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Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report

Inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion found in the maxillofacial region. Its frequency diminishes further when found in the bone. Although classification has varied throughout its history, the histologic features are often diagnostic, particularly with its strong assoc...

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Detalles Bibliográficos
Autores principales: Stringer, Dale E., Allen, Chad N., Nguyen, Katina, Tandon, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165562/
https://www.ncbi.nlm.nih.gov/pubmed/25254136
http://dx.doi.org/10.1155/2014/565478
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author Stringer, Dale E.
Allen, Chad N.
Nguyen, Katina
Tandon, Rahul
author_facet Stringer, Dale E.
Allen, Chad N.
Nguyen, Katina
Tandon, Rahul
author_sort Stringer, Dale E.
collection PubMed
description Inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion found in the maxillofacial region. Its frequency diminishes further when found in the bone. Although classification has varied throughout its history, the histologic features are often diagnostic, particularly with its strong association with anaplastic lymphoma kinase-1 (ALK-1) staining. The current mode of treatment for such a lesion is surgical removal with careful followup. In this rare case report, we describe the diagnosis and treatment in a 16-year-old male. Although this rare pathology can present as—and at times mimic—more serious pathologies, it is important for the attending surgeon to initially manage the pathology conservatively.
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spelling pubmed-41655622014-09-24 Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report Stringer, Dale E. Allen, Chad N. Nguyen, Katina Tandon, Rahul Case Rep Surg Case Report Inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion found in the maxillofacial region. Its frequency diminishes further when found in the bone. Although classification has varied throughout its history, the histologic features are often diagnostic, particularly with its strong association with anaplastic lymphoma kinase-1 (ALK-1) staining. The current mode of treatment for such a lesion is surgical removal with careful followup. In this rare case report, we describe the diagnosis and treatment in a 16-year-old male. Although this rare pathology can present as—and at times mimic—more serious pathologies, it is important for the attending surgeon to initially manage the pathology conservatively. Hindawi Publishing Corporation 2014 2014-09-01 /pmc/articles/PMC4165562/ /pubmed/25254136 http://dx.doi.org/10.1155/2014/565478 Text en Copyright © 2014 Dale E. Stringer et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Stringer, Dale E.
Allen, Chad N.
Nguyen, Katina
Tandon, Rahul
Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report
title Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report
title_full Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report
title_fullStr Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report
title_full_unstemmed Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report
title_short Intraosseous Inflammatory Myofibroblastic Tumor in the Mandible: A Rare Pathologic Case Report
title_sort intraosseous inflammatory myofibroblastic tumor in the mandible: a rare pathologic case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165562/
https://www.ncbi.nlm.nih.gov/pubmed/25254136
http://dx.doi.org/10.1155/2014/565478
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