A Rare Presentation of Catatonia due to Primary Adrenal Insufficiency

If you need an accessible version of this item, please email your request to digschol@iu.edu so that they may create one and provide it to you.
Date
2019
Language
English
Embargo Lift Date
Committee Members
Degree
Degree Year
Department
Grantor
Journal Title
Journal ISSN
Volume Title
Found At
Elsevier
Abstract

Primary adrenal insufficiency (PAI), also called Addison’s disease, is an endocrine disorder in which the adrenal glands are unable to produce an adequate amount of glucocorticoids and/or mineralcorticoids. Acute adrenal insufficiency can present with neuropsychiatric symptoms including depression, anxiety, cognitive complaints, and changes in mental status progressing from decreased responsiveness to stupor and coma(1). It has been estimated that the prevalence of neuropsychiatric symptoms in PAI ranges from 64-84%. Though there are no case reports in the recent literature, catatonia has been associated with PAI in historical case reports(2). Therefore, PAI as a cause of catatonia may be under-recognized by psychiatrists and endocrinologists. As PAI can be potentially life threatening, it is important for the consultation-liaison psychiatrist to be able to recognize the condition in the context of vague, nonspecific neuropsychiatric complaints. Here, we present a case of catatonia presenting secondary to PAI and review the literature of neuropsychiatric symptoms associated with PAI.

Description
item.page.description.tableofcontents
item.page.relation.haspart
Cite As
Puzanov, M., Davis, H., & Holmes, E. G. (2019). A Rare Presentation of Catatonia due to Primary Adrenal Insufficiency. Psychosomatics. https://doi.org/10.1016/j.psym.2019.02.008
ISSN
Publisher
Series/Report
Sponsorship
Major
Extent
Identifier
Relation
Journal
Psychosomatics
Source
Author
Alternative Title
Type
Article
Number
Volume
Conference Dates
Conference Host
Conference Location
Conference Name
Conference Panel
Conference Secretariat Location
Version
Author's manuscript
Full Text Available at
This item is under embargo {{howLong}}