| Literature DB >> 28123739 |
Jing Quan1, Xiang Pan1, Lu Jin1, Tao He2, Jia Hu2, Bentao Shi3, Jian Peng3, Zhebo Chen3, Shangqi Yang3, Xiangming Mao3, Yongqing Lai3.
Abstract
Urachal carcinoma is a rare tumor that most commonly occurs in ovaries and less often in the adnexal region and urinary system. We herein present two cases of urachal carcinoma: One case was a 32-year-old male patient who presented with painless hematuria with blood clots for 1 month, whereas the other case was a 50-year-old woman who presented with gross hematuria with mild dysuria, urgency and frequent urination for 1 year. Following surgical resection, the two patients were diagnosed with urachal adenocarcinoma (mixed type) and urachal mucinous adenocarcinoma, respectively, based on the histopathological examination. A review of previously published cases and relevant literature is also presented. The aim of the present study was to help understand this disease better, in order to reduce the rate of clinical and pathological misdiagnosis.Entities:
Keywords: computed tomography; urachal carcinoma; urachal mucinous carcinoma
Year: 2016 PMID: 28123739 PMCID: PMC5244972 DOI: 10.3892/mco.2016.1082
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450