Mediastinal Rosai-Dorfman Disease with KRAS mutation case report and literature review

Abstract Background Rosai-Dorfman Disease (RDD) is a rare self-limiting histiocytosis, more prevalent in children and young adults. It typically manifests as painless bilateral massive cervical lymphadenopathy but may also extend to extra-nodal sites, with intrathoracic RDD noted in 2% of cases. Dis...

Full description

Bibliographic Details
Main Authors: Wenyu Zhang, Linan Fang, Jing Wang, Xiaobo Ma, Xintong Hu, Wei Liu
Format: Article
Language:English
Published: BMC 2024-04-01
Series:Journal of Cardiothoracic Surgery
Subjects:
Online Access:https://doi.org/10.1186/s13019-024-02668-0