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

Abdülkadir Tepeler | Zendy; Mehmet Remzi Erdem | Zendy; Ömer Kurt | Zendy; Ramazan Topaktaş | Zendy; İşın Kiliçaslan | Zendy; Abdullah Armağan | Zendy; Şinasi Yavuz Önol | Zendy

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

Author(s) -

Abdülkadir Tepeler,

Mehmet Remzi Erdem,

Ömer Kurt,

Ramazan Topaktaş,

İşın Kiliçaslan,

Abdullah Armağan,

Şinasi Yavuz Önol

Publication year - 2011

Publication title -

case reports in medicine

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.2

H-Index - 20

eISSN - 1687-9627

pISSN - 1687-9635

DOI - 10.1155/2011/686283

Subject(s) - mucinous cystadenocarcinoma , medicine , cystadenocarcinoma , pathology , cyst , radiology , adenocarcinoma , cancer , ovary

Primary 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.

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