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无腹膜假黏液瘤情况下的同步性卵巢和阑尾黏液性肿瘤

Synchronous Ovarian and Appendiceal Mucinous Neoplasms in the Absence of Pseudomyxoma Peritonei.

作者信息

Gui Xianyong, Escobar Jorge, Lee Cheng-Han, Duggan Máire A, Köbel Martin

机构信息

*Department of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary; and †Calgary Laboratory Services, Calgary; and ‡Department of Pathology, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Int J Gynecol Cancer. 2017 Feb;27(2):214-222. doi: 10.1097/IGC.0000000000000871.

DOI:10.1097/IGC.0000000000000871
PMID:27870702
Abstract

BACKGROUND

Synchronous ovarian/appendiceal mucinous neoplasms sometimes occur in the absence of clinical pseudomyxoma peritonei (PMP), which raises a question about whether the 2 tumors could be independent.

METHODS

We identified 11 cases of synchronous ovarian/appendiceal mucinous neoplasms without PMP and subclassified them into groups 1 and 2 based on the presence or absence of microscopic peritoneal/ovarian surface mucin deposits. A 7-marker panel (CK7, CK20, CDX2, PAX8, MUC1, MUC2, and MUC5AC) immunohistochemistry was performed on both tumors.

RESULTS

Between the 2 groups, there were no significant differences in age, laterality, size, and histology of ovarian/appendiceal tumors. In group 1, 2 of 4 cases developed PMP later, and both had ovarian surface and contralateral ovarian involvement and appendiceal perforation with microscopic mucin deposits on the peritoneum. No patients in group 2 developed PMP. All group 1 cases showed a high degree of concordance of immunoprofile between the synchronous tumors, with an identical expression of appendiceal pattern in greater than 90% of the markers. In group 2, only 1 of 7 cases showed concordance in all markers.

CONCLUSIONS

If peritoneal mucin deposits present, even microscopic and acellular, the synchronous tumors are most likely of a single appendiceal origin. Otherwise, they are more heterogeneous, and some may be truly dual primaries.

摘要

背景

同步性卵巢/阑尾黏液性肿瘤有时在无临床腹膜假黏液瘤(PMP)的情况下发生,这引发了关于这两种肿瘤是否可能独立存在的疑问。

方法

我们确定了11例无PMP的同步性卵巢/阑尾黏液性肿瘤病例,并根据有无显微镜下腹膜/卵巢表面黏液沉积将其分为1组和2组。对两种肿瘤均进行了7标志物免疫组化检测(CK7、CK20、CDX2、PAX8、MUC1、MUC2和MUC5AC)。

结果

两组之间,卵巢/阑尾肿瘤的年龄、双侧性、大小和组织学无显著差异。在1组中,4例中有2例后来发生了PMP,两者均有卵巢表面和对侧卵巢受累以及阑尾穿孔,腹膜有显微镜下黏液沉积。2组中无患者发生PMP。1组所有病例的同步性肿瘤之间免疫表型高度一致,超过90%的标志物呈现阑尾型相同表达。在2组中,7例中只有1例所有标志物一致。

结论

如果存在腹膜黏液沉积,即使是显微镜下的和无细胞的,同步性肿瘤很可能起源于单一阑尾。否则,它们更具异质性,有些可能是真正的双原发肿瘤。

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