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...

Full description

Bibliographic Details
Main Authors: Drew H. Barzman, Hannah Jackson, Umesh Singh, Marcus Griffey, Michael Sorter, Jonathan A. Bernstein
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Case Reports in Psychiatry
Online Access:http://dx.doi.org/10.1155/2018/8189067
id doaj-e1adc0543f7f4e05a7ec07ac62d24257
record_format Article
spelling 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
work_keys_str_mv AT drewhbarzman anatypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT hannahjackson anatypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT umeshsingh anatypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT marcusgriffey anatypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT michaelsorter anatypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT jonathanabernstein anatypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT drewhbarzman atypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT hannahjackson atypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT umeshsingh atypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT marcusgriffey atypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT michaelsorter atypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
AT jonathanabernstein atypicalpresentationofpediatricacuteneuropsychiatricsyndromerespondingtoplasmapheresistreatment
_version_ 1725776939916984320