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本文引用的文献

1
BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma.BRCA1、TP53 和 CHEK2 种系突变与子宫浆液性癌相关。
Cancer. 2013 Jan 15;119(2):332-8. doi: 10.1002/cncr.27720. Epub 2012 Jul 18.
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Concurrent endometrial intraepithelial carcinoma (EIC) and serous ovarian cancer: can EIC be seen as the precursor lesion?同时性子宫内膜上皮内癌(EIC)和浆液性卵巢癌:EIC 能否被视为前驱病变?
Int J Gynecol Cancer. 2012 Mar;22(3):457-64. doi: 10.1097/IGC.0b013e3182434a81.
3
TP53 mutations in serous tubal intraepithelial carcinoma and concurrent pelvic high-grade serous carcinoma--evidence supporting the clonal relationship of the two lesions.浆液性输卵管上皮内癌和同期盆腔高级别浆液性癌中的 TP53 突变——支持两种病变克隆关系的证据。
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p53 signature and serous tubal in-situ carcinoma in cases of primary tubal and peritoneal carcinomas and serous borderline tumors of the ovary.p53 特征与原发性输卵管和腹膜癌以及卵巢浆液性交界性肿瘤中输卵管和腹膜内原位癌。
Int J Gynecol Pathol. 2011 Sep;30(5):417-24. doi: 10.1097/PGP.0b013e318216d447.
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Integrated genomic analyses of ovarian carcinoma.卵巢癌的综合基因组分析。
Nature. 2011 Jun 29;474(7353):609-15. doi: 10.1038/nature10166.
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Risk-reducing salpingo-oophorectomy (RRSO) in BRCA mutation carriers: experience with a consecutive series of 111 patients using a standardized surgical-pathological protocol.BRCA 基因突变携带者的预防性输卵管卵巢切除术(RRSO):使用标准化手术病理方案对 111 例连续患者的经验。
Int J Gynecol Cancer. 2011 Jul;21(5):846-51. doi: 10.1097/IGC.0b013e31821bc7e3.
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A proposed model for endometrial serous carcinogenesis.子宫内膜浆液性癌发生的一种假说模型。
Am J Surg Pathol. 2011 Jan;35(1):e1-e14. doi: 10.1097/PAS.0b013e318202772e.
8
"Primary peritoneal" high-grade serous carcinoma is very likely metastatic from serous tubal intraepithelial carcinoma: assessing the new paradigm of ovarian and pelvic serous carcinogenesis and its implications for screening for ovarian cancer.“原发性腹膜”高级别浆液性癌极有可能来源于输卵管上皮内浆液性癌的转移:评估卵巢和盆腔浆液性癌发生的新范例及其对卵巢癌筛查的影响。
Gynecol Oncol. 2011 Mar;120(3):470-3. doi: 10.1016/j.ygyno.2010.11.020. Epub 2010 Dec 14.
9
The impact of tissue block sampling on the detection of p53 signatures in fallopian tubes from women with BRCA 1 or 2 mutations (BRCA+) and controls.组织块取样对 BRCA1 或 2 突变(BRCA+)女性和对照者输卵管中 p53 特征检测的影响。
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10
The molecular pathogenesis of hereditary ovarian carcinoma: alterations in the tubal epithelium of women with BRCA1 and BRCA2 mutations.遗传性卵巢癌的分子发病机制:BRCA1 和 BRCA2 突变妇女的输卵管上皮改变。
Cancer. 2010 Nov 15;116(22):5261-71. doi: 10.1002/cncr.25439.

早期子宫浆液性癌子宫内膜和输卵管上皮前驱病变的特征分析

Characterization of precursor lesions in the endometrium and fallopian tube epithelium of early-stage uterine serous carcinoma.

作者信息

Tolcher Mary C, Swisher Elizabeth M, Medeiros Fabiola, Lima Joema F, Hilderbrand Jodi L, Donovan Janis L, Garcia Rochelle L, Cliby William A, Dowdy Sean C

机构信息

Department of Obstetrics and Gynecology (M.C.T., W.A.C., S.C.D.), Division of Gynecologic Surgery Department of Laboratory Medicine and Pathology (F.M., J.F.L., J.L.H., J.L.D.), Mayo Clinic, Rochester, Minnesota Departments of Obstetrics and Gynecology (E.M.S.) Pathology (R.L.G.), Division of Gynecologic Oncology, University of Washington, Seattle, Washington.

出版信息

Int J Gynecol Pathol. 2015 Jan;34(1):57-64. doi: 10.1097/PGP.0000000000000109.

DOI:10.1097/PGP.0000000000000109
PMID:25473754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4405903/
Abstract

To determine if selected cases of uterine serous carcinoma (USC) arise from tubal rather than endometrial epithelium. Bilateral fallopian tubes from 38 women with pure USC were entirely submitted for histopathologic examination using the protocol Sectioning and Extensively Examining the FIMbria (SEE-FIM). Non-neoplastic endometrium was extensively sampled. Immunohistochemistry for p53 was performed on all paraffin blocks of fallopian tube and non-neoplastic endometrium. Endometrial intraepithelial carcinoma (EIC) was present in 22 cases (58%). Endometrial p53 foci were identified in 3 patients. There were 11 cases (29%) with fallopian tube involvement; 9 of 11 had tubal wall invasion or lymphatic involvement without serous tubal intraepithelial carcinoma (STIC) and were, therefore, classified as metastatic from the endometrium. STIC was identified in 3 patients (8%). There were 3 cases with tubal p53 foci in non-neoplastic epithelium. EIC was present in 58% of patients, further supporting EIC as a precursor lesion to USC. STIC was present in 8%, suggesting that the fallopian tube may in fact represent the primary lesion in a minority of patients with USC. This finding may account for the early multifocal disease distribution observed in these patients.

摘要

为确定所选子宫浆液性癌(USC)病例是起源于输卵管上皮而非子宫内膜上皮。对38例纯USC患者的双侧输卵管全部按照输卵管伞端切片及广泛检查(SEE-FIM)方案进行组织病理学检查。对非肿瘤性子宫内膜进行广泛取材。对所有输卵管和非肿瘤性子宫内膜石蜡块进行p53免疫组化检测。22例(58%)存在子宫内膜上皮内癌(EIC)。3例患者发现子宫内膜p53病灶。11例(29%)有输卵管受累;11例中的9例有输卵管壁浸润或淋巴受累但无浆液性输卵管上皮内癌(STIC),因此被归类为子宫内膜转移。3例患者(8%)发现STIC。3例非肿瘤性上皮中有输卵管p53病灶。58%的患者存在EIC,进一步支持EIC作为USC的前驱病变。8%的患者存在STIC,提示输卵管实际上可能是少数USC患者的原发部位。这一发现可能解释了这些患者中观察到的早期多灶性疾病分布情况。