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子宫内膜原发性黏液腺癌。一项临床病理与组织化学研究。

Primary mucinous adenocarcinoma of the endometrium. A clinicopathologic and histochemical study.

作者信息

Ross J C, Eifel P J, Cox R S, Kempson R L, Hendrickson M R

出版信息

Am J Surg Pathol. 1983 Dec;7(8):715-29.

PMID:6318581
Abstract

Of 256 patients with carcinoma confined to the uterine corpus at the time of hysterectomy treated in the period 1959-1975 at Stanford University Hospital, 98 patients (38%) had neoplasms which demonstrated at least focal intracytoplasmic mucin. In 21 carcinomas (9%), intracytoplasmic mucin production was the dominant form of differentiation--a group which we designate primary mucinous carcinoma of the endometrium. Freedom from relapse and frequency of myometrial invasion were not statistically different for patients whose neoplasms contained intracytoplasmic mucin, regardless of the amount of mucin present, when compared with cases of nonmucin-containing carcinoma. Using histochemical methods, it was impossible reliably to distinguish between the intracytoplasmic mucin produced by carcinomas arising in endometrium and that produced by carcinomas primary in the endocervix. Differential biopsy and fractional curettage are stressed as useful tools in making this clinically important distinction. Since both benign mucinous metaplasia and mucinous carcinoma may arise in the endometrium, it is important to establish histopathologic criteria by which the malignant lesions may be recognized. The use of criteria illustrated in this paper (which include architectural complexity of proliferation, epithelial stratification, loss of epithelial polarity, and nuclear atypicality) resulted in the recognition of mucin producing proliferations which as a group manifest a 50% incidence of myometrial invasion.

摘要

1959年至1975年期间在斯坦福大学医院接受子宫切除术治疗的256例子宫体局限型癌患者中,98例(38%)肿瘤至少有局灶性胞浆内黏液。在21例癌(9%)中,胞浆内黏液分泌是主要的分化形式——我们将这一组称为子宫内膜原发性黏液癌。与不含黏液的癌病例相比,肿瘤含有胞浆内黏液的患者,无论黏液量多少,其复发率和肌层浸润频率在统计学上无差异。使用组织化学方法,无法可靠地区分子宫内膜癌产生的胞浆内黏液和宫颈原发性癌产生的胞浆内黏液。强调鉴别活检和分段刮宫是做出这一临床重要区分的有用工具。由于良性黏液化生和黏液癌均可发生于子宫内膜,因此建立可识别恶性病变的组织病理学标准很重要。使用本文所示的标准(包括增殖的结构复杂性、上皮分层、上皮极性丧失和核异型性)可识别出产生黏液的增殖,这一组增殖表现出50%的肌层浸润发生率。

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