B. M. Wenig and D. K. Heffner, “Respiratory Epithelial Adenomatoid Hamartomas of the Sinonasal Tract and Nasopharynx: A Clinicopathologic Study of 31 Cases,” Annals of Otology, Rhinology and Laryngology, Vol. 104, No. 8, 1995, pp. 639-645.

has been cited by the following article:

• TITLE: Tumor Misdiagnosed As Cancer of the Sphenoid Sinus: Case Report and Literature Review

  AUTHORS: El Fatemi Hinde, Bennani Amal, Souaf Ihsane, Zaki Zouhir, Alami Noureddine, Amarti Afaf

  KEYWORDS: Nasal Cavity; REAH; Nasal Polyposis; Hamartoma; Nasal Obstruction

  JOURNAL NAME: International Journal of Otolaryngology and Head & Neck Surgery, Vol.1 No.2, August 20, 2012

  ABSTRACT: Respiratory epithelial adenomatoid hamartoma (REAH) is an uncommon lesion of the upper aerodigestive tract first described by Wenig and Heffner in 1995 as prominent glandular proliferations lined by ciliated respiratory epithelium originating from the surface epithelium. Case Report: We report a case of 48-year-old women with nasal polyposis history, which consults for nasal obstruction, with suspicion of malignancy on CT. Surgical resection showed a respiratory epithelial adenomatoid hamartoma (REAH) of the nasal cavity. Conclusion: REAH is a recently described pathologic entity that can present rhinorrhea, epistaxis, hyposmia, and headaches. It is a rare lesion of nasal and paranasal sinuses, but should be considered in the differential diagnosis because it is a benign lesion and complete surgical resection is curative.