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Sinonasal hemangiopericytoma: A rare case report with review of literature

Hemangiopericytoma (HPC) is a rare tumor of uncertain malignant potential. Stout and Murray described HPC as “vascular tumor arising from Zimmerman's pericyte” in 1942. The World Health Organization (WHO) reclassified HPC as a fibroblastic/myofibroblastic tumor, after further characterization....

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Autores principales: Shobha, BV, Shivakumar, BN, Reddy, Santhosh, Dutta, Neerav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451651/
https://www.ncbi.nlm.nih.gov/pubmed/26097321
http://dx.doi.org/10.4103/0973-029X.157214
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author Shobha, BV
Shivakumar, BN
Reddy, Santhosh
Dutta, Neerav
author_facet Shobha, BV
Shivakumar, BN
Reddy, Santhosh
Dutta, Neerav
author_sort Shobha, BV
collection PubMed
description Hemangiopericytoma (HPC) is a rare tumor of uncertain malignant potential. Stout and Murray described HPC as “vascular tumor arising from Zimmerman's pericyte” in 1942. The World Health Organization (WHO) reclassified HPC as a fibroblastic/myofibroblastic tumor, after further characterization. HPC is found mostly wherever there is increased vascularity seen. The incidence of the tumor in head and neck area is only 15%, mostly seen in adults. We report here a case of HPC of a 22-year-old female, who presented to our department with a tender swelling in maxillary anterior region and the mass was well-circumscribed, sessile and soft on palpation. The skin over the tumor was intact and normal. The tumor was completely removed with wide surgical resection. The histopathological staining supported the diagnosis of HPC, this was further confirmed by immunohistochemistry (IHC) in which CD99 showed strong positivity.
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spelling pubmed-44516512015-06-19 Sinonasal hemangiopericytoma: A rare case report with review of literature Shobha, BV Shivakumar, BN Reddy, Santhosh Dutta, Neerav J Oral Maxillofac Pathol Case Report Hemangiopericytoma (HPC) is a rare tumor of uncertain malignant potential. Stout and Murray described HPC as “vascular tumor arising from Zimmerman's pericyte” in 1942. The World Health Organization (WHO) reclassified HPC as a fibroblastic/myofibroblastic tumor, after further characterization. HPC is found mostly wherever there is increased vascularity seen. The incidence of the tumor in head and neck area is only 15%, mostly seen in adults. We report here a case of HPC of a 22-year-old female, who presented to our department with a tender swelling in maxillary anterior region and the mass was well-circumscribed, sessile and soft on palpation. The skin over the tumor was intact and normal. The tumor was completely removed with wide surgical resection. The histopathological staining supported the diagnosis of HPC, this was further confirmed by immunohistochemistry (IHC) in which CD99 showed strong positivity. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4451651/ /pubmed/26097321 http://dx.doi.org/10.4103/0973-029X.157214 Text en Copyright: © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Shobha, BV
Shivakumar, BN
Reddy, Santhosh
Dutta, Neerav
Sinonasal hemangiopericytoma: A rare case report with review of literature
title Sinonasal hemangiopericytoma: A rare case report with review of literature
title_full Sinonasal hemangiopericytoma: A rare case report with review of literature
title_fullStr Sinonasal hemangiopericytoma: A rare case report with review of literature
title_full_unstemmed Sinonasal hemangiopericytoma: A rare case report with review of literature
title_short Sinonasal hemangiopericytoma: A rare case report with review of literature
title_sort sinonasal hemangiopericytoma: a rare case report with review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451651/
https://www.ncbi.nlm.nih.gov/pubmed/26097321
http://dx.doi.org/10.4103/0973-029X.157214
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