面部先天性浸润型脂肪增殖症2例及文献回顾  

Congenital infiltrating lipomatosis of face:Two cases reports and review

作　　者：吴滢倩 苏吉梅[1] Wu Yingqian;Su Jimei(Department of Stomatology,Children's Hospital,Zhejiang University School of Medicine,National Clinical Research Center for Child Health,Hangzhou 310052,China)

机构地区：[1]浙江大学医学院附属儿童医院口腔科,国家儿童健康与疾病临床医学研究中心,杭州310052

出　　处：《中华口腔医学研究杂志（电子版）》2024年第1期48-53,共6页Chinese Journal of Stomatological Research(Electronic Edition)

摘　　要：面部先天性浸润型脂肪增殖症(CILF)是一种先天性、非遗传性、浸润性脂肪组织增多的罕见病变。CILF多在出生时发现,主要临床表现为明显的面部软组织膨隆,部分患者伴发受累侧颌骨膨隆、恒牙早萌和过大牙等,易累及面下2/3,左侧多见。影像学表现为受累侧面部软组织脂肪浸润。本文报道2例CILF,并对其病因、临床表现、诊断和治疗进展作一综述。Congenital infiltrating lipomatosis of face(CILF)is a rare disease that is congenital,non-hereditary,and increased infiltrating adipose tissue.CILF is mostly found at birth,with the main clinical manifestations of obvious facial soft tissue swelling,jaw bone swelling,early eruption of permanent teeth,macrodontism,etc.It is often occurring to the lower 2/3 parts of the face,and the left side.Imaging examination shows fatty infiltration of soft tissues in the affected face.This article reported two cases of CILF,and reviewed its etiology,clinical mani festations,diagnosis,and treatment progress.

关 键 词：面部先天性浸润型脂肪增殖症 面部增生 恒牙早萌 巨大牙 

分 类 号：R78[医药卫生—口腔医学]