Osseous Localization of Rosai-Dorfman Disease

Overview

Journal J Hand Surg Br

Specialties Emergency Medicine
General Surgery

Date 1996 Jun 1

PMID 8771474

Citations 4

Authors

M N Rasool

P K Ramdial

Affiliations

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Abstract

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a disease of bone marrow stem cell origin which primarily affects lymph nodes. Solitary bone lesions are rare and can cause diagnostic difficulties. A primary lesion in the right index finger of a 10-month-old child is reported.

Citing Articles

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

Gupta A, Jindal A, Dey P, Gupta A Indian J Pediatr. 2017; 84(6):481-482.

PMID: 28205077 DOI: 10.1007/s12098-017-2299-z.

Extranodal Rosai-Dorfman disease: a rare soft tissue neoplasm masquerading as a sarcoma.

Komaragiri M, Sparber L, Santos-Zabala M, Dardik M, Chamberlain R World J Surg Oncol. 2013; 11:63.

PMID: 23497062 PMC: 3608083. DOI: 10.1186/1477-7819-11-63.

Multifocal osseous involvement as the sole manifestation of Rosai-Dorfman disease.

Sundaram C, Shantveer G, Chandrashekar P, Prasad V, Umadevi M Skeletal Radiol. 2005; 34(10):658-64.

PMID: 16094546 DOI: 10.1007/s00256-005-0951-6.

A solitary lesion of talus with mixed sclerotic and lytic changes: Rosai-Dorfman disease of 25 years' duration.

Abdelwahab I, Klein M, Springfield D, Hermann G Skeletal Radiol. 2004; 33(4):230-3.

PMID: 14740182 DOI: 10.1007/s00256-003-0681-6.