Raphael Hart Lyngdoh; Sumanth Devaraju; Leena JB
Volume 8, Issue 1 , January 2013, , Pages 45-47
Abstract
Hamartomatous polyps of the palatine tonsil are very rare. They have been variously termed as a lymphangiectatic fibrous polyp, lipoma, pedunculated tonsil etc. in the English literature. We present here a case of hamartomatous polyp of the tonsil occurring in a 32-year-old male who presented ...
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Hamartomatous polyps of the palatine tonsil are very rare. They have been variously termed as a lymphangiectatic fibrous polyp, lipoma, pedunculated tonsil etc. in the English literature. We present here a case of hamartomatous polyp of the tonsil occurring in a 32-year-old male who presented with bilateral enlarged palatine tonsils with recurrent tonsillitis. Surgical excision showed two pale brown nodular tissue bits, larger measuring 4x3x1 cm and smaller measuring 3.5x2.5x1.5 cm. An irregular pedunculated polypoidal tissue measuring 1.5x1x0.8cm was seen attached to the smaller mass, the cut surface of which showed pale white, lobulated areas. On histological examination, the polyp showed lining by stratified squamous epithelium and was composed of fibrocollagenous stroma with many dilated blood vessels, adipocytes, subepithelial lymphoid aggregates and benign mucinous glands suggestive of a hamartomatous polyp. Both the tonsils showed features of chronic tonsillitis.
Zhaleh Mohsenifar1; Nazanin Mahdavi; Sara Bagheri
Volume 8, Issue 1 , January 2013, , Pages 48-54
Abstract
Lymphoepithelial cyst of oral cavity is a rare cystic lesion that presents as an asymptomatic submucosal mass and is usually discovered during routine dental examinations. The site most commonly affected is floor of the mouth and tonsillar involvement seems to be very rare. Multiple Lymphoepithelial ...
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Lymphoepithelial cyst of oral cavity is a rare cystic lesion that presents as an asymptomatic submucosal mass and is usually discovered during routine dental examinations. The site most commonly affected is floor of the mouth and tonsillar involvement seems to be very rare. Multiple Lymphoepithelial cysts have been reported in parotid of HIV positive patients however in oral cavity they usually present as solitary lesions.We report a case of multiple bilateral Lymphoepithelial cysts of the palatine tonsils in a 72 years old male that presents with fever, pain and obstructive sleep apnea.We didn’t find any bilateral or multiple tonsillar lymphoepiyhelial cysts in the literature and the present paper seems to be the first report. We suggest although lymphoepithelial cysts rarely occur in the tonsils but they should be considered in differential diagnosis of adenotonsillar enlargement and related obstructive sleep apnea.
