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dc.contributor.author Schiopu, Victor
dc.date.accessioned 2020-08-21T13:28:28Z
dc.date.available 2020-08-21T13:28:28Z
dc.date.issued 2018
dc.identifier.citation SCHIOPU, 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.uri https://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/11455
dc.description Nicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldova en_US
dc.description.abstract Introduction. 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.iso en en_US
dc.publisher MedEspera en_US
dc.subject Primary Retroperitoneal Tumor (PRT) en_US
dc.subject retroperitoneal space (RS) en_US
dc.subject neurogenic tumor en_US
dc.title The neurogenic retroperitoneal primitive tumors en_US
dc.type Article en_US


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  • MedEspera 2018
    The 7th International Medical Congress for Students and Young Doctors, May 3-5, 2018

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