Rutgers Joanne K L, Lawrence W Dwayne
Department of Pathology and Laboratory Medicine (J.K.L.R.), Cedars-Sinai Medical Center, Los Angeles, California Department of Pathology and Laboratory Medicine (W.D.L.), Women and Infants Hospital of Rhode Island, Providence, Rhode Island.
Int J Gynecol Pathol. 2014 Jul;33(4):385-92. doi: 10.1097/PGP.0000000000000143.
In this paper we consider a number of non-neoplastic and neoplastic lesions of the fallopian tube. Emphasis has been placed on diagnostically difficult entities, some of which result in misdiagnosis and consequent alteration of treatment, including "pseudocarcinomas" that represent a florid epithelial response to acute and/or chronic salpingitis. Endometriosis-related lesions may cause infertility, or undergo malignant transformation to a Mullerian carcinoma, most frequently endometrioid and clear cell types. Pregnancy-related tubal lesions include the easily misdiagnosed metaplastic papillary tumor as well as several manifestations of ectopic pregnancy. Covered briefly are familial conditions such as the Peutz-Jeghers syndrome and its association with tubal mucinous metaplasia, clear cell papillary cystadenoma associated with von Hippel-Lindau syndrome, and the Li Fraumeni syndrome's germline p53 mutation and its association with distal tubal p53 signatures. Miscellaneous tumors discussed include the common adenomatoid tumor and the uncommon female adnexal tumor of probable Wolffian origin. Important issues including the updated staging of fallopian tube carcinomas, and the histopathologic variants of endometrioid carcinomas and their sometimes unusual patterns that engender the potential for confusion with other tumors are briefly noted. The final section covers the relatively recent and novel concept of the fallopian tube as the predominant site of origin of ovarian and peritoneal carcinomas. Discussed are the histologic, immunohistochemical, and molecular biologic evidence that support the tubal fimbria as the site of serous tubal intraepithelial carcinoma, possibly the immediate precursor to high-grade ovarian and peritoneal serous carcinoma.
在本文中,我们探讨了输卵管的一些非肿瘤性和肿瘤性病变。重点关注了诊断困难的实体,其中一些会导致误诊并进而改变治疗方案,包括代表对急性和/或慢性输卵管炎的一种旺盛上皮反应的“假癌”。与子宫内膜异位症相关的病变可能导致不孕,或发生恶性转化为苗勒管癌,最常见的是子宫内膜样癌和透明细胞癌。与妊娠相关的输卵管病变包括容易误诊的化生乳头瘤以及异位妊娠的几种表现。简要介绍了一些家族性疾病,如黑斑息肉综合征及其与输卵管黏液化生的关联、与冯·希佩尔 - 林道综合征相关的透明细胞乳头状囊腺瘤,以及李 - 弗劳梅尼综合征的种系p53突变及其与远端输卵管p53特征的关联。讨论的其他肿瘤包括常见的腺瘤样瘤和可能起源于中肾管的罕见女性附件肿瘤。简要提及了一些重要问题,包括输卵管癌的更新分期、子宫内膜样癌的组织病理学变异及其有时不寻常的模式,这些模式可能与其他肿瘤混淆。最后一部分涵盖了输卵管作为卵巢癌和腹膜癌主要起源部位这一相对较新的概念。讨论了支持输卵管伞端作为浆液性输卵管上皮内癌部位的组织学、免疫组织化学和分子生物学证据,浆液性输卵管上皮内癌可能是高级别卵巢癌和腹膜浆液性癌的直接前体。