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Vol. 62. Issue 3.
Pages 242-245 (May - June 2011)
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Vol. 62. Issue 3.
Pages 242-245 (May - June 2011)
Case study
DOI: 10.1016/j.otorri.2010.02.007
Primary malignant solitary fibrous tumor/hemangiopericytoma of the parotid gland
Tumor fibroso solitario maligno primario/hemangiopericitoma de la glándula parótida
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Oscar Alberto Messa-Boteroa,??
Corresponding author
omessa@cancer.gov.co

Corresponding author.
, Alfredo Ernesto Romero-Rojasa, Sandra Isabel Chinchilla Olayaa, Julio Alexander Díaz-Péreza,b,c, Luis Felipe Tapias-Vargasb
a Group of Pathology, National Institute of Cancer, Bogota, D.C., Colombia
b Research Group in Surgery and Specialties GRICES-UIS, School of Medicine, Universidad Industrial de Santander, Bucaramanga, Colombia
c Fundacion para el Avance de la Anatomia Patologica, Citologia y Clinica Molecular FAPCIM, Bucaramanga, Colombia
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Table 1. Strategy for literature search using MeSH descriptors for MedLine database for other databases an analogue search was performed
Table 2. Immunohistochemistry panel used for the study of the present case
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Abstract

Solitary fibrous tumor (SFT) was first described in the pleura by Lietaud in 1767; later in 1870, Wagner described the localized nature of this type of tumor and Klemperer and Rabin classified pleural tumors into two types: diffuse mesotheliomas and localized mesotheliomas. Recent years have seen the redefinition of this neoplasm, due to better technology; it is now proven that this neoplasm may have multiple different extrapleural origins including the head and neck regions. This diversity of locations is related to the particular mesenchymal histogenesis of SFT which allows its development from very unusual sites such as the salivary glands (SGs). In this particular site, this neoplasm is very infrequent and most of reported cases refer to benign disease, with just one case informed so far of primary malignant SFT.

Keywords:
Solitary fibrous tumor
Parotid gland
Case report
Review
Resumen

El tumor fibroso solitario (TFS) fue primeramente descrito en la pleura por Lietaud en 1767; posteriormente en 1870, Wagner describió la naturaleza localizada de este tipo de tumor y Klemperer y Rabin, en 1931, clasificaron los tumores pleurales en dos tipos: mesoteliomas difusos y mesoteliomas localizados. En los últimos años se ha redefinido esta neoplasia, debido a la mejora de las tecnologías; ahora se ha probado que puede tener múltiples y diferentes orígenes extra-pleurales, incluyendo la región de cabeza y cuello. Esta diversidad de localizaciones se relaciona con la histogénesis mesenquimal particular del TFS, que permite su desarrollo desde localizaciones muy inusuales tales como las glándulas salivares (GS). En esta localización particular este tumor es muy infrecuente, y muchos casos reportados se refieren a una enfermedad benigna, con un único caso informado hasta la fecha de TFS maligno primario.

Palabras clave:
Tumor fibroso solitario
Glándula parótida
Informe de un caso
Revisión

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