Pediatric orbital Rosai-Dorfman disease: An unusual case

CONCLUSION: Rosai-Dorfman disease is very rare in its bilateral orbital presentation. Histopathological diagnosis remains challenging. In Africa, the presence of chronic oculo-palpebral tumor associated with or without cervical lymphadenopathy must raise the suspicion of Rosai-Dorfman disease after ruling out tuberculosis and lymphoma.PMID:38310692 | DOI:10.1016/j.jfo.2024.104070

Source: Journal Francais d Ophtalmologie - February 4, 2024 Category: Opthalmology Authors: B Wade C A Lame M N Ndiaye Sow A Ndiaye F Di édhiou M Diakhat é E L H S Sarr S M Seck A D Faye N N Gueye Source Type: research