Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome
Background: With the advent of more sensitive culture and molecular diagnostic testing modalities, Bartonella spp. infections have been documented in blood and/or cerebrospinal fluid specimens from patients with diverse neurological symptoms. Pediatric acute-onset neuropsychiatric syndrome (PANS) is...
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Online Access: | https://doi.org/10.1177/1179573519832014 |
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doaj-af8f8984cc7b4b419052a0237d8602b32020-11-25T03:24:38ZengSAGE PublishingJournal of Central Nervous System Disease1179-57352019-03-011110.1177/1179573519832014 Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric SyndromeEdward B Breitschwerdt0Rosalie Greenberg1Ricardo G Maggi2B Robert Mozayeni3Allen Lewis4Julie M Bradley5Intracellular Pathogens Research Laboratory, Comparative Medicine Institute, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USAMedical Arts Psychotherapy Associates P.A., Summit, NJ, USAIntracellular Pathogens Research Laboratory, Comparative Medicine Institute, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USATranslational Medicine Group PC, North Bethesda, MD, USASancta Familia Center for Integrative Medicine, Columbus, OH, USAIntracellular Pathogens Research Laboratory, Comparative Medicine Institute, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USABackground: With the advent of more sensitive culture and molecular diagnostic testing modalities, Bartonella spp. infections have been documented in blood and/or cerebrospinal fluid specimens from patients with diverse neurological symptoms. Pediatric acute-onset neuropsychiatric syndrome (PANS) is characterized by an unusually abrupt onset of cognitive, behavioral, or neurological symptoms. Between October 2015 and January 2017, a 14-year-old boy underwent evaluation by multiple specialists for sudden-onset psychotic behavior (hallucinations, delusions, suicidal and homicidal ideation). Methods: In March 2017, Bartonella spp. serology (indirect fluorescent antibody assays) and polymerase chain reaction (PCR) amplification, DNA sequencing, and Bartonella enrichment blood culture were used on a research basis to assess Bartonella spp. exposure and bloodstream infection, respectively. PCR assays targeting other vector-borne infections were performed to assess potential co-infections. Results: For 18 months, the boy remained psychotic despite 4 hospitalizations, therapeutic trials involving multiple psychiatric medication combinations, and immunosuppressive treatment for autoimmune encephalitis. Neurobartonellosis was diagnosed after cutaneous lesions developed. Subsequently, despite nearly 2 consecutive months of doxycycline administration, Bartonella henselae DNA was PCR amplified and sequenced from the patient’s blood, and from Bartonella alphaproteobacteria growth medium enrichment blood cultures. B henselae serology was negative. During treatment with combination antimicrobial chemotherapy, he experienced a gradual progressive decrease in neuropsychiatric symptoms, cessation of psychiatric drugs, resolution of Bartonella -associated cutaneous lesions, and a return to all pre-illness activities. Conclusions: This case report suggests that B henselae bloodstream infection may contribute to progressive, recalcitrant neuropsychiatric symptoms consistent with PANS in a subset of patients.https://doi.org/10.1177/1179573519832014 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Edward B Breitschwerdt Rosalie Greenberg Ricardo G Maggi B Robert Mozayeni Allen Lewis Julie M Bradley |
spellingShingle |
Edward B Breitschwerdt Rosalie Greenberg Ricardo G Maggi B Robert Mozayeni Allen Lewis Julie M Bradley Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome Journal of Central Nervous System Disease |
author_facet |
Edward B Breitschwerdt Rosalie Greenberg Ricardo G Maggi B Robert Mozayeni Allen Lewis Julie M Bradley |
author_sort |
Edward B Breitschwerdt |
title |
Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome |
title_short |
Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome |
title_full |
Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome |
title_fullStr |
Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome |
title_full_unstemmed |
Bloodstream Infection in a Boy With Pediatric Acute-Onset Neuropsychiatric Syndrome |
title_sort |
bloodstream infection in a boy with pediatric acute-onset neuropsychiatric syndrome |
publisher |
SAGE Publishing |
series |
Journal of Central Nervous System Disease |
issn |
1179-5735 |
publishDate |
2019-03-01 |
description |
Background: With the advent of more sensitive culture and molecular diagnostic testing modalities, Bartonella spp. infections have been documented in blood and/or cerebrospinal fluid specimens from patients with diverse neurological symptoms. Pediatric acute-onset neuropsychiatric syndrome (PANS) is characterized by an unusually abrupt onset of cognitive, behavioral, or neurological symptoms. Between October 2015 and January 2017, a 14-year-old boy underwent evaluation by multiple specialists for sudden-onset psychotic behavior (hallucinations, delusions, suicidal and homicidal ideation). Methods: In March 2017, Bartonella spp. serology (indirect fluorescent antibody assays) and polymerase chain reaction (PCR) amplification, DNA sequencing, and Bartonella enrichment blood culture were used on a research basis to assess Bartonella spp. exposure and bloodstream infection, respectively. PCR assays targeting other vector-borne infections were performed to assess potential co-infections. Results: For 18 months, the boy remained psychotic despite 4 hospitalizations, therapeutic trials involving multiple psychiatric medication combinations, and immunosuppressive treatment for autoimmune encephalitis. Neurobartonellosis was diagnosed after cutaneous lesions developed. Subsequently, despite nearly 2 consecutive months of doxycycline administration, Bartonella henselae DNA was PCR amplified and sequenced from the patient’s blood, and from Bartonella alphaproteobacteria growth medium enrichment blood cultures. B henselae serology was negative. During treatment with combination antimicrobial chemotherapy, he experienced a gradual progressive decrease in neuropsychiatric symptoms, cessation of psychiatric drugs, resolution of Bartonella -associated cutaneous lesions, and a return to all pre-illness activities. Conclusions: This case report suggests that B henselae bloodstream infection may contribute to progressive, recalcitrant neuropsychiatric symptoms consistent with PANS in a subset of patients. |
url |
https://doi.org/10.1177/1179573519832014 |
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