J Neurol Surg A Cent Eur Neurosurg 2019; 80(05): 404-408
DOI: 10.1055/s-0039-1685185
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Normal Pressure Hydrocephalus with Primary Presentation of Psychiatric Disturbance: Case Report

Michael Kogan
1   Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences at the University at Buffalo, Buffalo, New York, United States
2   Department of Neurosurgery, Buffalo General Medical Center at Kaleida Health, Buffalo, New York, United States
,
Justice Agyei
1   Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences at the University at Buffalo, Buffalo, New York, United States
2   Department of Neurosurgery, Buffalo General Medical Center at Kaleida Health, Buffalo, New York, United States
,
Kevin J. Cuddahee
2   Department of Neurosurgery, Buffalo General Medical Center at Kaleida Health, Buffalo, New York, United States
,
Kevin J. Gibbons
1   Department of Neurosurgery, Jacobs School of Medicine and Biomedical Sciences at the University at Buffalo, Buffalo, New York, United States
2   Department of Neurosurgery, Buffalo General Medical Center at Kaleida Health, Buffalo, New York, United States
› Author Affiliations
Further Information

Publication History

29 June 2018

17 October 2018

Publication Date:
10 May 2019 (online)

Zoom Image

Abstract

Background and Objective Progressive impairment of cognitive function is a common feature seen in patients with normal pressure hydrocephalus (NPH). Along with cognitive decline, many of the other classic symptoms of NPH are chronic and rarely present with overwhelming anxiety. We report the case of a 63-year-old man who presented with recent primary psychiatric manifestation of severe disabling anxiety and otherwise a minimal change in gait and no urinary disturbance.

Clinical Presentation The patient's work-up consisted of magnetic resonance imaging that showed moderate ventriculomegaly but no findings concerning for acute obstructive hydrocephalus. A single-photon emission computed tomography scan was markedly abnormal with severe hypoperfusion consistent with hydrocephalus. Initially shunting was not advised but was eventually performed after a dramatic response to a large-volume lumbar puncture. After considerable discussion, he underwent elective ventriculoperitoneal shunt placement and had dramatic and sustained improvement in his anxiety.

Conclusion We believe this case report is a unique description of NPH symptomology and might guide future research or clinical decision making.

Author Contributions

Conception and design: Gibbons; Data acquisition: all authors; Data analysis and interpretation: all authors; Drafting the manuscript: Agyei, Kogan; Critically revising the manuscript: all authors; Final approval of the manuscript: all authors.