Renal medullary carcinoma in a young mixed-race man in Japan

被引:3
|
作者
Toriyama, Akane [1 ,2 ]
Izumi, Hiroshi [1 ,3 ]
Tomita, Shigeki [1 ,2 ]
Nagashima, Yoji [4 ]
Ueda, Yoshihiko [5 ]
Aoki, Yusuke [6 ]
Tsujimura, Akira [6 ]
Yao, Takashi [3 ]
Hino, Okio [2 ]
机构
[1] Juntendo Univ, Urayasu Hosp, Dept Pathol, Chiba, Japan
[2] Juntendo Univ, Sch Med, Dept Pathol & Oncol, Bunkyo Ku, Tokyo, Japan
[3] Juntendo Univ, Sch Med, Dept Human Pathol, Bunkyo Ku, Tokyo, Japan
[4] Tokyo Womens Med Univ Hosp, Dept Surg Pathol, Shinjuku Ku, Tokyo, Japan
[5] DOKKYO Med Univ, Saitama Med Ctr, Dept Pathol, Koshigaya, Saitama, Japan
[6] Juntendo Univ, Urayasu Hosp, Dept Urol, Chiba, Japan
基金
日本学术振兴会;
关键词
carcinoma; kidney; medullary; sickle cell trait; COLLECTING DUCT CARCINOMA; CELL-CARCINOMA; PAX8; EXPRESSION; DIAGNOSIS; ANTIBODY; TUMORS;
D O I
10.1111/pin.12783
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Renal medullary carcinoma (RMC) is a rare and aggressive cancer associated with the sickle cell trait. The diagnosis of RMC depends on recognition of its histologic features and immunohistochemical deficiency of INI1, but correct diagnosis is sometimes difficult, especially if a patient's information on race, past, and family medical history is unclear. At present, this is the first report on RMC in Japan.
引用
收藏
页码:241 / 245
页数:5
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