Taniguchi S, Yamanari H, Inada K, Iwamura T, Hokkoku S, Tanaka S, Fukuda M, Setoguchi T
First Department of Surgery, Miyazaki Medical College, Japan.
Surg Today. 1996;26(9):707-10. doi: 10.1007/BF00312089.
Adenocarcinoma in the anal canal associated with an anal fistula is extremely rare, and in most cases its origin is difficult to ascertain because the primary sites have already been destroyed before any diagnosis of malignancy is able to be made. We report herein the case of a 62-year-old man found to have papillary adenocarcinoma with partial mucinous carcinoma associated with an anal fistula. The tumor was not exposed to the mucosal surface of the anal canal or rectum and an abdominoperineal resection was carried out. Macroscopic findings suggested that the tumor had developed from the anal fistula; however, the tumor showed a positive results when tested for O-acetylated sialic acids. This test also proved positive in the mucus of normal rectal mucosa, but not in the mucus of the anal glands. We speculated that the results of these tests may indicate that this tumor could have originated from the rectal mucosa, from where it migrated into the anal fistula.
肛管腺癌合并肛瘘极为罕见,在大多数情况下,由于在做出任何恶性肿瘤诊断之前原发部位就已被破坏,其起源难以确定。我们在此报告一例62岁男性,发现患有伴有肛瘘的乳头状腺癌伴部分黏液腺癌。肿瘤未暴露于肛管或直肠的黏膜表面,遂行腹会阴联合切除术。宏观检查结果提示肿瘤由肛瘘发展而来;然而,该肿瘤在检测O-乙酰化唾液酸时呈阳性。此检测在正常直肠黏膜黏液中也呈阳性,但在肛门腺黏液中则为阴性。我们推测这些检测结果可能表明该肿瘤可能起源于直肠黏膜,然后迁移至肛瘘。