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A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature

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dc.contributor.authorTepeler, Abdulkadir
dc.contributor.authorErdem, Mehmet Remzi
dc.contributor.authorKurt, Omer
dc.contributor.authorTopaktas, Ramazan
dc.contributor.authorKilicaslan, Isin
dc.contributor.authorArmagan, Abdullah
dc.contributor.authorOnol, Sinasi Yavuz
dc.date.accessioned2020-10-29T23:02:01Z
dc.date.available2020-10-29T23:02:01Z
dc.date.issued2011-01-01T00:00:00Z
dc.description.abstractPrimary renal mucinous cystadenocarcinoma is a very rare lesion of kidney which originates from the metaplasia of the renal pelvic uroepithelium. Only one case with primary mucinous cystadenocarcinoma has been reported in the English literature. We report second case of mucinous cystadenocarcinoma which was radiologically classified as type-IIF Bosniak cyst in peripheral localization. We aimed to present this extreme and unusual entity with its radiological, surgical, and pathologic aspects under the light of literature.
dc.identifier.citationTepeler A., Erdem M. R. , Kurt O., Topaktas R., Kilicaslan I., Armagan A., Onol S. Y. , -A Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature-, CASE REPORTS IN MEDICINE, 2011
dc.identifier.doi10.1155/2011/686283
dc.identifier.pubmed22110514
dc.identifier.scopus84877705501
dc.identifier.urihttp://hdl.handle.net/20.500.12645/26839
dc.identifier.wosWOS:000215229900158
dc.titleA Rare Renal Epithelial Tumor: Mucinous Cystadenocarcinoma Case Report and Review of the Literature
dc.typeArticle
dspace.entity.typePublication
local.avesis.idcc4d7f0b-2f06-4e40-a812-3a0186abcdd6
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus
local.publication.isinternational1

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