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肛管腺癌伴MUC5AC表达,提示起源于肛门腺。

Anal canal adenocarcinoma with MUC5AC expression suggestive of anal gland origin.

作者信息

Kuroda Naoto, Tanida Nobuyuki, Ohara Masahiko, Hirouchi Takashi, Mizuno Keiko, Kubo Ayumi, Lee Gang-Hong

机构信息

Department of Pathology and Laboratory Medicine, Kochi Red Cross Hospital, 2-13-51 Shin-honmachi, Kochi, Kochi 780-8562, Japan.

出版信息

Med Mol Morphol. 2007 Mar;40(1):50-3. doi: 10.1007/s00795-006-0344-5. Epub 2007 Mar 29.

Abstract

Anal canal adenocarcinomas arising in the anal ducts or glands are very rare neoplasms, and few useful immunohistochemical markers of these carcinomas are known to date. A 57-year-old man presented with anal bleeding, difficulty of defecation, and anal pain. Macroscopic findings of the surgically resected material showed circular stenosis of the anal canal. The mucosal surface was generally intact, but focal ulceration was seen. Microscopically, the proliferation of adenocarcinoma cells with mucin production was observed in the submucosal and muscular layers. The special stains of periodic acid-Schiff (PAS) and Alcian blue confirmed the presence of neutral and acid mucin. Immunohistochemically, normal rectal-type mucosa and normal anal ducts/glands showed the patterns of cytokeratin 7 (CK7)(-)/CK19(+, focal)/MUC5AC(-) and CK7(+, diffuse)/CK19(+, diffuse)/MUC5AC(+, focal), respectively, and neoplastic cells showed the pattern of CK7(+, diffuse)/CK19(+, diffuse)/MUC5AC(+, focal). Finally, our preliminary report suggests that the immunohistochemical combination of CK7, CK19, and MUC5AC may be an available marker for adenocarcinoma of anal ducts/glands origin.

摘要

起源于肛管导管或腺体的肛管腺癌是非常罕见的肿瘤,迄今为止,已知的这类癌的有用免疫组化标记物很少。一名57岁男性患者出现肛门出血、排便困难和肛门疼痛。手术切除标本的宏观表现显示肛管呈环形狭窄。黏膜表面大体完整,但可见局灶性溃疡。显微镜下,在黏膜下层和肌层观察到腺癌细胞伴有粘蛋白产生的增殖。过碘酸希夫(PAS)和阿尔辛蓝特殊染色证实存在中性和酸性粘蛋白。免疫组化方面,正常直肠型黏膜和正常肛管/腺体分别显示细胞角蛋白7(CK7)(-)/CK19(+,局灶性)/MUC5AC(-)和CK7(+,弥漫性)/CK19(+,弥漫性)/MUC5AC(+,局灶性)的模式,而肿瘤细胞显示CK7(+,弥漫性)/CK19(+,弥漫性)/MUC5AC(+,局灶性)的模式。最后,我们的初步报告表明,CK7、CK19和MUC5AC的免疫组化组合可能是肛管/腺体起源腺癌的一种可用标记物。

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