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Unusual Presentation of Rosai-Dorfman Disease (RDD) in the Bone in Adolescents

Authors :
Carlos R. Abramowsky
Mark L. Wulkan
Justine S. Broecker
Sarah Catherine Shulman
Bahig M. Shehata
Howard M. Katzenstein
Source :
Fetal and Pediatric Pathology. 30:442-447
Publication Year :
2011
Publisher :
Informa UK Limited, 2011.

Abstract

Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy (SHML), is a rare idiopathic histiocytic disorder. The usual presentation of RDD is painless bilateral cervical lymphadenopathy. Extranodal RDD with lymphadenopathy occurs in almost 50% of patients but extranodal RDD, without lymphadenopathy, is very rare. Isolated RDD in the bone occurs in only 2% of patients but it is histologically similar to its nodal counterpart. There are only 14 previously reported cases of RDD in the bone without lymph node involvement in children. Here we describe two new patients--one with rib and lung involvement and the other with multi-osseous involvement.

Details

ISSN :
15513823 and 15513815
Volume :
30
Database :
OpenAIRE
Journal :
Fetal and Pediatric Pathology
Accession number :
edsair.doi.dedup.....fb8b9dcc5e67a0d5af9d20ae9833d89c
Full Text :
https://doi.org/10.3109/15513815.2011.618873