Literature DB >> 21557191

[Rosai -Dorfman disease: a two cases report].

Hadhami Ben Turkia1, Manal Ben Romdhane, Hatem Azzouz, Amel Ben Chehida, Mohamed Slim Abdelmoula, Rim Ben Abdelaziz, Neji Tebib, Monia Ben Messoud, Samia Sahtout, Ines Chelly, Moncef Zitouni, Emna Mnif, Marie Francoise Ben Dridi.   

Abstract

BACKGROUND: Rosai-Dorfman disease (RDD) is a benign lymphoproliferatif disorder characterized by cervical lymphadenopathies with a consistent risk of airways' compression and esthetical prejudice. Extra nodal localizations are also described. AIM: To report two pediatric cases of RDD. CASES: the first case concerned a patient with a prolonged nodal involvement of RDD. Remission seems to be natural although it coincided with a sulfaméthoxazole- triméthoprime therapy. The second case illustrated an extranodal form of RDD localized in soft tissue and paranasal sinus with extension to nasal cavity which were corticodependant.
CONCLUSION: RDD is usually a benign disorder. Particular localizations, lack of effective therapy and the high risk of recurrence are important issues in this rare affection.

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Year:  2011        PMID: 21557191

Source DB:  PubMed          Journal:  Tunis Med        ISSN: 0041-4131


  1 in total

1.  Long-term follow-up in two cases of intracranial Rosai-Dorfman Disease complicated by incomplete resection and recurrence.

Authors:  Diones Rivera; Miguelina Pérez-Castillo; Belkis Fernández; Peter Stoeter
Journal:  Surg Neurol Int       Date:  2014-02-28
  1 in total

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