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European Journal of Dermatology

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Manifestations of cutaneous mycobacterial infections in patients with inborn errors of IL-12/IL-23-IFNγ immunity Volume 32, numéro 4, 2022-07-01

Illustrations


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Tableaux

Auteurs
1 Department of Paediatrics, First Faculty of Medicine, Charles University in Prague, Thomayer University Hospital, Prague, Czech Republic
2 National Institute of Child Tuberculosis and Respiratory Diseases, Dolny Smokovec, Slovakia
3 Department of Pathology and Molecular Medicine, Third Faculty of Medicine, Charles University in Prague, Thomayer University Hospital, Prague, Czech Republic
4 Centre for Cardiovascular Surgery and Transplantation, Brno, Czech Republic
5 Department of Immunology, Second Faculty of Medicine, Charles University in Prague, Motol University Hospital, Prague, Czech Republic
Reprints: Bloomfield Marketa

Background

Inborn errors of IL-12/IL-23-IFNγ immunity underlie Mendelian susceptibility to mycobacterial diseases (MSMD), a group of immunodeficiencies characterized by a highly selective susceptibility to weakly virulent strains of mycobacteria, such as non-tuberculous mycobacteria (NTM) and bacillus Calmette-Guérin (BCG). Cutaneous mycobacterial infections are common in MSMD and may represent a red flag for this immunodeficiency.

Objectives

We present a case series of four paediatric patients with MSMD, specifically with IFNγR1 and STAT1 deficiencies, and cutaneous NTM/BCG infections to increase awareness of this immunodeficiency, which may, in some cases, be intercepted by the dermatologist and thus timely referred to the immunologist.

Materials & Methods

Clinical, laboratory and genetic investigations of the four paediatric patients with MSMD are presented.

Results

All four presented patients experienced early complications after BCG vaccination. Two patients suffered recurrent mycobacteriosis, one patient experienced delayed BCG reactivation, and one patient died of disseminated avian mycobacteriosis. The dermatological manifestation in these patients included destructive nasal ulcerations, scrofuloderma of various sites and lupus vulgaris. All patients had a normal basic immune phenotype.

Conclusion

The presented cases demonstrate that NTM/BCG infections in otherwise seemingly immunocompetent patients should raise suspicion of MSMD. This is of utmost importance as specific therapeutic approaches, such as IFNγ treatment or haematopoietic stem cell transplantation, may be employed to improve the disease outcome.