An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment
Here we report a case of a 15-year-old female who had originally been diagnosed and treated unsuccessfully for schizophrenia, psychosis, severe anxiety, and depression. More in-depth history revealed an abrupt onset of her symptoms with remote acute infections and many exhibited characteristics of o...
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Series: | Case Reports in Psychiatry |
Online Access: | http://dx.doi.org/10.1155/2018/8189067 |
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doaj-e1adc0543f7f4e05a7ec07ac62d242572020-11-24T22:20:06ZengHindawi LimitedCase Reports in Psychiatry2090-682X2090-68382018-01-01201810.1155/2018/81890678189067An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis TreatmentDrew H. Barzman0Hannah Jackson1Umesh Singh2Marcus Griffey3Michael Sorter4Jonathan A. Bernstein5University of Cincinnati College of Medicine, Department of Psychiatry and Behavioral Neuroscience, CARE/Crawley Building, Suite E-870 3230 Eden Avenue Cincinnati, OH 45267, USACincinnati Children’s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3026, USAUniversity of Cincinnati College of Medicine, Division of Immunology Allergy Section, 231 Albert Sabin Way, Cincinnati, OH 45267, USACincinnati Children’s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3026, USACincinnati Children’s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3026, USAUniversity of Cincinnati College of Medicine, Division of Immunology Allergy Section, 231 Albert Sabin Way, Cincinnati, OH 45267, USAHere we report a case of a 15-year-old female who had originally been diagnosed and treated unsuccessfully for schizophrenia, psychosis, severe anxiety, and depression. More in-depth history revealed an abrupt onset of her symptoms with remote acute infections and many exhibited characteristics of obsessive compulsive disorder with rituals. Work-up for underlying infectious, immunodeficiency, and autoimmune causes was unrevealing except for very high levels of anti-neuronal antibodies which have been linked to Pediatric Acute-onset Neuropsychiatric Syndrome (PANS). Treatment options were discussed with the family and it was decided to use a course of plasmapheresis based on previous studies demonstrating efficacy and its safety profile. After course of therapy, there was a dramatic resolution of her psychosis, OCD traits, and anxiety. She was able to stop all of her antipsychotic and anxiety medications and resume many of her previous normal daily activities. The effect of this treatment has been sustained to the present time. This case emphasizes the importance of exploring nontraditional treatments for severe, treatment-resistant mental illness which requires a multidisciplinary approach. Further research is warranted in larger populations to investigate pathomechanisms and treatment of PANs/PANDAs.http://dx.doi.org/10.1155/2018/8189067 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Drew H. Barzman Hannah Jackson Umesh Singh Marcus Griffey Michael Sorter Jonathan A. Bernstein |
spellingShingle |
Drew H. Barzman Hannah Jackson Umesh Singh Marcus Griffey Michael Sorter Jonathan A. Bernstein An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment Case Reports in Psychiatry |
author_facet |
Drew H. Barzman Hannah Jackson Umesh Singh Marcus Griffey Michael Sorter Jonathan A. Bernstein |
author_sort |
Drew H. Barzman |
title |
An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment |
title_short |
An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment |
title_full |
An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment |
title_fullStr |
An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment |
title_full_unstemmed |
An Atypical Presentation of Pediatric Acute Neuropsychiatric Syndrome Responding to Plasmapheresis Treatment |
title_sort |
atypical presentation of pediatric acute neuropsychiatric syndrome responding to plasmapheresis treatment |
publisher |
Hindawi Limited |
series |
Case Reports in Psychiatry |
issn |
2090-682X 2090-6838 |
publishDate |
2018-01-01 |
description |
Here we report a case of a 15-year-old female who had originally been diagnosed and treated unsuccessfully for schizophrenia, psychosis, severe anxiety, and depression. More in-depth history revealed an abrupt onset of her symptoms with remote acute infections and many exhibited characteristics of obsessive compulsive disorder with rituals. Work-up for underlying infectious, immunodeficiency, and autoimmune causes was unrevealing except for very high levels of anti-neuronal antibodies which have been linked to Pediatric Acute-onset Neuropsychiatric Syndrome (PANS). Treatment options were discussed with the family and it was decided to use a course of plasmapheresis based on previous studies demonstrating efficacy and its safety profile. After course of therapy, there was a dramatic resolution of her psychosis, OCD traits, and anxiety. She was able to stop all of her antipsychotic and anxiety medications and resume many of her previous normal daily activities. The effect of this treatment has been sustained to the present time. This case emphasizes the importance of exploring nontraditional treatments for severe, treatment-resistant mental illness which requires a multidisciplinary approach. Further research is warranted in larger populations to investigate pathomechanisms and treatment of PANs/PANDAs. |
url |
http://dx.doi.org/10.1155/2018/8189067 |
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