Disseminated Mycobacterial Infection With Reactive Polyarthritis (Poncet’s Disease) During Immune-suppressive Treatment Including Ustekinumab for Pediatric Crohn’s Disease

Author:

Minotti Chiara12ORCID,Costenaro Paola1,Donà Daniele1,Zuliani Monica3,Bosa Luca4,Leon Alberta5,Perilongo Giorgio6,Gaio Paola4,Martini Giorgia7,Cananzi Mara4

Affiliation:

1. From the Division of Pediatric Infectious Diseases, Department of Women’s and Children’s Health, University of Padova, Padova, Italy

2. PhD Program in Clinical Research, Pediatric Research Center, University Children’s Hospital Basel, Basel, Switzerland

3. Pediatric Radiology, Department for Integrated Diagnostic Services

4. Pediatric Gastroenterology, Digestive Endoscopy, Hepatology and Care of the Child with Liver Transplantation, Department of Women’s and Children’s Health, University Hospital of Padova

5. Research & Innovation (R&I Genetics) Srl

6. Department of Women’s and Children’s Health, University of Padova

7. Pediatric Rheumatology, Department of Women’s and Children’s Health, University Hospital of Padova, Padova, Italy.

Abstract

Background: The incidence of pediatric inflammatory bowel disease is increasing. tumor necrosis factor alpha inhibitors medicines improved the prognosis of affected subjects. Nonetheless, a proportion of patients do not respond or lose response to treatment. Newer biologics, like ustekinumab, have been approved for adults. The pediatric off-label use of these drugs is increasing, despite limited safety evidence. We report a case of disseminated mycobacterial infection (MI) presenting with reactive polyarthritis (Poncet’s disease, PD) in a girl with Crohn’s disease receiving various immunosuppressants, including ustekinumab. Case Report: A 12-year-old girl with Crohn’s disease was admitted for acute-onset migratory polyarthritis of large and small joints and opioid-resistant pain. She had recently received adalimumab and methotrexate and was currently under treatment with ustekinumab. She was vaccinated with Bacillus Calmette-Guérin and screened for tuberculosis before starting immunosuppressants. Interferon-gamma release assay, Mantoux test and chest computed tomography scan were negative. Disseminated MI with PD was diagnosed following positive cultures for Mycobacterium tuberculosis complex in blood and intestinal biopsies (with negative in synovial fluid and gastric aspirate). Whole-exome sequencing did not identify any genetic susceptibility to MI. Antituberculosis treatment eradicated MI. Conclusions: Children with inflammatory bowel disease receiving combination immunosuppressive treatments including tumor necrosis factor alpha inhibitors and anti-IL-12/23 agents are at higher risk for MI. Disseminated MI should be considered and ruled out in these patients when presenting with pulmonary, extrapulmonary or unusual clinical manifestations, like PD. The collection of multiple specimens (including intestinal biopsies) for mycobacterial culture is recommended when mycobacterial disease is suspected.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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1. Multiple drugs;Reactions Weekly;2024-04-27

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