Chilblains in immune-mediated inflammatory diseases: a review

Author:

Dubey Shirish12ORCID,Joshi Nilay3,Stevenson Olivia3,Gordon Caroline4ORCID,Reynolds John A56ORCID

Affiliation:

1. Department of Rheumatology, Oxford University Hospitals NHS FT

2. Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford

3. Department of Rheumatology, Kettering general Hospital NHS FT , Kettering

4. Rheumatology Research Group—Institute of Inflammation and Ageing (IIA)

5. John A Reynolds Rheumatology Research Group, Institute of Inflammation and Ageing (IIA), University of Birmingham

6. Rheumatology Department, Sandwell and West Birmingham NHS Trust , Birmingham, UK

Abstract

AbstractChilblains were first described over a hundred years ago as cutaneous inflammatory lesions, typically on the digits, occurring on cold exposure. Chilblains can be primary, or secondary to a number of conditions such as infections, including COVID-19, and immune-mediated inflammatory disorders (IMIDs) with SLE being the commonest. Chilblain lupus erythematosus (CHLE) was first described in 1888 as cold-induced erythematous lesions before the terms ‘chilblains’ or ‘perniosis’ were coined. Diagnostic criteria exist for both chilblains and CHLE. Histopathologically, CHLE lesions show interface dermatitis with perivascular lymphocytic infiltrate. Immunofluorescence demonstrates linear deposits of immunoglobulins and complement in the dermo-epidermal junction. This narrative review focuses on chilblains secondary to immune-mediated inflammatory disorders, primarily the epidemiology, pathogenesis and treatment of CHLE.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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