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Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report

INTRODUCTION: Tuberous sclerosis is a multisystem genetic disorder. It is associated with significant psychiatric comorbidity mainly autistic disorders, hyperkinetic disorders, depression and anxiety. It is rarely associated with psychosis and bipolar disorder. OBJECTIVES: To describe the case of a...

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Autores principales: Santos, M., Ferreira, T., Neves, P., Peres, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567892/
http://dx.doi.org/10.1192/j.eurpsy.2022.2278
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author Santos, M.
Ferreira, T.
Neves, P.
Peres, J.
author_facet Santos, M.
Ferreira, T.
Neves, P.
Peres, J.
author_sort Santos, M.
collection PubMed
description INTRODUCTION: Tuberous sclerosis is a multisystem genetic disorder. It is associated with significant psychiatric comorbidity mainly autistic disorders, hyperkinetic disorders, depression and anxiety. It is rarely associated with psychosis and bipolar disorder. OBJECTIVES: To describe the case of a 34-year-old male with concomitant diagnosis of bipolar disorder and tuberous sclerosis. METHODS: Case report based on clinical records. Brief literature review using articles searched in the PubMed/MEDLINE database using the terms “tuberous sclerosis”, “bipolar disorder” and “neuropsychiatric”. RESULTS: The patient presented at our Emergency Department 3 years ago with a mixed episode with psychotic symptoms with 1 month of duration. Prior history of two hypomanic episodes, but no depressive episodes. High baseline functionality. Sporadic use of alcohol and cannabis. No family history of psychiatric or neurological diseases. Diagnostic work-up showed no relevant results, aside from small calcifications in brain CT. He was admitted to our ward and medicated with aripiprazol (titrated up to 30 mg), leading to full remission of the clinical picture. The patient was referred to our outpatient clinic and stayed with medication for 1,5 years. One year after, he presented a sudden episode of mutism and perplexity with quick remission. The EEG wielded no relevant results. New brain CT showed signs of tuberous sclerosis. He was referred to Neurology and subsequent assessments, including brain MRI, led to the fulfilment of clinical criteria for tuberous sclerosis. CONCLUSIONS: This case illustrates the possibility of concomitant diagnosis of bipolar disorder and tuberous sclerosis. The possible association between these disorders is discussed. DISCLOSURE: No significant relationships.
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spelling pubmed-95678922022-10-17 Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report Santos, M. Ferreira, T. Neves, P. Peres, J. Eur Psychiatry Abstract INTRODUCTION: Tuberous sclerosis is a multisystem genetic disorder. It is associated with significant psychiatric comorbidity mainly autistic disorders, hyperkinetic disorders, depression and anxiety. It is rarely associated with psychosis and bipolar disorder. OBJECTIVES: To describe the case of a 34-year-old male with concomitant diagnosis of bipolar disorder and tuberous sclerosis. METHODS: Case report based on clinical records. Brief literature review using articles searched in the PubMed/MEDLINE database using the terms “tuberous sclerosis”, “bipolar disorder” and “neuropsychiatric”. RESULTS: The patient presented at our Emergency Department 3 years ago with a mixed episode with psychotic symptoms with 1 month of duration. Prior history of two hypomanic episodes, but no depressive episodes. High baseline functionality. Sporadic use of alcohol and cannabis. No family history of psychiatric or neurological diseases. Diagnostic work-up showed no relevant results, aside from small calcifications in brain CT. He was admitted to our ward and medicated with aripiprazol (titrated up to 30 mg), leading to full remission of the clinical picture. The patient was referred to our outpatient clinic and stayed with medication for 1,5 years. One year after, he presented a sudden episode of mutism and perplexity with quick remission. The EEG wielded no relevant results. New brain CT showed signs of tuberous sclerosis. He was referred to Neurology and subsequent assessments, including brain MRI, led to the fulfilment of clinical criteria for tuberous sclerosis. CONCLUSIONS: This case illustrates the possibility of concomitant diagnosis of bipolar disorder and tuberous sclerosis. The possible association between these disorders is discussed. DISCLOSURE: No significant relationships. Cambridge University Press 2022-09-01 /pmc/articles/PMC9567892/ http://dx.doi.org/10.1192/j.eurpsy.2022.2278 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Abstract
Santos, M.
Ferreira, T.
Neves, P.
Peres, J.
Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
title Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
title_full Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
title_fullStr Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
title_full_unstemmed Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
title_short Concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
title_sort concomitant diagnosis of bipolar disorder and tuberous sclerosis - a case report
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567892/
http://dx.doi.org/10.1192/j.eurpsy.2022.2278
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