Extranodal sinonasal rosai-dorfman disease in a Nigerian woman: A case report and review of literature

A. Ajiya, E. Kolo, I. Shuaibu
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Abstract

Rosai Dorfman disease (RDD) also referred to as sinus histiocytosis with massive lymphadenopathy is a rare non-neoplastic lymphoproliferative disease with unknown etiology and pathogenesis first described by Rosai and Dorfman in 1969. It is characterized by histiocytic proliferation of lymphatic sinuses, which primarily involves the lymph nodes, but has an extranodal tendency. Frequently encountered extranodal sites in the head-and-neck region is paranasal sinuses and nasal cavity, orbit, parotid gland, and middle ear. We present a case of RDD occurring in the nasal cavity of a 28-year-old female from Nigeria. RDD should be considered a differential diagnosis in any patient with benign sinonasal mass especially arising from the nasal septum with massive cervical lymphadenopathy.
结外鼻窦玫瑰-多夫曼病1例尼日利亚妇女:1例报告及文献复习
Rosai Dorfman病(Rosai Dorfman disease, RDD)又称窦性组织细胞增生伴大量淋巴结病,是一种罕见的非肿瘤性淋巴增生性疾病,病因和发病机制尚不清楚,由Rosai和Dorfman于1969年首次报道。其特点是淋巴窦的组织细胞增生,主要累及淋巴结,但有结外倾向。头颈部结外最常见的部位是鼻窦、鼻腔、眼眶、腮腺和中耳。我们提出一个病例的RDD发生在鼻腔的一个28岁的女性从尼日利亚。对于任何有良性鼻窦肿块的患者,尤其是起源于鼻中隔并伴有大量颈部淋巴结病的患者,RDD应被视为鉴别诊断。
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