Adult Kawasaki disease: a rare and challenging diagnosis—a case report

ABSTRACT: Abstract

Background

Kawasaki disease (KD) is an acute systemic vasculitis which predominantly occurs in childhood but rarely in adulthood. Diagnosis relies on the presence of typical clinical features; however, patients may present atypically, increasing the challenge of timely diagnosis for physicians.

Case summary

We report a case of a 40-year-old male presenting with persistent fever, rash, and unilateral neck swelling. Initial investigations were suggestive of necrotizing lymphadenitis, with a presumed infective aetiology. However, extensive microbiology and immunological investigations remained negative. Cardiac injury was evident with elevated troponin T and NT-proBNP; however, left ventricular systolic function was normal. After 4 days, clinical features consistent

SUBMITTER:  

PROVIDER: S-EPMC10482142 | biostudies-literature | 2023 Aug

REPOSITORIES: biostudies-literature