The systemic autoinflammatory disorders for dermatologists. Part 1: overview.


Journal

Clinical and experimental dermatology
ISSN: 1365-2230
Titre abrégé: Clin Exp Dermatol
Pays: England
ID NLM: 7606847

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 09 03 2020
accepted: 11 03 2020
pubmed: 10 9 2020
medline: 29 7 2021
entrez: 9 9 2020
Statut: ppublish

Résumé

The systemic autoinflammatory disorders (SAIDs) or periodic fever syndromes are disorders of innate immunity, which can be inherited or acquired. They are almost all very rare and easily overlooked; typically, patients will have seen multiple specialities prior to diagnosis, so a high level of clinical suspicion is key. It is important to note that these are 'high-value' diagnoses as the majority of these syndromes can be very effectively controlled, dramatically improving quality of life and providing protection against the development of irreversible complications such as AA amyloidosis. In this article, we take an overview of SAIDs and look at the common features; in Part 2, we take a more in-depth look at the better recognized or more dermatologically relevant conditions.

Identifiants

pubmed: 32901977
doi: 10.1111/ced.14250
doi:

Substances chimiques

Interleukin-1beta 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

962-966

Informations de copyright

© 2020 The Authors. Clinical and Experimental Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.

Références

Hausmann JS, Lomax KG, Shapiro A, Durrant K. The patient journey to diagnosis and treatment of autoinflammatory diseases. Orphanet J Rare Dis 2018; 13: 156.
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McDermott MF, Aksentijevich I, Galon J et al. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 1999; 97: 133-44.
Simon A, Asli B, Braun-Falco M et al. Schnitzler's syndrome: diagnosis, treatment, and follow-up. Allergy 2013; 68: 562-8.
Kallinich T, Gattorno M, Grattan CE et al. Unexplained recurrent fever: when is autoinflammation the explanation? Allergy 2013; 68: 285-96.
Hutchinson M, Tattersall RS, Manson JJ. Haemophagocytic lymphohisticytosis-an underrecognized hyperinflammatory syndrome. Rheumatology (Oxford) 2019; 58: vi23-30.
Barzilai A, Langevitz P, Goldberg I et al. Erysipelas-like erythema of familial Mediterranean fever: clinicopathologic correlation. J Am Acad Dermatol 2000; 42: 791-5.
Broekaert SMC, Böer-Auer A, Kerl K et al. Neutrophilic epitheliotropism is a histopathological clue to neutrophilic urticarial dermatosis. Am J Dermatopathol 2016; 38: 39-49.
Fanoni D, Venegoni L, Vergani B et al. Evidence for a role of autoinflammation in early-phase psoriasis. Clin Exp Immunol 2019; 198: 283-91.

Auteurs

J Oldham (J)

Portsmouth Hospitals NHS Trust, National Amyloidosis Centre, UCL Division of Medicine and Royal Free London NHS Foundation Trust, Portsmouth, Hampshire, UK.

H J Lachmann (HJ)

Portsmouth Hospitals NHS Trust, National Amyloidosis Centre, UCL Division of Medicine and Royal Free London NHS Foundation Trust, Portsmouth, Hampshire, UK.

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