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Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report
BACKGROUND: Mandibular pseudocarcinomatous hyperplasia is a rare and generally benign pathology. We report on one of these rare cases. CASE PRESENTATION: The case history of a 73-year-old white man stated that he had a carcinoma of the oropharynx, which was primarily treated with radiotherapy and ch...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041521/ https://www.ncbi.nlm.nih.gov/pubmed/27680099 http://dx.doi.org/10.1186/s13256-016-1052-y |
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author | Fuchs, Andreas Hartmann, Stefan Ernestus, Karen Mutzbauer, Grit Linz, Christian Brands, Roman C. Kübler, Alexander C. Müller-Richter, Urs D. A. |
author_facet | Fuchs, Andreas Hartmann, Stefan Ernestus, Karen Mutzbauer, Grit Linz, Christian Brands, Roman C. Kübler, Alexander C. Müller-Richter, Urs D. A. |
author_sort | Fuchs, Andreas |
collection | PubMed |
description | BACKGROUND: Mandibular pseudocarcinomatous hyperplasia is a rare and generally benign pathology. We report on one of these rare cases. CASE PRESENTATION: The case history of a 73-year-old white man stated that he had a carcinoma of the oropharynx, which was primarily treated with radiotherapy and chemotherapy 4 years prior. As a result of radiotherapy he developed an osteoradionecrosis of his mandible and a consecutive pathological fracture of his left mandibular angle. Subsequent osteosynthesis was performed with a reconstruction plate. When we first saw him, his reconstruction plate was partially exposed with intraoral and extraoral fistulation. The resected bone of his defect-bordering jaw showed the typical pathohistological findings of an intraosseous mandibular pseudocarcinomatous hyperplasia. After a first reconstruction attempt with an iliac crest graft failed, definitive reconstruction of his mandible with a microvascular anastomosed fibula graft was achieved. CONCLUSIONS: Intraosseous pseudocarcinomatous hyperplasia of the mandible is a rare differential diagnosis in maxillofacial surgery. Besides other benign epithelial neoplasms, such as calcifying epithelial odontogenic tumor, squamous odontogenic tumor, or different forms of ameloblastoma, the far more frequent invasive squamous cell carcinoma needs to be excluded. A misinterpretation of pseudocarcinomatous hyperplasia as squamous cell carcinoma must be avoided because it can lead to a massive overtreatment. |
format | Online Article Text |
id | pubmed-5041521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50415212016-10-05 Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report Fuchs, Andreas Hartmann, Stefan Ernestus, Karen Mutzbauer, Grit Linz, Christian Brands, Roman C. Kübler, Alexander C. Müller-Richter, Urs D. A. J Med Case Rep Case Report BACKGROUND: Mandibular pseudocarcinomatous hyperplasia is a rare and generally benign pathology. We report on one of these rare cases. CASE PRESENTATION: The case history of a 73-year-old white man stated that he had a carcinoma of the oropharynx, which was primarily treated with radiotherapy and chemotherapy 4 years prior. As a result of radiotherapy he developed an osteoradionecrosis of his mandible and a consecutive pathological fracture of his left mandibular angle. Subsequent osteosynthesis was performed with a reconstruction plate. When we first saw him, his reconstruction plate was partially exposed with intraoral and extraoral fistulation. The resected bone of his defect-bordering jaw showed the typical pathohistological findings of an intraosseous mandibular pseudocarcinomatous hyperplasia. After a first reconstruction attempt with an iliac crest graft failed, definitive reconstruction of his mandible with a microvascular anastomosed fibula graft was achieved. CONCLUSIONS: Intraosseous pseudocarcinomatous hyperplasia of the mandible is a rare differential diagnosis in maxillofacial surgery. Besides other benign epithelial neoplasms, such as calcifying epithelial odontogenic tumor, squamous odontogenic tumor, or different forms of ameloblastoma, the far more frequent invasive squamous cell carcinoma needs to be excluded. A misinterpretation of pseudocarcinomatous hyperplasia as squamous cell carcinoma must be avoided because it can lead to a massive overtreatment. BioMed Central 2016-09-29 /pmc/articles/PMC5041521/ /pubmed/27680099 http://dx.doi.org/10.1186/s13256-016-1052-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Fuchs, Andreas Hartmann, Stefan Ernestus, Karen Mutzbauer, Grit Linz, Christian Brands, Roman C. Kübler, Alexander C. Müller-Richter, Urs D. A. Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
title | Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
title_full | Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
title_fullStr | Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
title_full_unstemmed | Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
title_short | Mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
title_sort | mandibular intraosseous pseudocarcinomatous hyperplasia: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041521/ https://www.ncbi.nlm.nih.gov/pubmed/27680099 http://dx.doi.org/10.1186/s13256-016-1052-y |
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