Title Primary mesenchymal chondrosarcoma with bilateral kidney invasion and calcification in renal pelvis: A case report and review of the literature
Authors Chen, Duqun
Ye, Zi
Wu, Xionghui
Shi, Bentao
Zhou, Lijun
Sun, Shuolei
Wei, Benlin
Yang, Shangqi
Mao, Xiangming
Lai, Yongqing
Affiliation Peking Univ, Shenzhen Hosp, Dept Urol, Shenzhen 518036, Guangdong, Peoples R China.
Peking Univ, Shenzhen Hosp, Guangdong & Shenzhen Key Lab Male Reprod Med & Ge, Inst Urol,Shenzhen PKU HKUST Med Ctr, Shenzhen 518036, Guangdong, Peoples R China.
Anhui Med Univ, Affiliated Hosp 1, Dept Infect Dis, Hefei 230032, Anhui, Peoples R China.
Peking Univ, Shenzhen Hosp, Dept Urol, 1120 Lianhua Rd, Shenzhen 518036, Guangdong, Peoples R China.
Keywords mesenchymal chondrosarcoma
bilateral kidney invasion
calcification
renal pelvis
Issue Date 2015
Publisher ONCOLOGY LETTERS
Citation ONCOLOGY LETTERS.2015,10,(2),1075-1078.
Abstract Mesenchymal chondrosarcoma (MC) is a rare malignant cartilaginous forming tumor. MC of the kidney is extremely rare, with only seven cases reported in the literature. The present study described the case of a 17-year-old male, who presented with sudden severe pain in the right flank and a high fever. Imaging studies demonstrated a large soft heterogeneous mass (7.8x9.5x15 cm) located between the liver and right kidney with no clear demarcation, and a well-demarcated mass (1.3x2.4 cm) with patchy dense calcification occupying the left renal pelvis. Following the diagnosis of a Wilms' tumor, the patient underwent a right radical nephrectomy and the pathological diagnosis was MC of the kidney. To the best of our knowledge, the current study presents the first case of MC with bilateral kidney invasion and calcification in the renal pelvis. In addition, the clinical, radiological and pathological features, and the management of this unusual neoplasm were discussed.
URI http://hdl.handle.net/20.500.11897/417784
ISSN 1792-1074
DOI 10.3892/ol.2015.3252
Indexed SCI(E)
PubMed
Appears in Collections: 深圳医院

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