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New onset ANCA-associated vasculitis in an adolescent during an acute COVID-19 infection: a case report.
Reiff, Daniel D; Meyer, Chloe G; Marlin, Brittany; Mannion, Melissa L.
  • Reiff DD; Children's of Alabama, Division of Rheumatology, Department of Pediatrics, University of Alabama at Birmingham, 1600 7th Ave. S., CPPN #G10, Birmingham, AL, 35233-1711, USA. danielreiff@uabmc.edu.
  • Meyer CG; UAB Pediatric Residency Program, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Marlin B; Division of Pediatric Hospital Medicine, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Mannion ML; Children's of Alabama, Division of Rheumatology, Department of Pediatrics, University of Alabama at Birmingham, 1600 7th Ave. S., CPPN #G10, Birmingham, AL, 35233-1711, USA.
BMC Pediatr ; 21(1): 333, 2021 08 05.
Article in English | MEDLINE | ID: covidwho-1344097
ABSTRACT

BACKGROUND:

SARS-CoV-2 has been found to be exquisitely adept at triggering autoimmunity and multiple new onset autoimmune diseases have been described as a post-infectious complication of COVID-19 infection in the adult population. Less has been described in the pediatric population, as infections are more likely to be asymptomatic and less severe. This case reports a previously healthy adolescent patient with new onset antineutrophil cytoplasmic autoantibody-associated vasculitis (AAV) diagnosed in the setting of acute COVID-19 infection. CASE PRESENTATION A previously healthy adolescent male was diagnosed with COVID-19 pneumonia after presenting with infectious symptoms of fever, cough, congestion, and shortness of breath. After worsening of disease, he was found to have pulmonary nodules, atypical for COVID-19. Further imaging and laboratory workup showed elevated inflammatory markers, negative infectious testing, and positive antineutrophil cytoplasmic antibodies (ANCA) diagnostic for AAV. He was treated with pulse dose steroids followed by a prolonged taper and rituximab. Symptoms resolved and laboratory abnormalities improved over time. At six-month follow-up, lesions were much improved, laboratory markers were within normal limits, and patient remained asymptomatic off medications.

CONCLUSIONS:

This case is one of the first in the pediatric population to describe new onset AAV presenting with an acute, symptomatic COVID-19 infection. There is increasing evidence for COVID-19 induced autoimmunity in the pediatric population and pediatric care providers should be on high alert for new onset autoimmune disease in children afflicted by COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis / COVID-19 / Infections Type of study: Case report / Cohort study / Diagnostic study / Prognostic study Topics: Long Covid Limits: Adolescent / Adult / Child / Humans / Male Language: English Journal: BMC Pediatr Journal subject: Pediatrics Year: 2021 Document Type: Article Affiliation country: S12887-021-02812-Y

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis / COVID-19 / Infections Type of study: Case report / Cohort study / Diagnostic study / Prognostic study Topics: Long Covid Limits: Adolescent / Adult / Child / Humans / Male Language: English Journal: BMC Pediatr Journal subject: Pediatrics Year: 2021 Document Type: Article Affiliation country: S12887-021-02812-Y