Literature DB >> 19061211

Congenital Rosai-Dorfman disease presenting with anemia, thrombocytopenia, and hepatomegaly.

C P Chow1, H K Ho, G C F Chan, A N Cheung, S Y Ha.   

Abstract

Rosai-Dorfman disease (RDD) is a rare entity of non-Langerhans cell histiocytoses (non-LCH) which usually presents with bilateral painless cervical lymphadenopathy. We describe a neonate with RDD who presented with anemia, thrombocytopenia and hepatomegaly. He recovered spontaneously with conservative management. This represents an atypical presentation of RDD. Conservative management with close monitoring can be adopted for some with systemic involvement.

Entities:  

Mesh:

Year:  2009        PMID: 19061211     DOI: 10.1002/pbc.21880

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

1.  Rosai Dorfman Disease in an Infant: An Unusual Cause of Cervical Lymphadenopathy.

Authors:  Aman Gupta; Ankur Kumar Jindal; Pranab Dey; Anju Gupta
Journal:  Indian J Pediatr       Date:  2017-02-16       Impact factor: 1.967

2.  Rosai-Dorfman Disease with nodal and extranodal involvements: A case report.

Authors:  Mehri Najafi-Sani; Hossein Saneian; Fatemeh Mahjoub
Journal:  J Res Med Sci       Date:  2011-09       Impact factor: 1.852

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.