Year 2022 / Volume 114 / Number 12
Letter
Intra-abdominal epithelioid angiosarcoma

744-745

DOI: 10.17235/reed.2022.8878/2022

Manuel José Torres Jurado, Jaime López Sánchez, José Edecio Quiñones Sampedro, Luis Muñoz Bellvís,

Abstract
The epithelioid angiosarcoma is a type of sarcoma is very rare (<1 % of all sarcomas). The most frequent location is in extremities, therefore is the axial region less common.Differential diagnosis with other histologic variants of intra-abdominal hepatic and splenic angiosarcomas is essential. Surgery is the treatment of choice, and there is no current evidence on the management of cases with locoregional or distant involvement.
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References
1. Noujaim J, Thway K, Bajwa Z, et al. Epithelioid Sarcoma: Opportunities for Biology-Driven Targeted Therapy. Front Oncol. 2015; 17(5):186.
2. Thway K, Jones RL, Noujaim J, et al. Epithelioid Sarcoma: Diagnostic Features and Genetics. Adv Anat Pathol. 2016;23(1):41-9.
3. Sparber-Sauer M, Koscielniak E, Vokuhl C, et al. Epithelioid sarcoma in children, adolescents, and young adults: Localized, primary metastatic and relapsed disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry. Pediatr Blood Cancer. 2019;66(9): e27879.
4. Alvite M, Alonso L, Seoane M, et al. Angiosarcoma primario de bazo. Rev Esp Enferm Dig. 2008; 100 (6): 373-9.
5. Bernardos L, García A, Rey C. Angiosarcoma hepático. Rev Esp Enferm Dig. 2008; 100 (12): 804-6.
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Torres Jurado M, López Sánchez J, Quiñones Sampedro J, Muñoz Bellvís L. Intra-abdominal epithelioid angiosarcoma . 8878/2022


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Publication history

Received: 20/04/2022

Accepted: 30/04/2022

Online First: 24/05/2022

Published: 12/12/2022

Article Online First time: 34 days

Article editing time: 236 days


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