Rosai-Dorfman disease associated with neurosensorial hearing loss in two siblings.

Abstract:

:Rosai-Dorfman disease (RDD) is an uncommon pathologic condition of unknown ethiology with an idiopathic proliferation of the hystiocytes. It is generally presented with massive bilateral hypertrophy of the cervical lymph nodes. But other lymph nodes may also be involved. Approximately, 30% of these patients have extra nodal mass or lesion with different signs or symptoms depending on localization. We present two male siblings with Rosai-Dorfman disease who have classical cervical lymphadenopathy associated with progressive neurosensorial hearing loss and dural-based intracranial lesions.

authors

Yetiser S,Cekin E,Tosun F,Yildirim A

doi

10.1016/j.ijporl.2004.03.014

subject

Has Abstract

pub_date

2004-08-01 00:00:00

pages

1095-100

issue

8

eissn

0165-5876

issn

1872-8464

pii

S0165587604001041

journal_volume

68

pub_type

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