先天性面部浸润性脂肪瘤病x线表现1例。

Q3 Dentistry

Frontiers in Dentistry Pub Date : 2022-08-11 eCollection Date: 2022-01-01 DOI:10.18502/fid.v19i27.10598

Hoorieh Bashizadehfakhar, Mehrdad Panjnoush, Yasaman Kheirandish, Azin Sedaghati, Faezeh Mirjalili, Sara Aliasghari Abandansari

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引用次数: 0

摘要

先天性弥漫性浸润性面部脂肪瘤病(cdi - f)是一种罕见的临床病理实体，病因不明，成熟脂肪组织浸润一侧软组织结构，造成相当不对称。在此，我们报告一位在12年间接受多次外科手术却没有明确诊断的cdi - f病例。由于脂肪组织的浸润使清除困难，cdi - f表现出不同程度的严重症状。因此，建议告知患者高复发率。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Radiographic Findings of Congenital Facial Infiltrating Lipomatosis: A Case Report.

查看原文本刊更多论文

Radiographic Findings of Congenital Facial Infiltrating Lipomatosis: A Case Report.

Congenital diffuse infiltrating lipomatosis of the face (CDIL-F) is a rare clinicopathological entity with an unknown etiology, in which mature adipose tissue infiltrates the soft tissue structures in one side, and causes considerable asymmetry. Herein, we report a case of CDIL-F who underwent many surgical procedures without definite diagnosis during 12 years. CDIL-F presents symptoms with various severity levels due to infiltration of adipose tissue that makes removal difficult. Thus, it is recommended to inform patients about the high rate of recurrence.

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来源期刊

Frontiers in Dentistry Dentistry-General Dentistry

CiteScore

1.00

自引率

0.00%

发文量

审稿时长

12 weeks