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宫颈不典型类癌伴原位腺癌。

Atypical carcinoid of the uterine cervix accompanying adenocarcinoma in situ.

机构信息

Department of Gynecology and Obstetrics, West China Second Hospital, Sichuan University, Chengdu, People's Republic of China.

West China School of Medicine, Sichuan University, Chengdu, People's Republic of China.

出版信息

J Clin Pathol. 2018 Nov;71(11):1030. doi: 10.1136/jclinpath-2018-205081. Epub 2018 Aug 28.

DOI:10.1136/jclinpath-2018-205081
PMID:30154130
Abstract

CLINICAL QUESTION

A 45-year-old woman presented with painless vaginal bleeding for 2 months. A biopsy was taken from the uterine cervix, and poorly differentiated adenocarcinoma was suspected. After three cycles of neoadjuvant chemotherapy treatment, the patient underwent radical hysterectomy with bilateral salpingo-oophorectomy, and pelvic and para-aortic lymphadenectomy.Review the high quality, interactive digital Aperio slide at http://virtualacp.com/JCPCases/jclinpath-2018-205081-1/ and consider your diagnosis. WHAT IS YOUR DIAGNOSIS?: Typical carcinoid.Poorly differentiated adenocarcinoma.Atypical carcinoid.Small cell neuroendocrine carcinoma.Sex cord-stromal tumours of the uterine cervix.-The correct answer is after the discussion.

DISCUSSION

Neuroendocrine tumours of the uterine cervix are a rare cancer of the female reproductive system, accounting for approximately 1% of all female cervical malignancies.1 2 In 1997, a consensus workshop suggested four types of neuroendocrine tumours of the uterine cervix: typical and atypical carcinoid tumours, small cell neuroendocrine carcinomas, and large cell carcinomas.1 Among all the categories, small cell neuroendocrine carcinomas are of the highest incidence. A PubMed search revealed that only 15 cases of atypical carcinoid tumours of the uterine cervix have been reported.3 4 Because of infrequency, the clinical and pathological features of atypical carcinoid tumours of the uterine cervix remain unknown.Atypical carcinoids are characterised by great cytological atypia, which means abundant or scanty cytoplasm and visible nucleoli with granular chromatin. Tumour cells lined up in insular, trabecular, columnar and nested organoid patterns; they are epithelioid in appearance, but can be spindled (figure 1A). Necrosis could be observed in some areas and mitotic activity is up to 10 mitotic figures/10 high-power field (figure 1B). On immunohistochemistry, atypical carcinoids are diffuse and positive for Syn, CgA and CD56 (figure 2). An electron microscopic test was done, and several neuroendocrine granules were distributed in the tumour cell plasma (figure 3).jclinpath;71/11/1030/F1F1F1Figure 1(A) Insular, trabecular and columnar patterns of tumour cells were focally observed in the deep stroma of the cervix (H&E ×200). (B) Tumour cells showed small-sized, scanty cytoplasm, enlarged and deeply stained nuclei with condensed chromatin, obvious atypia, and increased mitotic activity (H&E ×400). (C) The cervical gland has shown atypical hyperplasia and adenocarcinoma in situ (H&E ×200).jclinpath;71/11/1030/F2F2F2Figure 2Immunohistochemical study findings: (A-C) The neuroendocrine markers Syn, CgA and CD56 were diffuse with strong expression in the tumour cell plasma. (D-E) P63 and CK5/6 for the squamous cell carcinomas showed no expression. (F-G) P16 for atypical carcinoid and adenocarcinoma in situ, respectively, had strong diffuse expression. (H-I) Ki67 had low expression in both atypical carcinoid and adenocarcinoma in situ (×200).jclinpath;71/11/1030/F3F3F3Figure 3Several neuroendocrine granules were distributed in the tumour cell plasma.Neuroendocrine tumours of the uterine cervix are sometimes combined with adenocarcinoma (figure 1C); their cytological and immunohistochemical features showed the neuroendocrine and adenomatous components shared the same origin.

摘要

临床问题

一位 45 岁女性出现无痛性阴道出血 2 个月。宫颈活检怀疑为低分化腺癌。行新辅助化疗 3 周期后,行根治性子宫切除术+双侧附件切除术+盆腔和腹主动脉旁淋巴结清扫术。请浏览高质量、交互式的 Aperio 数字切片 http://virtualacp.com/JCPCases/jclinpath-2018-205081-1/,并考虑诊断。

你的诊断是什么?

典型类癌。

低分化腺癌。

不典型类癌。

小细胞神经内分泌癌。

宫颈性索-间质肿瘤。

-答案在讨论后给出。

讨论

宫颈神经内分泌肿瘤是一种罕见的女性生殖系统癌症,约占所有女性宫颈癌的 1%。1997 年,一个共识研讨会建议将宫颈神经内分泌肿瘤分为 4 种类型:典型和不典型类癌、小细胞神经内分泌癌和大细胞癌。1 在所有类别中,小细胞神经内分泌癌的发病率最高。在 PubMed 上进行检索,仅发现 15 例宫颈不典型类癌的病例报告。3,4 由于罕见,宫颈不典型类癌的临床和病理特征仍不清楚。不典型类癌的特点是细胞异型性明显,即细胞质丰富或稀少,核仁可见,染色质颗粒状。肿瘤细胞排列呈岛状、小梁状、柱状和巢状;外观呈上皮样,但也可以呈梭形(图 1A)。部分区域可见坏死,有丝分裂活性高达 10 个有丝分裂/10 高倍视野(图 1B)。免疫组化染色显示,不典型类癌弥漫性表达 Syn、CgA 和 CD56(图 2)。进行电镜检查,发现肿瘤细胞浆内分布有几个神经内分泌颗粒(图 3)。

宫颈神经内分泌肿瘤有时与腺癌并存(图 1C);其细胞学和免疫组化特征表明神经内分泌和腺癌成分具有相同的起源。

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