Perivascular epithelioid cell tumor of the rectum: report of a case and review of the literature

被引:12
作者
Kanazawa, Amane [1 ]
Fujii, Shoichi [1 ]
Godai, Ten-i [1 ]
Ishibe, Atsushi [1 ]
Oshima, Takashi [1 ]
Fukushima, Tadao [1 ]
Ota, Mitsuyoshi [1 ]
Yukawa, Norio [2 ]
Rino, Yasushi [2 ]
Imada, Toshio [2 ]
Ito, Junko [3 ]
Nozawa, Akinori [3 ]
Masuda, Munetaka [2 ]
Kunisaki, Chikara [1 ]
机构
[1] Yokohama City Univ, Med Ctr, Gastroenterol Ctr, Minami Ku, Yokohama, Kanagawa 2320024, Japan
[2] Yokohama City Univ, Dept Surg, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[3] Yokohama City Univ, Med Ctr, Dept Pathol, Minami Ku, Yokohama, Kanagawa 2320024, Japan
关键词
Perivascular epithelioid cell tumor; PEComa; Transanal endoscopic microsurgery; SARCOMA MALIGNANT PECOMA; GASTROINTESTINAL-TRACT; SUGAR TUMOR; COLON; MEMBER; FAMILY; CHILD;
D O I
10.1186/1477-7819-12-12
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We report a case of perivascular epithelioid cell tumor arising in the rectum of a 55-year-old woman. The tumor was treated by transanal endoscopic microsurgery. After 1 year follow-up, the patient is alive with no radiologic or endoscopic evidence of recurrence. Perivascular epithelioid cell tumor is a rare mesenchymal tumor characterized by co-expression of melanocytic and smooth muscle markers. This rare tumor can arise in various organs, including the falciform ligament, uterus, uterine cervix, liver, kidney, lung, breast, cardiac septum, pancreas, prostate, thigh, and gastrointestinal tract. Perivascular epithelioid cell tumor of the gastrointestinal tract is very rare, with only 23 previously reported cases. We review the literature on perivascular epithelioid cell tumors arising in the gastrointestinal tract.
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页数:6
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