Towards a better understanding of adult idiopathic epidermal necrolysis: a retrospective study of 19 cases

Author:

Monnet P.1ORCID,Rodriguez C.234,Gaudin O.14,Cirotteau P.5,Papouin B.6,Dereure O.47ORCID,Tetart F.48,Lalevee S.19ORCID,Colin A.14,Lebrun‐Vignes B.410,Abe E.11,Alvarez J.‐C.11,Demontant V.23,Gricourt G.23,de Prost N.41213,Barau C.14,Chosidow O.1413,Wolkenstein P.1413,Hue S.4913,Ortonne N.4613ORCID,Milpied B.45ORCID,Ingen‐Housz‐Oro S.1415ORCID

Affiliation:

1. Dermatology Department AP‐HP Henri Mondor Hospital Créteil France

2. Microbiology Department AP‐HP Henri Mondor Hospital Créteil France

3. INSERM U955 Université Paris Est Créteil Val de Marne UPEC Créteil France

4. Reference Center for Toxic Bullous Diseases and Severe Drug Reactions TOXIBUL Créteil France

5. Dermatology Department Saint André Hospital Bordeaux France

6. Pathology Department AP‐HP Henri Mondor Hospital Créteil France

7. Dermatology Department Saint Eloi Hospital Montpellier France

8. Dermatology Department Charles Nicole Hospital Rouen France

9. Immunology Department INSERM Unité U955 Institut Mondor de Recherche Biomédicale AP‐HP Henri Mondor Hospital Créteil France

10. Pharmacovigilance Department AP‐HP Pitié‐Salpêtrière Hospital Paris France

11. Pharmacology and Toxicology Department AP‐HP Raymond Poincaré Hospital Garches France

12. Intensive Care Unit AP‐HP Henri Mondor Hospital Créteil France

13. Université Paris Est Créteil Val de Marne UPEC Créteil France

14. Clinical Investigation Center Henri Mondor Hospital Créteil France

15. Univ Paris Est Créteil EpidermE Créteil France

Abstract

AbstractBackgroundMost cases of Stevens–Johnson syndrome and toxic epidermal necrolysis are drug‐induced. A small subset of cases remain with unknown aetiology (idiopathic epidermal necrolysis [IEN]).ObjectiveWe sought to better describe adult IEN and understand the aetiology.MethodsThis retrospective study was conducted in 4 centres of the French national reference centre for epidermal necrolysis. Clinical data were collected for the 19 adults hospitalized for IEN between January 2015 and December 2019. Wide toxicology analysis of blood samples was performed. Histology of IEN cases was compared with blinding to skin biopsies of drug‐induced EN (DIEN, ‘controls’). Available baseline skin biopsies were analysed by shotgun metagenomics and transcriptomics and compared to controls.ResultsIEN cases represented 15.6% of all EN cases in these centres. The median age of patients was 38 (range 16–51) years; 68.4% were women. Overall, 63.2% (n = 12) of cases required intensive care unit admission and 15.8% (n = 3) died at the acute phase. Histology showed the same patterns of early‐ to late‐stage EN with no difference between DIEN and IEN cases. One toxicology analysis showed unexpected traces of carbamazepine; results for other cases were negative. Metagenomics analysis revealed no unexpected pathological microorganism. Transcriptomic analysis highlighted a different pro‐apoptotic pathway in IEN compared to DIEN, with an overexpression of apoptosis effectors TWEAK/TRAIL.ConclusionsIEN affects young people and is a severe form of EN. A large toxicologic investigation is warranted. Different pathways seem involved in IEN and DIEN, leading to the same apoptotic effect, but the primary trigger remains unknown.

Publisher

Wiley

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