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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/11455
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dc.contributor.authorSchiopu, Victor-
dc.date.accessioned2020-08-21T13:28:28Z-
dc.date.available2020-08-21T13:28:28Z-
dc.date.issued2018-
dc.identifier.citationSCHIOPU, Victor. The neurogenic retroperitoneal primitive tumors. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 114-115.en_US
dc.identifier.urihttps://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf-
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/11455-
dc.descriptionNicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldovaen_US
dc.description.abstractIntroduction. The histological ambiguity of the retroperitoneal space is the cause of the large specter of primitive tumors. Primitive tumors are classified in those with a mesodermal origin, neurogenic, vestigial, retroperitoneal cysts and various tumors. The neurogenic tumors may have different origins: ganglion cell (ganglioneuromas, ganglioneuroblastomas, neuroblastomas), paraganglionic system (paragangliomas, pheochromocytomas) and nerve sheath (schwannomas, neurofibromas, malignant schwannomas). The neurogenic primitives tumors usually present late symptoms or become palpable once they have reached a significant size (>10cm). The medical imaging (USG, CT, IRM) does not distinguish benign and malign tumors, and it does not reveal the histological origin. The biopsy and the histological examination of the removed tumor remain the main diagnostic methods.en_US
dc.language.isoenen_US
dc.publisherMedEsperaen_US
dc.subjectPrimary Retroperitoneal Tumor (PRT)en_US
dc.subjectretroperitoneal space (RS)en_US
dc.subjectneurogenic tumoren_US
dc.titleThe neurogenic retroperitoneal primitive tumorsen_US
dc.typeArticleen_US
Appears in Collections:MedEspera 2018

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