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Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations
Fibrous dysplasia (FD) of bone is a benign, congenital and rare disease in which normal bone is replaced by fibrous bone tissue, resulting in bone deformities. It can affect any bone in the body, however craniofacial fibrous dysplasia is characterized by specific clinical manifestations, progression...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864254/ https://www.ncbi.nlm.nih.gov/pubmed/33598085 http://dx.doi.org/10.11604/pamj.2020.37.271.21350 |
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author | Lame, Cheikh Ahmedou Loum, Birame Diallo, Thierno Boubacar Ndiaye, Cheikhna Ba Diouf, Khady Marie Agnès Fall, Amat |
author_facet | Lame, Cheikh Ahmedou Loum, Birame Diallo, Thierno Boubacar Ndiaye, Cheikhna Ba Diouf, Khady Marie Agnès Fall, Amat |
author_sort | Lame, Cheikh Ahmedou |
collection | PubMed |
description | Fibrous dysplasia (FD) of bone is a benign, congenital and rare disease in which normal bone is replaced by fibrous bone tissue, resulting in bone deformities. It can affect any bone in the body, however craniofacial fibrous dysplasia is characterized by specific clinical manifestations, progression and therapeutic issues. The purpose of our study was to describe the diagnostic, therapeutic and evolutionary features of craniofacial FD. This study involved six patients with craniofacial FD followed up in the Department of Otolaryngology at the Principal Hospital of Dakar. The average age of patients was 26.16 years, ranging from 11 to 58 years. Sex ratio favoured women (83% of the cases). Bone deformity was the main feature of craniofacial FD leading to diagnosis. One patient presented with unilateral nasal obstruction with epistaxis. In all cases, scanner enabled diagnosis and topographic balance. Two female patients underwent surgery. One case of recurrence was reported. Craniofacial FD is a rare bone disease that can manifest as serious sensory and functional disorders. It poses real therapeutic issues; hence adequate interdisciplinar management is essential. |
format | Online Article Text |
id | pubmed-7864254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-78642542021-02-16 Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations Lame, Cheikh Ahmedou Loum, Birame Diallo, Thierno Boubacar Ndiaye, Cheikhna Ba Diouf, Khady Marie Agnès Fall, Amat Pan Afr Med J Case Series Fibrous dysplasia (FD) of bone is a benign, congenital and rare disease in which normal bone is replaced by fibrous bone tissue, resulting in bone deformities. It can affect any bone in the body, however craniofacial fibrous dysplasia is characterized by specific clinical manifestations, progression and therapeutic issues. The purpose of our study was to describe the diagnostic, therapeutic and evolutionary features of craniofacial FD. This study involved six patients with craniofacial FD followed up in the Department of Otolaryngology at the Principal Hospital of Dakar. The average age of patients was 26.16 years, ranging from 11 to 58 years. Sex ratio favoured women (83% of the cases). Bone deformity was the main feature of craniofacial FD leading to diagnosis. One patient presented with unilateral nasal obstruction with epistaxis. In all cases, scanner enabled diagnosis and topographic balance. Two female patients underwent surgery. One case of recurrence was reported. Craniofacial FD is a rare bone disease that can manifest as serious sensory and functional disorders. It poses real therapeutic issues; hence adequate interdisciplinar management is essential. The African Field Epidemiology Network 2020-11-25 /pmc/articles/PMC7864254/ /pubmed/33598085 http://dx.doi.org/10.11604/pamj.2020.37.271.21350 Text en Copyright: Cheikh Ahmedou Lame et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Series Lame, Cheikh Ahmedou Loum, Birame Diallo, Thierno Boubacar Ndiaye, Cheikhna Ba Diouf, Khady Marie Agnès Fall, Amat Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
title | Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
title_full | Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
title_fullStr | Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
title_full_unstemmed | Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
title_short | Dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
title_sort | dysplasie fibreuse osseuse crânio-faciale: à propos de six observations |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864254/ https://www.ncbi.nlm.nih.gov/pubmed/33598085 http://dx.doi.org/10.11604/pamj.2020.37.271.21350 |
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