Rosai‐Dorfman disease presenting with nasal, nodal and multiple cutaneous involvements responding to a combination of systemic steroid and low‐dose thalidomide therapy
Abstract
The data that support the findings of this study are available from the corresponding author upon reasonable request. FIGURE S1: A,B, Histopathological examination of the skin lesions revealed dermal nodules consisting of numerous large histiocytes, lymphocytes, plasma cells and neutrophils (Hematoxylin & Eosin [H&E], ×2.8, ×15.8); (C) Emperipolesis characterized by the presence of neutrophils, lymphocytes, and plasma cells in the cytoplasm of histiocytes (H&E, ×60); (D,E) the histiocytes were diffusely CD68 and S-100-positive at immunohistochemical analysis (CD68, ×7 and S-100, ×18.8) Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Related Papers
- → Extranodal Rosai–Dorfman Disease Arising in the Right Atrium(2011)13 cited
- → Polypoid intranasal mass caused by Rosai–Dorfman disease: a diagnostic pitfall(2009)9 cited
- → Cutaneous rosai dorfman disease: A case report and literature review(2016)5 cited
- → Central nervous system involvement in Rosai‐Dorfman disease: Report of a case with a review of the literature(1999)5 cited
- → A case of Rosai-Dorfman disease with typical cytological feature(2008)