Hypomania in Bobble-Head Doll Syndrome: A Case Report of Surgically Treated Stereotypy and Hypomania
Psychiatry Investigation
;
: 546-549, 2018.
Artículo
en Inglés
| WPRIM
| ID: wpr-714716
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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Aracnoides
/
Recurrencia
/
Trastorno Bipolar
/
Encéfalo
/
Imagen por Resonancia Magnética
/
Estudios de Seguimiento
/
Quistes Aracnoideos
/
Movimientos de la Cabeza
/
Tercer Ventrículo
/
Enfermedades Raras
Tipo de estudio:
Estudio observacional
/
Estudio pronóstico
Límite:
Humanos
Idioma:
Inglés
Revista:
Psychiatry Investigation
Año:
2018
Tipo del documento:
Artículo
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