Department of General Surgical Science (Surgery I), Graduate School of Medicine, Gunma University, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.
Surg Today. 2012 Jul;42(7):697-702. doi: 10.1007/s00595-012-0178-9. Epub 2012 Apr 7.
Extramammary Paget's disease (EPD) is rare. We report a case of double anal canal cancers in a patient with a long history of perianal Paget's disease. The patient, a 68-year-old Japanese woman, refused surgery initially and was treated with electron beam therapy, which achieved remission. However, 6 years later, Paget's disease was found to be progressing again and double anal canal tumors were also detected in the proctos and external skin area. We performed abdominoperineal resection (Miles' operation) and lymph node dissection for the Paget's disease with double anal canal tumors. Immunohistochemical staining revealed cytokeratin (CK)-20 expression in the adenocarcinomas and Paget's disease lesion, but not CK-7 or gross cystic disease fluid protein-15 expression. The lesion was joined to the carcinoma by a stalk. The immunohistochemistry results suggested secondary EPD, although it was originally considered to be Paget's carcinoma (primary EPD) based on the clinical history.
派杰氏病(EPD)罕见。我们报告了一例长期肛周派杰氏病患者的双肛管癌。该患者为 68 岁日本女性,最初拒绝手术,接受电子束治疗后获得缓解。然而,6 年后,派杰氏病再次进展,且直肠和外部皮肤区域均发现双肛管肿瘤。我们对双肛管肿瘤伴派杰氏病进行腹会阴切除术(Miles 手术)和淋巴结清扫术。免疫组织化学染色显示腺癌和派杰氏病病变中 CK-20 表达,而 CK-7 或大囊性病液蛋白 15 不表达。病变通过蒂与癌相连。免疫组化结果提示为继发性 EPD,尽管根据临床病史最初认为是派杰氏癌(原发性 EPD)。