Neurodegeneration with brain iron accumulation associated with late-onset psychiatric symptoms

Authors

  • Júlio César Claudino dos Santos Universidade Federal de São Paulo, UNIFESP, São Paulo, SP, Brasil https://orcid.org/0000-0001-6543-481X
  • Luiza Sarsur Ribeiro Pontíficia Universidade Católica de Minas Gerais, PUC, Belo Horizonte, Minas Gerais, Brasil https://orcid.org/0000-0001-7403-1932
  • Rafaella Iughetti da Costa Centro Universitário Christus, Unichristus, Fortaleza, CE, Brasil. https://orcid.org/0000-0001-8723-7892
  • Eduardo Bordignon Peccin Centro de Estudos José de Barros Falcão, CEJBF, Porto Alegre, RS, Brasil https://orcid.org/0000-0002-2927-4449
  • Paulo Andre Pera Grabowski Preceptor do Serviço de Psiquiatria do Hospital San Julian, Curitiba, PR, Brasil.

DOI:

https://doi.org/10.25118/2763-9037.2022.v12.386

Keywords:

neurodegeneration, brain iron accumulation, NBIA, PKAN2

Abstract

Introduction: The neurodegeneration with brain iron accumulation (NBIA) is a heterogeneous group of rare genetic disorders that lead to accumulation of iron in the basal nuclei, which leads to numerous neurologic disorders. This condition has been associated with many genes, PKAN2 being the most common. The treatment remains mostly symptomatic and the approach based on a multidisciplinary team is recommended. Case report: The case presented is from a 67-year-old male with iron accumulation bilaterally in the pale globes and has been having delirium for 8 months, as well as visuospatial and executive dysfunction and behavioral alterations. The patient's MRI showed abnormalities and the “eye of the tiger” sign. Furthemore, the treatment of choice was the administration of atypical antipsychotic medication, which partially controlled the patient's condition. Discussion: The most recurrent location of brain iron accumulation is in the basal ganglia and it is mainly linked with mutations in the pantothenate kinase 2 (PKAN2), which leads to psychiatric manifestations of insidious progression and can be inferred when the “eye of the tiger” sign is found in a MRI. Conclusion: The patient was diagnosed with late onset psychotic disorder, mild cognitive deficit and parkisonian syndrome. Genetic tests were not performed to diagnose the etiology. Therefore, the case is considered a NBIA of unknown cause with atypical characteristics and probable mutation linked to PANK2.




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Author Biographies

Júlio César Claudino dos Santos, Universidade Federal de São Paulo, UNIFESP, São Paulo, SP, Brasil

Luiza Sarsur Ribeiro, Pontíficia Universidade Católica de Minas Gerais, PUC, Belo Horizonte, Minas Gerais, Brasil

Rafaella Iughetti da Costa, Centro Universitário Christus, Unichristus, Fortaleza, CE, Brasil.

Eduardo Bordignon Peccin, Centro de Estudos José de Barros Falcão, CEJBF, Porto Alegre, RS, Brasil

Paulo Andre Pera Grabowski, Preceptor do Serviço de Psiquiatria do Hospital San Julian, Curitiba, PR, Brasil.

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Published

2022-08-13

How to Cite

1.
Santos JCC dos, Ribeiro LS, Costa RI da, Peccin EB, Grabowski PAP. Neurodegeneration with brain iron accumulation associated with late-onset psychiatric symptoms. Debates em Psiquiatria [Internet]. 2022 Aug. 13 [cited 2025 Feb. 5];12:1-11. Available from: https://revistardp.org.br/revista/article/view/386

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