Solitary fibrous tumor of the liver. Case report and review of the literature

Solitary fibrous tumor (SFT) is a rare mesenchymal tumor. Given its origin, it can appear in almost any location. In the literature, only 50 cases of SFT in the liver parenchyma have been reported. Despite its rarity, this entity should be included in the differential diagnosis of liver masses. We r...

Full description

Saved in:
Bibliographic Details
Published inRevista española de enfermedades digestivas Vol. 107; no. 10; pp. 633 - 639
Main Authors Bejarano-González, Natalia, García-Borobia, Francisco Javier, Romaguera-Monzonís, Andreu, García-Monforte, Neus, Falcó-Fagés, Joan, Bella-Cueto, M Rosa, Navarro-Soto, Salvador
Format Journal Article
LanguageEnglish
Published Spain Sociedad Española de Patología Digestiva 01.10.2015
Aran Ediciones
Subjects
Aged
Biopsy
Diagnosis, Differential
Embolización portal
Embolización prequirúrgica
Embolización transarterial
Female
Gastroenterology & Hepatology
Geriatrics & Gerontology
Humans
Infectious Diseases
Liver Neoplasms - diagnostic imaging
Liver Neoplasms - pathology
Liver Neoplasms - surgery
Neoplasia mesenquimal
Oncology
Pathology
Pharmacology & Pharmacy
Radiology, Nuclear Medicine & Medical Imaging
Revisión
Solitary Fibrous Tumors - diagnostic imaging
Solitary Fibrous Tumors - pathology
Solitary Fibrous Tumors - surgery
Surgery
Tomography, X-Ray Computed
Tumor fibroso solitario hepático
Ultrasonography
Portal venous embolization
Embolización prequirúrgica
Mesenchymal neoplasia
Revisión
Pre-surgical embolization
Embolización transarterial
Tumor fibroso solitario hepático
Embolización portal
Transarterial embolization
Review
Neoplasia mesenquimal
Liver solitary fibrous tumor
Online AccessGet full text

Cover

More Information
Summary:Solitary fibrous tumor (SFT) is a rare mesenchymal tumor. Given its origin, it can appear in almost any location. In the literature, only 50 cases of SFT in the liver parenchyma have been reported. Despite its rarity, this entity should be included in the differential diagnosis of liver masses. We report the first case with imaging data from five years prior to diagnosis, which was treated by right portal embolization and arterial tumor embolization, and subsequent liver resection. We also present an exhaustive review of the cases described to date.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:1130-0108
DOI:10.17235/reed.2015.3676/2014