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Primary mediastinal hemangiopericytoma

BACKGROUND: Hemangiopericytoma is a rare mesenchymal neoplasm, accounting for about 1% of vascular tumors The tumor occurs most commonly in the skin, subcutaneous soft tissues, muscles of the extremities, retroperitoneum but rarely in the lung, trachea or mediastinum. CASE PRESENTATION: A rare case...

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Detalles Bibliográficos
Autores principales: Chnaris, A, Barbetakis, N, Efstathiou, A, Fessatidis, I
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1459159/
https://www.ncbi.nlm.nih.gov/pubmed/16643656
http://dx.doi.org/10.1186/1477-7819-4-23
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author Chnaris, A
Barbetakis, N
Efstathiou, A
Fessatidis, I
author_facet Chnaris, A
Barbetakis, N
Efstathiou, A
Fessatidis, I
author_sort Chnaris, A
collection PubMed
description BACKGROUND: Hemangiopericytoma is a rare mesenchymal neoplasm, accounting for about 1% of vascular tumors The tumor occurs most commonly in the skin, subcutaneous soft tissues, muscles of the extremities, retroperitoneum but rarely in the lung, trachea or mediastinum. CASE PRESENTATION: A rare case of primary mediastinal hemangiopericytoma is presented. A 72-year-old woman was treated by complete surgical resection of the tumor. Details of the clinical and radiographic feature are presented. The patient's postoperative course was uneventful with no evidence of recurrence 9 months after the operation. CONCLUSION: Hemangiopericytoma is an uncommon, potentially malignant tumor originating from pericytes in the small vessels and surgical radical excision is the treatment of choice, although the criteria for determining the area of resection have not been established. International literature has demonstrated that recurrent disease usually occurs within 2 years and therefore a long-term careful follow-up is required.
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spelling pubmed-14591592006-05-11 Primary mediastinal hemangiopericytoma Chnaris, A Barbetakis, N Efstathiou, A Fessatidis, I World J Surg Oncol Case Report BACKGROUND: Hemangiopericytoma is a rare mesenchymal neoplasm, accounting for about 1% of vascular tumors The tumor occurs most commonly in the skin, subcutaneous soft tissues, muscles of the extremities, retroperitoneum but rarely in the lung, trachea or mediastinum. CASE PRESENTATION: A rare case of primary mediastinal hemangiopericytoma is presented. A 72-year-old woman was treated by complete surgical resection of the tumor. Details of the clinical and radiographic feature are presented. The patient's postoperative course was uneventful with no evidence of recurrence 9 months after the operation. CONCLUSION: Hemangiopericytoma is an uncommon, potentially malignant tumor originating from pericytes in the small vessels and surgical radical excision is the treatment of choice, although the criteria for determining the area of resection have not been established. International literature has demonstrated that recurrent disease usually occurs within 2 years and therefore a long-term careful follow-up is required. BioMed Central 2006-04-27 /pmc/articles/PMC1459159/ /pubmed/16643656 http://dx.doi.org/10.1186/1477-7819-4-23 Text en Copyright © 2006 Chnaris et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chnaris, A
Barbetakis, N
Efstathiou, A
Fessatidis, I
Primary mediastinal hemangiopericytoma
title Primary mediastinal hemangiopericytoma
title_full Primary mediastinal hemangiopericytoma
title_fullStr Primary mediastinal hemangiopericytoma
title_full_unstemmed Primary mediastinal hemangiopericytoma
title_short Primary mediastinal hemangiopericytoma
title_sort primary mediastinal hemangiopericytoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1459159/
https://www.ncbi.nlm.nih.gov/pubmed/16643656
http://dx.doi.org/10.1186/1477-7819-4-23
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