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IgA and IgG/IgA intercellular dermatosis: a clinicopathological case series of 15 patients.

Authors :
Calmettes, V.
Badrignans, M.
Konstantinou, M.P.
Tancrède‐Bohin, E.
Vignon‐Pennamen, M.D.
Castel, M.
Pham‐Ledard, A.
Le Roux‐Villet, C.
Misery, L.
Schoenlaub, P.
Tronquoy, A.F.
Cordel, N.
Ortonne, N.
Sohier, P.
Cellier, L.
Tournier, E.
De La Salle, E.M.
Le Flahec, G.
Plantier, F.
Grootenboer‐Mignot, S.
Source :
Journal of the European Academy of Dermatology & Venereology; Nov2022, Vol. 36 Issue 11, pe896-e898, 3p
Publication Year :
2022

Abstract

Clinicopathologic features of IgG/IgA pemphigus in comparison with classic (IgG) and IgA pemphigus. Pemphigus with IgA deposits, called intercellular IgA dermatosis (IAD)1 or IgA pemphigus,2 is rare. Some cases are associated with anti-desmocollin antibodies.3 Intermediate IgG and IgA forms were reported, called intercellular IgG/IgA dermatosis (IGAD)4 or IgG/IgA pemphigus.5 We conducted a clinical pathological study to compare IAD and IGAD. [Extracted from the article]

Details

Language :
English
ISSN :
09269959
Volume :
36
Issue :
11
Database :
Complementary Index
Journal :
Journal of the European Academy of Dermatology & Venereology
Publication Type :
Academic Journal
Accession number :
159629916
Full Text :
https://doi.org/10.1111/jdv.18325