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Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report
INTRODUCTION: Maxillomandibular sygnathia is a rare and severe craniofacial deformity defined by gingival mucosal fusion (synechia) or bony fusion (synostosis). CASE REPORT: We will present a case of complete closure of the mouth since birth from eastern Morocco treated in our department of maxillof...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259410/ https://www.ncbi.nlm.nih.gov/pubmed/34225063 http://dx.doi.org/10.1016/j.ijscr.2021.106078 |
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author | Raiteb, Mohamed Elmrini, Sanaa Hassani, Fatemazahra Azami Maadane, Amina Slimani, Faiçal |
author_facet | Raiteb, Mohamed Elmrini, Sanaa Hassani, Fatemazahra Azami Maadane, Amina Slimani, Faiçal |
author_sort | Raiteb, Mohamed |
collection | PubMed |
description | INTRODUCTION: Maxillomandibular sygnathia is a rare and severe craniofacial deformity defined by gingival mucosal fusion (synechia) or bony fusion (synostosis). CASE REPORT: We will present a case of complete closure of the mouth since birth from eastern Morocco treated in our department of maxillofacial surgery at the University Hospital of Casablanca. The patient was referred after two months by the pediatrician of the provincial hospital and following the placement of a nasogastric tube. On admission, she presented with facial dysmorphosis, signs of malnutrition with closure of the mouth and fusion of both gums with pro-alveoli and retromandibulia. CT scan with 3D reconstruction confirmed maxillomandibular synostosis. 5 days later, she underwent a fixed mucosal incision with osteotomy at the maxillomandibular joints with early and prolonged active physical therapy. The evolution was marked by the recurrence of mouth closure, the little girl was operated a second time and then she died by a mucous plug at the level of her tracheostomy cannula during resuscitation. DISCUSSION: Maxillomandibular sygnathia is a very rare pathology whose origin remains unknown. Very few cases published in the literature. CONCLUSION: The therapeutic difficulties encountered outside the ideal age of the operation and the management of recurrences were also linked to socio-economic factors making it difficult to ensure adequate postoperative follow-up. |
format | Online Article Text |
id | pubmed-8259410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82594102021-07-12 Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report Raiteb, Mohamed Elmrini, Sanaa Hassani, Fatemazahra Azami Maadane, Amina Slimani, Faiçal Int J Surg Case Rep Case Report INTRODUCTION: Maxillomandibular sygnathia is a rare and severe craniofacial deformity defined by gingival mucosal fusion (synechia) or bony fusion (synostosis). CASE REPORT: We will present a case of complete closure of the mouth since birth from eastern Morocco treated in our department of maxillofacial surgery at the University Hospital of Casablanca. The patient was referred after two months by the pediatrician of the provincial hospital and following the placement of a nasogastric tube. On admission, she presented with facial dysmorphosis, signs of malnutrition with closure of the mouth and fusion of both gums with pro-alveoli and retromandibulia. CT scan with 3D reconstruction confirmed maxillomandibular synostosis. 5 days later, she underwent a fixed mucosal incision with osteotomy at the maxillomandibular joints with early and prolonged active physical therapy. The evolution was marked by the recurrence of mouth closure, the little girl was operated a second time and then she died by a mucous plug at the level of her tracheostomy cannula during resuscitation. DISCUSSION: Maxillomandibular sygnathia is a very rare pathology whose origin remains unknown. Very few cases published in the literature. CONCLUSION: The therapeutic difficulties encountered outside the ideal age of the operation and the management of recurrences were also linked to socio-economic factors making it difficult to ensure adequate postoperative follow-up. Elsevier 2021-06-22 /pmc/articles/PMC8259410/ /pubmed/34225063 http://dx.doi.org/10.1016/j.ijscr.2021.106078 Text en © 2021 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Raiteb, Mohamed Elmrini, Sanaa Hassani, Fatemazahra Azami Maadane, Amina Slimani, Faiçal Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report |
title | Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report |
title_full | Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report |
title_fullStr | Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report |
title_full_unstemmed | Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report |
title_short | Congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: Case report |
title_sort | congenital bilateral zygomatico-maxillo-mandibular fusion associated with gumfusion: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259410/ https://www.ncbi.nlm.nih.gov/pubmed/34225063 http://dx.doi.org/10.1016/j.ijscr.2021.106078 |
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