Gokul S, Ranjini K V, Kirankumar K, Hallikeri K
Department of Oral and Maxillofacial Pathology, SDM College of Dental Sciences and Hospital, Sattur, Dharwad, Karnataka, India.
Int J Oral Maxillofac Surg. 2009 Jan;38(1):91-3. doi: 10.1016/j.ijom.2008.09.005. Epub 2008 Oct 25.
Congenital tumors of the oral cavity are uncommon. Teratoid tumors account for most of the reported cases and are infrequently associated with a cleft of the soft palate. Of the remaining tumors associated with pediatric cleft palate, congenital lipoma is rare. Lipomas of the oral cavity may show cartilaginous or osseous changes. These changes have not been reported in lipoma associated with cleft palate. A rare case of congenital osteolipoma associated with cleft palate and showing osseous change is presented here. The pathogenesis of the lesion and the osseous metaplasia are described. The present case is the second case of congenital lipoma associated with cleft palate in the literature.
口腔先天性肿瘤并不常见。畸胎样肿瘤占报告病例的大多数，且很少与软腭裂相关。在其余与小儿腭裂相关的肿瘤中，先天性脂肪瘤很罕见。口腔脂肪瘤可能会出现软骨或骨质改变。这些改变在与腭裂相关的脂肪瘤中尚未见报道。本文报告1例罕见的与腭裂相关并伴有骨质改变的先天性骨脂肪瘤病例。描述了该病变的发病机制及骨质化生情况。本病例是文献中第二例与腭裂相关的先天性脂肪瘤。
