108(3):216-20. doi: 10.1034/j.1600-0404.2003.00101.x.
9
Bobble-head doll syndrome associated with subduroperitoneal shunt malfunction.
Childs Nerv Syst. 1997 Apr;13(4):234-7. doi: 10.1007/s003810050074.
10
The bobble-head doll syndrome: experimental study of anatomic basis.
Surg Forum. 1974;25(0):466-8.