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先天性面部浸润性脂肪瘤病的影像学表现:一例报告

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

作者信息

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

机构信息

Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

Department of Dentomaxillofacial Radiology, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Front Dent. 2022 Aug 11;19:27. doi: 10.18502/fid.v19i27.10598. eCollection 2022.

DOI:10.18502/fid.v19i27.10598
PMID:36458277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9675623/
Abstract

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.

摘要

先天性面部弥漫性浸润性脂肪瘤病(CDIL-F)是一种病因不明的罕见临床病理实体,其中成熟脂肪组织浸润一侧的软组织结构,导致明显的不对称。在此,我们报告一例CDIL-F患者,其在12年中接受了多次手术,但未得到明确诊断。由于脂肪组织浸润,CDIL-F的症状严重程度各异,这使得切除困难。因此,建议告知患者复发率较高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/36044cd8a37b/FID-19-27-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/7fd46a28129c/FID-19-27-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/df687bf4dbad/FID-19-27-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/36044cd8a37b/FID-19-27-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/7fd46a28129c/FID-19-27-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/df687bf4dbad/FID-19-27-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed86/9675623/36044cd8a37b/FID-19-27-g003.jpg

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本文引用的文献

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Congenital Infiltrating Lipomatosis of the Face: Case Report and Literature Review.先天性面部浸润性脂肪瘤:病例报告及文献综述
Ann Plast Surg. 2018 Jan;80(1):83-89. doi: 10.1097/SAP.0000000000001213.
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Congenital infiltrating lipomatosis of the face: A case report with review of literature.先天性面部浸润性脂肪瘤:一例报告并文献复习
Indian Dermatol Online J. 2014 Jul;5(3):303-5. doi: 10.4103/2229-5178.137783.
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PIK3CA activating mutations in facial infiltrating lipomatosis.面部浸润性脂肪瘤病中的 PIK3CA 激活突变。
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Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1.一名患有1号染色体1q24.3q31.1缺失的女孩出现垂体功能减退和先天性面部浸润性脂肪瘤病。
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Interdisciplinary management of congenital infiltrating lipomatosis.先天性浸润性脂肪瘤病的多学科管理
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Case Rep Pediatr. 2012;2012:134646. doi: 10.1155/2012/134646. Epub 2012 Apr 2.
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Congenital infiltrating lipomatosis of the face with exophytic temporomandibular joint ankylosis: a case report and review of the literature.先天性面部浸润性脂肪瘤病伴外生性颞下颌关节强直:病例报告及文献复习。
Dentomaxillofac Radiol. 2013;42(3):16128745. doi: 10.1259/dmfr/16128745. Epub 2012 Jan 12.
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Int J Surg Case Rep. 2011;2(7):201-5. doi: 10.1016/j.ijscr.2011.06.007. Epub 2011 Jun 29.