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

被引：1

作者：

Hahm, Myong Hun ^{[1
]}

Woo, Jungmin ^{[2
]}

Kim, Ki Hong ^{[3
]}

机构：

[1] Kyungpook Natl Univ, Sch Med, Dept Radiol, Daegu, South Korea

[2] Kyungpook Natl Univ, Sch Med, Dept Psychiat, 680 Gukchaebosang Ro, Daegu 41944, South Korea

[3] Catholic Univ Daegu, Sch Med, Dept Neurosurg, Daegu, South Korea

来源：

PSYCHIATRY INVESTIGATION | 2018年 / 15卷 / 05期

关键词：

Arachnoid cysts; Bobble-head doll syndrome; Mania; Stereotypy; OF-THE-LITERATURE; ARACHNOID CYST; BIPOLAR DISORDER; FUNCTIONAL NEUROANATOMY;

D O I：

10.30773/pi.2017.10.25.2

中图分类号：

R749 [精神病学];

学科分类号：

100205 ;

摘要：

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 ease of bobble-head doll syndrome and discuss the possible neuropsychiatric mechanisms of this rare disease.

引用

页码：546 / 549

页数：4

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