Pediatr Dermatol. 2024 Jun 17. doi: 10.1111/pde.15670. Online ahead of print.
ABSTRACT
An otherwise healthy 4-week-old term female of Japanese heritage presented with a 1-week history of asymptomatic progressive, generalized skin lesions. The lesion morphology, distribution, and dermatopathology result was consistent with Sweet syndrome. The patient was found to have a congenital type H rectovestibular fistula. This case highlights the rare association of rectovestibular fistula in neonatal Sweet syndrome which has only been described in neonates of Japanese heritage.
PMID:38886158 | DOI:10.1111/pde.15670