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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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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. |
format | Online Article Text |
id | pubmed-3591063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT balajism congenitaldiffuseinfiltratingfaciallipomatosis |