Peter A. Reichart , Hans Peter Philipsen , Alexander Moegelin , Uwe Thalmann
{"title":"中枢性牙源性纤维瘤,颗粒细胞变异","authors":"Peter A. Reichart , Hans Peter Philipsen , Alexander Moegelin , Uwe Thalmann","doi":"10.1016/j.ooe.2005.05.007","DOIUrl":null,"url":null,"abstract":"<div><p>A case of central odontogenic fibroma (COF) of the <em>epithelium-rich</em> type (granular cell variant) is reported. A 46-year-old female, demonstrated a multilocular, septated radiolucency below and between the roots of the teeth in 44–47 region. On microscopy the lesion revealed an odontogenic fibroma of the <em>epithelium-rich</em> type with areas characterized by lobules of spherical cells of varying size containing fine S-100 negative granules. In addition, scattered foci of cementoid/osteoid calcified material occurred. Based on several studies, the present authors entertain the hypothesis that supports a histiocystic origin the granular cells. Therapy consisted of curettage of the lesion. The defect was filled with spongeous bone. No recurrence occurred after follow-up of two years.</p></div>","PeriodicalId":100990,"journal":{"name":"Oral Oncology Extra","volume":"42 1","pages":"Pages 5-9"},"PeriodicalIF":0.0000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ooe.2005.05.007","citationCount":"23","resultStr":"{\"title\":\"Central odontogenic fibroma, granular cell variant\",\"authors\":\"Peter A. Reichart , Hans Peter Philipsen , Alexander Moegelin , Uwe Thalmann\",\"doi\":\"10.1016/j.ooe.2005.05.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A case of central odontogenic fibroma (COF) of the <em>epithelium-rich</em> type (granular cell variant) is reported. A 46-year-old female, demonstrated a multilocular, septated radiolucency below and between the roots of the teeth in 44–47 region. On microscopy the lesion revealed an odontogenic fibroma of the <em>epithelium-rich</em> type with areas characterized by lobules of spherical cells of varying size containing fine S-100 negative granules. In addition, scattered foci of cementoid/osteoid calcified material occurred. Based on several studies, the present authors entertain the hypothesis that supports a histiocystic origin the granular cells. Therapy consisted of curettage of the lesion. The defect was filled with spongeous bone. No recurrence occurred after follow-up of two years.</p></div>\",\"PeriodicalId\":100990,\"journal\":{\"name\":\"Oral Oncology Extra\",\"volume\":\"42 1\",\"pages\":\"Pages 5-9\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.ooe.2005.05.007\",\"citationCount\":\"23\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oral Oncology Extra\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1741940905000427\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral Oncology Extra","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1741940905000427","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Central odontogenic fibroma, granular cell variant
A case of central odontogenic fibroma (COF) of the epithelium-rich type (granular cell variant) is reported. A 46-year-old female, demonstrated a multilocular, septated radiolucency below and between the roots of the teeth in 44–47 region. On microscopy the lesion revealed an odontogenic fibroma of the epithelium-rich type with areas characterized by lobules of spherical cells of varying size containing fine S-100 negative granules. In addition, scattered foci of cementoid/osteoid calcified material occurred. Based on several studies, the present authors entertain the hypothesis that supports a histiocystic origin the granular cells. Therapy consisted of curettage of the lesion. The defect was filled with spongeous bone. No recurrence occurred after follow-up of two years.