AVRAAM, Konstantinos, ZACHARIS, E., ALMPANIS, Z., CHALEPLIDIS, N., GIOVANITIS, D., BARBOUNIS, T., Zyli, I., TSANTOPOULOS, M., and REVELOS, K.
PURPOSE: To report a case of granulomatous cheilitis and to emphasize the importance of its diagnosis. MATERIAL/METHODS: A 38 year-old female patient with a disease-free medical history underwent a biopsy of the upper left lip due to a longterm, rapidly growing , painless, recurrent enlargement in the anatomic area for the past two months. The surgical specimen was fi xed in formalin , the samples were embedded in paraffi n blocks and histologic sections were taken and stain with hematoxylin- eosin. RESULTS: Histopathologic examination revealed oral mucosal with small sized epithelioid granulomas without central necrosis with characteristic giant cells of Langhans type and the accompinying presence of lymphocytic infi ltration within swelling stroma. ISTOCHEMICAL STAINS : PAS (-) , Giemsa (-) , Ziehl-Nielsen (-) These fi ndings were not specifi c and suggested the diagnosis of granulomatous cheilitis. CONCLUSION: Granulomatous cheilitis is a rare chronic infl ammatory disease of unknown origin characterized of the swelling of one or both lips. It belongs to a group of diseases known as orophacial granulomatosis in which sarcoidosis , tuberculosis , Crohn disease , Melkersson-Rosenthal syndrome and infectious diseases such as brucellosis are included. Idiopathic granulomatous cheilitis is a diagnosis of exclusion and in order to certify this uncommon entity the full knowledge of the preoperative patients‘ medical history, physical and histological examination and laboratory tests are necessary. [ABSTRACT FROM AUTHOR]