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Parkinson’s Disease and Bipolar Disorder: a case report and narrative review

Published online by Cambridge University Press:  01 September 2022

H. Andreu Gracia*
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
L. Ilzarbe
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
O. Marco Estrada
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
L. Bueno Sanya
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
O. De Juan Viladegut
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
L. Olivier Mayorga
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
L. Pintor
Affiliation:
Hospital Clínic de Barcelona, Consultation Liaison Psychiatry, Barcelona, Spain
F. Valldeoriola
Affiliation:
Hospital Clínic de Barcelona, Neurology, Barcelona, Spain
I. Grande
Affiliation:
Hospital Clínic de Barcelona, Psychiatry, Barcelona, Spain
*
*Corresponding author.

Abstract

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Introduction

Bipolar disorder (BD) is considered a risk factor for developing Parkinson’s Disease (PD) because of an altered dopamine activity in both entities. Comorbidity may delay diagnosis and difficult therapeutic management.

Objectives

To describe the case of a patient with both BD and PD and to determine the appropriate diagnostic and therapeutic approach for patients presenting both entities.

Methods

We present the case of a 58-year-old woman attended in our neurology unit due to the initial presence of visual hallucinations as a core symptom.

Results

Psychotic symptoms as hallucinations and off-times, frequently observed in PD, may be misdiagnosed with a worsening of depressive polarity of BD. Thus, overlap between symptoms may lead to a challenging differential diagnosis. Moreover, there is no consensus about the therapeutic management of the comorbidity, due to the bidirectional worsening of symptoms when treatment is adjusted. In our case, a diagnosis of dopaminergic psychosis was made so antipsychotic treatment with quetiapine 50 mg/d was initiated. A worsening of symptoms was observed, presenting the patient a stuporous status, mutism and generalized rigidity. Neuroimaging and lumbar puncture were performed showing no alterations; electroencephalogram showed diffuse slowing. Final diagnosis was an off-episode of PD and a multifactorial encephalopathy resulting in visual hallucinations.

Conclusions

Coexistence of PD and BD may lead to a diagnostic and therapeutic delay and therefore a worse prognosis. Although these diseases are well-known, it is still challenging to manage patients presenting both entities. Further research is needed to clarify the proper diagnostic and therapeutic approach for these patients.

Disclosure

No significant relationships.

Type
Abstract
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of the European Psychiatric Association
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