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肛管黏膜腺泡细胞腺癌伴肛周派杰病:一例罕见病例报告并文献复习

Goblet cell adenocarcinoma of the anal canal with perianal Paget disease: A rare case report with literature review.

机构信息

Department of Pathology, Shaoxing People's Hospital, Shaoxing, Zhejiang, China.

出版信息

Medicine (Baltimore). 2023 Apr 21;102(16):e33598. doi: 10.1097/MD.0000000000033598.

Abstract

INTRODUCTION

AS an uncommon neoplasm, goblet cell adenocarcinoma (GCA) is characterized by mixed endocrine-exocrine features. It is almost exclusively found in the appendix. Primary GCA of the anal canal is extremely rare.

CASE PRESENTATION

Herein we describe a novel rare case of 74-year-old Chinese female who is diagnosed with GCA in the anal canal with perianal Paget disease, including a brief review of the literature. In the lesion of anal canal, the tumor was composed of signet-ring-like cells on confluent growth model and copious mucin was produced as well. Simultaneously, the results of immunohistochemistry showed signet-ring-like cells were positive for CK20, CDX2, synaptophysin (Syn), CD56, carcinoembryonic antigen (CEA) and Villin. Meanwhile, the Ki67-labeling index reached 40%. In the lesion of perianal Paget disease, the small groups of atypical neoplastic cells were present in the epidermis. Immunohistochemically, the neoplastic cells were positive for CK20, CDX2 and epithelial membrane antigen, but negative for CK7, GCDFP15, S100, HMB45, and P63. The Ki67-labeling index reached 60% in the most concentrated spot.

CONCLUSIONS

Extra-appendiceal GCA was rare and easily under-recognizable. The diagnosis of GCA was seldom made preoperatively. Occasionally, GCA could occur in the anal canal accompanied by perianal Paget disease. So careful rectal examination was important in the patient with perianal Paget disease for avoid missing diagnosis of GCA on anal canal. GCA may show aggressive clinical behavior compared with typical well-differentiated neuroendocrine tumors. Therefore, we should pay more attention on the recognization of this rare disease.

摘要

简介

作为一种罕见的肿瘤,杯状细胞腺癌(GCA)的特点是混合内分泌-外分泌特征。它几乎只发生在阑尾。肛门管的原发性 GCA 极为罕见。

病例介绍

本文描述了一例 74 岁中国女性罕见病例,该患者被诊断为肛门管 GCA 伴肛周派杰病,同时对文献进行了简要回顾。在肛门管病变中,肿瘤呈融合生长模式的印戒样细胞,大量产生粘蛋白。同时,免疫组化结果显示印戒样细胞 CK20、CDX2、突触素(Syn)、CD56、癌胚抗原(CEA)和微管相关蛋白(Villin)阳性。同时,Ki67 标记指数达到 40%。在肛周派杰病病变中,表皮存在小群异型肿瘤细胞。免疫组化显示,肿瘤细胞 CK20、CDX2 和上皮膜抗原阳性,CK7、GCDFP15、S100、HMB45 和 P63 阴性。最密集点的 Ki67 标记指数达到 60%。

结论

阑尾外 GCA 罕见,易被误诊。术前很少能做出 GCA 的诊断。偶尔,GCA 可发生在肛门管伴肛周派杰病。因此,对于肛周派杰病患者,仔细进行直肠检查非常重要,以避免遗漏肛门管 GCA 的诊断。与典型的高分化神经内分泌肿瘤相比,GCA 可能表现出更具侵袭性的临床行为。因此,我们应该更加注意这种罕见疾病的识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f577/10118358/2564992f3fc4/medi-102-e33598-g001.jpg

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