تقرير
مرض روزاي-دورفمان المعزول في الأنسجة الرخوة تقرير حالة = Soft Tissue Rosai-Dorfman Disease Case report

Rajib, Rubyath C.


 

مرض روزاي-دورفمان المعزول في الأنسجة الرخوة تقرير حالة = Soft Tissue Rosai-Dorfman Disease Case report

Rajib, Rubyath C.

Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by massive lymphadenopathy. While extranodal involvement can occur in generalised RDD, isolated soft tissue RDD (STRDD) is extremely rare. We report a 17-year-old male patient who presented to the maxillofacial outpatient department of the Sultan Qaboos Hospital, Salalah, Oman, in 2015 with a painless cheek mass which had been slowly growing over the previous two months. Routine histopathological examinations and immunohistochemistry confirmed a diagnosis of STRDD. Currently, surgical excision is considered to be the most effective curative treatment for STRDD, as the outcomes of other treatment modalities are still unknown. Despite its rarity, STRDD should be considered in the differential diagnosis of histiocytic soft tissue lesions.

Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by massive lymphadenopathy. While extranodal involvement can occur in generalised RDD, isolated soft tissue RDD (STRDD) is extremely rare. We report a 17-year-old male patient who presented to the maxillo...

مادة فرعية

المؤلف : Rajib, Rubyath C.

مؤلف مشارك : Rajasekharan Pillai
Ibrahim A. Sulaiman
Al Haddabi, Ibrahim

بيانات النشر : Muscat، Sultanate of Oman : Sultan Qaboos University / College of Medicine and Health Sciences، 2017مـ.

التصنيف الموضوعي : العلوم التطبيقية|العلوم الطبية .

المواضيع : Rosai-Dorfman disease .

مرض روزاي-دورفمان .

رقم الطبعة : 4

المصدر : Sultan Qaboos University / College of Medicine and Health Sciences : Muscat، Sulatante of Oman.

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