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Case Reports in Psychiatry
Volume 2017, Article ID 8164537, 4 pages
Case Report

Obsessive-Compulsive Disorder Associated with Posterior Cranial Fossa Meningioma

Neuropsychiatric Department, Aichi Medical University, Nagakute 480-1195, Japan

Correspondence should be addressed to Nobuyuki Takeuchi; pj.oc.oohay@350majmaj

Received 21 March 2017; Revised 27 April 2017; Accepted 16 May 2017; Published 1 June 2017

Academic Editor: Gwyneth Zai

Copyright © 2017 Nobuyuki Takeuchi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


We report here a patient in whom the effects of a cerebellum mass may have led to development of obsessive-compulsive disorder (OCD). A 33-year-old woman showed symptoms of OCD, including obsessive worry about infection from tainted blood and repetitive confirmation, which worsened during pregnancy. She had comprehension in regard to her illness and no evidence of cognitive dysfunction and did not meet other DSM-5 criteria such as depression. One month after giving childbirth, the symptoms worsened, while headache and dizziness also developed. The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) score was 34. The patient was examined for a headache and a posterior cranial fossa meningioma was found. Following resection of the meningioma, the OCD symptoms were remarkably reduced (Y-BOCS score 10). There is only one previous report of pure OCD associated with a cerebellar mass and the present findings should help to elucidate the mechanism.