Year 2023 / Volume 115 / Number 6
Letter
Perivascular epithelioid cell tumor (PEComa) of the liver. An extremely rare diagnosis

348-349

DOI: 10.17235/reed.2023.9558/2023

Cristóbal Perán Fernández, Ángel de Paco Navaro, Juan Castañer Ramón-Llin, Julia Bertelli Puche, Alberto Sánchez Espinosa,

Abstract
Hepatic PEComa are tumors that show perivascular epithelioid cell differentiation. Scarcely published, its management is based on small case series and currently its treatment of choice is surgical resection. We present a clinical case of a 74-year-old woman who underwent surgery at our hospital for a benign hepatic PEComa.
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References
1. Attard A, Piscopo N, Schembri J, et al. A Rare Case of PEComa of the Liver. GE Port J Gastroenterol. 2021;28(3):217-221.
Domínguez-González M, Coronel Villara MJ, Rubio Garrido J, et al. Tumor de células epitelioides perivasculares en cuerpo uterino asociado a complejo de esclerosis tuberosa en mujer de 18 años. Prog Obstet Ginecol. 2013;56:147–50
Horvat N, Nikolovski I, Long N, et al. Imaging features of hepatocellular carcinoma compared to intrahepatic cholangiocarcinoma and combined tumor on MRI using liver imaging and data system (LI-RADS) version 2014. Abdom Radiol (NY) 2018 Jan;43(1):169–78.
Casali P.G. Histology- and non-histology-driven therapy for treatment of soft tissue sarcomas. Ann. Oncol. 2012;23:x167–x169.
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Perán Fernández C, de Paco Navaro Á, Castañer Ramón-Llin J, Bertelli Puche J, Sánchez Espinosa A. Perivascular epithelioid cell tumor (PEComa) of the liver. An extremely rare diagnosis. 9558/2023


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Publication history

Received: 26/02/2023

Accepted: 24/04/2023

Online First: 26/05/2023

Published: 06/06/2023

Article Online First time: 89 days

Article editing time: 100 days


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