Rosai-Dorfman Disease of the Nasal Cavity and Nasopharynx.
- Author:
Hyung Kwon BYEON
1
;
Yoo Suk KIM
;
Junjeong CHOI
;
Joo Heon YOON
Author Information
1. Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Korea. hyoon@yuhs.ac
- Publication Type:Case Report
- Keywords:
Rosai-Dorfman disease;
Nasal cavity;
Nasopharynx
- MeSH:
Adult;
Biopsy;
Cytoplasm;
Endoscopy;
Head;
Histiocytes;
Histiocytosis, Sinus;
Humans;
Lymphatic Diseases;
Lymphocytes;
Male;
Nasal Cavity;
Nasal Obstruction;
Nasopharynx;
Neck;
Plasma Cells
- From:Korean Journal of Otolaryngology - Head and Neck Surgery
2008;51(6):570-573
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Rosai-Dorfman disease is a rare disorder of unknown etiology and is usually associated with benign proliferation of hematopoietic and fibrous tissue that often manifests in the head and neck region. The most common clinical presentation of this entity is bilateral, nontender cervical lymphadenopathy, but an extranodal form of the disease may develop in up to 43% of patients. We report a case of extranodal Rosai-Dorfman disease occurring in the nasal cavity and the nasopharynx. A 25-year-old male visited the clinic with a complaint of nasal obstruction for several months. Mass originating from anterior portion of septum and nasopharyngeal cavity was observed by endoscopy. Endoscopic guided incisional biopsy of the lesion was performed. The histopathologic findings revealed clusters of large, foamy histiocytes with abundant clear cytoplasm, lymphophagocytosis, and heavy infiltration of lymphocytes and plasma cells, which are the key features of Rosai-Dorfman disease.
