Back to Search Start Over

Intraoral Lymphomatoid Papulosis Type D Showing Scarce/Absent CD30 Expression in A Pediatric Patient: Case Report and Literature Review.

Authors :
Palaçon, Mariana Paravani
Marques, Marcelo Borges
Silveira, Débora Fernandes Mendes
Martins, Karina Helen
Silveira, Heitor Albergoni
Pereira-Filho, Valfrido Antonio
Bufalino, Andreia
Chahud, Fernando
León, Jorge Esquiche
Source :
Head & Neck Pathology; 2/5/2025, Vol. 19 Issue 1, p1-5, 5p
Publication Year :
2025

Abstract

Purpose: Approximately 10% of all lymphomatoid papulosis (LyP) cases affect pediatric patients. Pediatric LyP is clinically similar to adult LyP, frequently with cutaneous involvement, whereas the affectation of mucosal surface is rare. The LyP clinicopathological spectrum includes type A, B, C, D, E, and LyP with DUSP22/IRF4 rearrangement, with LyP type D representing < 5% of all LyP cases. Methods: We have previously reported 2 cases of exclusively intraoral LyP type C and E. To date, about 50 cases of LyP type D have been reported; of them, 8 cases, all but one with exclusive skin involvement, corresponded to pediatric patients. Rare LyP type C cases can lack CD30 expression, creating diagnostic difficulties with lymphoma. Results: Here, we report an extremely rare case of intraoral LyP type D with scarce/absent CD30 expression affecting a 12-year-old white Brazilian boy. Conclusions: To our best knowledge, this is the first pediatric case of LyP type D with exclusive intraoral involvement. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1936055X
Volume :
19
Issue :
1
Database :
Complementary Index
Journal :
Head & Neck Pathology
Publication Type :
Academic Journal
Accession number :
182844054
Full Text :
https://doi.org/10.1007/s12105-024-01749-9