[Adult Kawasaki disease: A diagnostic case report].
Ann Pathol 2026 May; 46(3):275-279.

Abstract

Kawasaki disease (KD) is an acute systemic vasculitis mainly affecting medium-size blood vessels and primarily affecting children under five years old. The typical clinical presentation associates fever, skin rash, mucous membrane abnormalities, and lymphadenopathies. Occurrence in adults is rare, with fewer than 100 cases reported and limited histological descriptions available, particularly regarding the skin. We report herein the case of a 22-year-old man hospitalized for fever, odynophagia, and aphagia since five days. Clinical examination revealed enanthem with palatal ulcerations, maculopapular lesions with fine scaling on the limbs and extremities, painful scrotal ulcerations, bilateral non-exudative conjunctivitis, and bilateral lymphadenopathy. Laboratory tests showed an isolated inflammatory syndrome. Skin biopsy revealed lichenoid epidermal changes along with a polymorphic dermal inflammatory infiltrate exhibiting a granulomatous pattern and comprising abundant lymphocytes, accompanied by vascular changes. The diagnosis of KD was established by integrating clinical and histological data. Early recognition of this disease in adults is essential to prevent chronic complications; this report aims to describe its potential histological features.

Authors+Show Affiliations

Leclerc VInstitut de pathologie multisites, hospices civils de lyon, hôpital Lyon Sud, Lyon, France. Electronic address: valentine.leclerc@chu-lyon.fr.
Danset MService de dermatologie, hospices civils de lyon, groupement hospitalier Nord, Lyon, France.
Durupt FService de dermatologie, hospices civils de lyon, groupement hospitalier Nord, Lyon, France.
Berset-de-Vaufleury JService de dermatologie, hospices civils de lyon, groupement hospitalier Nord, Lyon, France.
Tabary AService de médecine interne, hospices civils de lyon, groupement hospitalier Nord, Lyon, France.
Tantot JInstitut de pathologie multisites, hospices civils de lyon, hôpital Lyon Sud, Lyon, France.
Trecourt AInstitut de pathologie multisites, hospices civils de lyon, hôpital Lyon Sud, Lyon, France; UFR médecine Lyon Sud, université Lyon 1, 69921 Lyon, France; Centre pour l'innovation en cancérologie de Lyon (CICLY), UR3738, UFR médecine Lyon Sud, UCBL1, Oullins-Pierre-Bénite, France.
Harou OInstitut de pathologie multisites, hospices civils de lyon, hôpital Lyon Sud, Lyon, France.
Balme BInstitut de pathologie multisites, hospices civils de lyon, hôpital Lyon Sud, Lyon, France.
Donzel MInstitut de pathologie multisites, hospices civils de lyon, hôpital Lyon Sud, Lyon, France; UFR médecine Lyon Sud, université Lyon 1, 69921 Lyon, France; UMR5308, Institut national de la santé et de la recherche médicale (Inserm) U1111, Centre international de recherche en infectiologie (CIRI), UFR Lyon-1, Centre national de la recherche scientifique (CNRS), École normale supérieure de Lyon, Lyon, France.

Pub Type(s)

Journal Article
Case Reports
English Abstract

Language

fre

PubMed ID

41605769