MacMillan A R, Oliver A J, Reade P C, Marshall D R
Section of Oral Medicine & Oral Surgery, School of Dental Science, University of Melbourne, Victoria, Australia.
Int J Oral Maxillofac Surg. 1990 Oct;19(5):283-6. doi: 10.1016/s0901-5027(05)80421-7.
Congenital infiltrating lipomatosis of the face (CIL-F) is a rare lesion. Presented here is a review of the literature concerning this condition, with the report of a case with clinical signs indistinguishable from those of unilateral facial hyperplasia. Previously unreported clinical and radiographic features of regional bony hypertrophy and macrodontia associated with this case of CIL-F are described and the proposition raised that previously reported cases of unilateral facial hyperplasia may have been due to CIL-F. It is suggested that the clinical findings in this case of facial asymmetry associated with CIL-F, regional macrodontia and regional bony enlargement may constitute a previously undescribed syndrome.
先天性面部浸润性脂肪瘤（CIL-F）是一种罕见的病变。本文对有关该病症的文献进行了综述，并报告了一例临床体征与单侧面部增生难以区分的病例。描述了与该例CIL-F相关的区域骨肥大和巨牙症的先前未报道的临床和影像学特征，并提出先前报道的单侧面部增生病例可能是由CIL-F引起的。有人认为，该例与CIL-F相关的面部不对称、区域巨牙症和区域骨增大的临床发现可能构成一种先前未描述的综合征。
