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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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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. |
format | Online Article Text |
id | pubmed-4165562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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