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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/13071
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dc.contributor.authorGuțu, E.
dc.contributor.authorMișin, I.
dc.contributor.authorGagauz, I.
dc.date.accessioned2020-11-19T08:40:54Z
dc.date.available2020-11-19T08:40:54Z
dc.date.issued2016
dc.identifier.citationGUȚU, E., MIȘIN, I., GAGAUZ, I. Chistadenom mucinos retroperitoneal primar = Primary retroperitoneal mucinous cystadenoma. In: Arta Medica. 2016, nr. 3(60), p. 101. ISSN 1810-1852.en_US
dc.identifier.issn1810-1852
dc.identifier.urihttps://artamedica.md/old_issues/ArtaMedica_60.pdf
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/13071
dc.descriptionCatedra de chirurgie nr. 1 „Nicolae Anestiadi”, Laboratorul de chirurgie hepato-pancreato-biliară, USMF „Nicolae Testemițanu”, Chişinău, Republica Moldova, Conferința stiințifică „Nicolae Anestiadi – nume etern al chirurgiei basarabene” consacrată centenarului de la nașterea profesorului Nicolae Anestiadi 26 august 2016en_US
dc.description.abstractIntroducere. Chistadenomul mucinos retroperitoneal este o tumoare extrem de rară, diagnosticată doar la femei. Material şi metodă. Autorii prezintă un caz clinic de chistadenom mucinos retroperitoneal confirmat histopatologic la o pacientă de 41 ani. Tomografia computerizată a pus în evidenţă o tumoră chistică de 21×16 cm cu localizare retroperitoneală dreaptă. Rezultate. S-a practicat excizia tumorii fără alte proceduri adiţionale, iar examenul histologic a confirmat chistadenom mucinos. Examenul histologic a sugerat că tumora are origine în mezoteliul celomic cu metaplazie mucinoasă. Concluzie. Sunt prezentate particularităţile clinicopatologice, modalitatea de diagnostic, opţiunile terapeutice şi rezultatul tratamentului prin prisma cazurilor clinica publicate în literatura de specialitate.en_US
dc.description.abstractIntroduction. Retroperitoneal mucinous cystadenomas are extremely rare tumors found exclusively in women. Material & methods. An additional case of retroperitoneal mucinous cystadenoma histological confirmed in a 41-year-old woman is reported herein. Computed tomography (CT) scanning showed a cystic mass, 21×16 cm in size, in the right retroperitoneal space. Results. Removal of the cystic tumor was performed without any other additional procedures, and further histological diagnosis was confirmed as primary mucinous cystadenoma of borderline type. Histological findings suggested that the tumor developed from mucinous metaplasia of the coelomic mesothelium. Conclusion. Clinicopathological features, diagnostic findings, therapeutic options and the outcome are analyzed in this paper having reviewed the cases reported in world literature.
dc.publisherAsociaţia chirurgilor “Nicolae Anestiadi” din Republica Moldovaen_US
dc.subjectmucinous cystadenomaen_US
dc.subjectretroperitoneal tumoren_US
dc.titleChistadenom mucinos retroperitoneal primaren_US
dc.title.alternativePrimary retroperitoneal mucinous cystadenomaen_US
dc.typeOtheren_US
Appears in Collections:Arta Medica Vol. 60, No 3, 2016 ediție specială

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