4.6 Article

Paediatric Inflammatory Multisystem Syndrome Temporally Associated With SARS-CoV-2 [PIMS-TS] in a Patient Receiving Infliximab Therapy for Inflammatory Bowel Disease

Journal

JOURNAL OF CROHNS & COLITIS
Volume 15, Issue 4, Pages 687-691

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ecco-jcc/jjaa201

Keywords

Paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 [PIMS-TS]; SARS-CoV-2; paediatric; inflammatory bowel disease

Funding

  1. Edinburgh Children's Hospital Charity-Catherine McEwan Foundation Research Fellowship
  2. Ferring
  3. Predictimmune

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PIMS-TS is a newly described pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. The patient in this case study showed improvement after treatment with high-dose methylprednisolone.
Paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 [PIMS-TS] is a newly described condition. It has a spectrum of presentations proposed to occur as part of a post-infectious immune response. We report the first case of PIMS-TS in a child on established anti-tumour necrosis factor alpha [anti-TNF alpha] therapy; a 10 year-old girl with ulcerative colitis treated with infliximab. The patient had 6 weeks of daily fever with mucocutaneous, gastrointestinal, renal, and haematological involvement. Biomarkers of hyperinflammation were present including: hyperferritinaemia [up to 691 mu/L; normal 15-80 mu g/L], C-reactive protein [CRP] [>100mg/L for >10 days, normal 0-5 mg/L], erythrocyte sedimentation rate [ESR] consistently >100mm/h [normal 0-15 mm/h], raised white cell count with neutrophilia, elevated D-dimer and lactate dehydrogenase [LDH], anaemia and Mott cells on bone marrow analysis. Extensive investigations for alternative diagnoses for pyrexia of unknown origin [PUO] were negative. The condition was refractory to treatment with intravenous immunoglobulin [IVIG] but improved within 24 h of high-dose methylprednisolone. Infliximab treatment followed and the patient has remained well at follow-up. Polymerase chain reaction [PCR] and serology for SARS-CoV-2 were negative. Current series report such negative findings in up to half of cases. The patient experienced a milder clinical phenotype without cardiac involvement, shock, or organ failure. Accepting the wide spectrum of PIMS-TS presentations, it is possible that previous anti-TNF alpha therapy may have attenuated the disease course. Given the uncertainty around therapeutic strategies for PIMS-TS, this case supports the need for further investigation into continuing infliximab as a treatment option for the condition.

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