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Congenital diffuse infiltrating facial lipomatosis

Congenital diffuse infiltrating lipomatosis of the face (CDIL-F) is a rare pathological entity belonging to the subgroup of lipomatous tumors. Till date only a handful of cases has been documented and known to occur exclusively in infancy. On microscopical examination, it is characterized by diffuse...

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Autor principal: Balaji, S. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591063/
https://www.ncbi.nlm.nih.gov/pubmed/23483013
http://dx.doi.org/10.4103/2231-0746.101363
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author Balaji, S. M.
author_facet Balaji, S. M.
author_sort Balaji, S. M.
collection PubMed
description Congenital diffuse infiltrating lipomatosis of the face (CDIL-F) is a rare pathological entity belonging to the subgroup of lipomatous tumors. Till date only a handful of cases has been documented and known to occur exclusively in infancy. On microscopical examination, it is characterized by diffuse infiltration of mature adipose tissue over normal muscle fibers, rapid growth, associated osseous hyperplasia, and a high recurrence rate after surgical intervention. An attempt has been made to identify and characterize all the 49 documented cases of CDIL-F in literature along with describing a report of a male child with CDIL-F. Follow-up of 8 years has been documented. The pathogenesis and spectrum of treatment modality are discussed with identified clinical features.
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spelling pubmed-35910632013-03-11 Congenital diffuse infiltrating facial lipomatosis Balaji, S. M. Ann Maxillofac Surg Case Report - Developmental Disorder Congenital diffuse infiltrating lipomatosis of the face (CDIL-F) is a rare pathological entity belonging to the subgroup of lipomatous tumors. Till date only a handful of cases has been documented and known to occur exclusively in infancy. On microscopical examination, it is characterized by diffuse infiltration of mature adipose tissue over normal muscle fibers, rapid growth, associated osseous hyperplasia, and a high recurrence rate after surgical intervention. An attempt has been made to identify and characterize all the 49 documented cases of CDIL-F in literature along with describing a report of a male child with CDIL-F. Follow-up of 8 years has been documented. The pathogenesis and spectrum of treatment modality are discussed with identified clinical features. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3591063/ /pubmed/23483013 http://dx.doi.org/10.4103/2231-0746.101363 Text en Copyright: © Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report - Developmental Disorder
Balaji, S. M.
Congenital diffuse infiltrating facial lipomatosis
title Congenital diffuse infiltrating facial lipomatosis
title_full Congenital diffuse infiltrating facial lipomatosis
title_fullStr Congenital diffuse infiltrating facial lipomatosis
title_full_unstemmed Congenital diffuse infiltrating facial lipomatosis
title_short Congenital diffuse infiltrating facial lipomatosis
title_sort congenital diffuse infiltrating facial lipomatosis
topic Case Report - Developmental Disorder
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591063/
https://www.ncbi.nlm.nih.gov/pubmed/23483013
http://dx.doi.org/10.4103/2231-0746.101363
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