Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis

Congenital infiltrating lipomatosis of the face (CIL-F) is characterized by unilateral diffuse infiltration of facial soft tissue by mature adipose cells with associated skeletal hypertrophy. The disease is also considered a subtype of partial hemifacial hyperplasia. We present a case of right hemif...

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Autores principales: Gupta, Ruchi, Mukul, Sailesh Kumar, Kumar, Prem, Kumar, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518480/
https://www.ncbi.nlm.nih.gov/pubmed/33041589
http://dx.doi.org/10.4103/njms.NJMS_59_17
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author Gupta, Ruchi
Mukul, Sailesh Kumar
Kumar, Prem
Kumar, Amit
author_facet Gupta, Ruchi
Mukul, Sailesh Kumar
Kumar, Prem
Kumar, Amit
author_sort Gupta, Ruchi
collection PubMed
description Congenital infiltrating lipomatosis of the face (CIL-F) is characterized by unilateral diffuse infiltration of facial soft tissue by mature adipose cells with associated skeletal hypertrophy. The disease is also considered a subtype of partial hemifacial hyperplasia. We present a case of right hemifacial swelling with severely restricted mouth opening diagnosed with CIL-F associated with temporomandibular joint ankylosis which is very rare, and very few case reports of the same have been published. Computed tomography findings have been discussed in detail with review of literature.
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spelling pubmed-75184802020-10-09 Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis Gupta, Ruchi Mukul, Sailesh Kumar Kumar, Prem Kumar, Amit Natl J Maxillofac Surg Case Report Congenital infiltrating lipomatosis of the face (CIL-F) is characterized by unilateral diffuse infiltration of facial soft tissue by mature adipose cells with associated skeletal hypertrophy. The disease is also considered a subtype of partial hemifacial hyperplasia. We present a case of right hemifacial swelling with severely restricted mouth opening diagnosed with CIL-F associated with temporomandibular joint ankylosis which is very rare, and very few case reports of the same have been published. Computed tomography findings have been discussed in detail with review of literature. Wolters Kluwer - Medknow 2020 2020-06-18 /pmc/articles/PMC7518480/ /pubmed/33041589 http://dx.doi.org/10.4103/njms.NJMS_59_17 Text en Copyright: © 2020 National Journal of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Gupta, Ruchi
Mukul, Sailesh Kumar
Kumar, Prem
Kumar, Amit
Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
title Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
title_full Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
title_fullStr Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
title_full_unstemmed Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
title_short Congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
title_sort congenital infiltrating lipomatosis of the face with temporomandibular joint ankylosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518480/
https://www.ncbi.nlm.nih.gov/pubmed/33041589
http://dx.doi.org/10.4103/njms.NJMS_59_17
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