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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/11456
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dc.contributor.authorButnari, Valentin-
dc.contributor.authorSchiopu, Victor-
dc.date.accessioned2020-08-21T13:32:38Z-
dc.date.available2020-08-21T13:32:38Z-
dc.date.issued2018-
dc.identifier.citationBUTNARI, Valentin, SCHIOPU, Victor. Primary retroperitoneal liposarcoma. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 115.en_US
dc.identifier.urihttps://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf-
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/11456-
dc.descriptionNicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldovaen_US
dc.description.abstractIntroduction. Liposarcoma is a common type of soft tissue sarcoma, which occurs most commonly in the extremities (52%), followed by the retroperitoneum (19%). Retroperitoneal liposarcoma (RL) is usually asymptomatic until the liposarcoma is large enough to compress the surrounding organs. It is often misdiagnosed due to its rarity and absence of symptoms. The symptoms of the tumor would not arise until the tumor grows to a certain dimension. Presence of a palpable abdominal mass is the main symptom at diagnosis. The management is surgical intervention. Even with complete removal of the liposarcoma, prognosis remains poor.en_US
dc.language.isoenen_US
dc.publisherMedEsperaen_US
dc.subjectPrimary Retroperitoneal Tumor (PRT)en_US
dc.subjectretroperitoneal space (RS)en_US
dc.subjectRetroperitoneal liposarcoma (RL)en_US
dc.titlePrimary retroperitoneal liposarcomaen_US
dc.typeArticleen_US
Appears in Collections:MedEspera 2018

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