Literature DB >> 19262248

Rosai-Dorfman disease: a case with lymphadenopathy and liver involvement.

Anu Maheshwari1, Anju Seth, Monisha Choudhury, Varun Aggarwal, Bijoy Patra, Shilpi Aggarwal, Sharmila B Mukherjee, Satinder Aneja.   

Abstract

Rosai-Dorfman disease (RDD), originally described as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic proliferative disorder with a distinctive microscopic appearance. Formerly thought to be a disease process limited to lymph nodes, RDD has now been reported in many organ systems like bone, skin and soft tissue, central nervous system, eye and orbit, and upper respiratory tract. Here we report a case of RDD with hepatic involvement, which is even more rare.

Entities:  

Mesh:

Year:  2009        PMID: 19262248     DOI: 10.1097/MPH.0b013e31818e5369

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  2 in total

1.  Differential diagnosis in Rosai-Dorfman disease: A rare case of isolated hepatic presentation mimicking a metastatic tumor with positive 18-FDG uptake.

Authors:  Carlo Gazia; Luca Giordano; Maria Grazia Diodoro; Iacopo Compalati; Riccardo Avantifiori; Gian Luca Grazi
Journal:  Intractable Rare Dis Res       Date:  2022-05

Review 2.  Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature.

Authors:  Francesco di Dio; Ilaria Mariotti; Elena Coccolini; Patrizia Bruzzi; Barbara Predieri; Lorenzo Iughetti
Journal:  BMC Pediatr       Date:  2016-05-03       Impact factor: 2.125

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.