Rabban Joseph T, Crawford Beth, Chen Lee-May, Powell Catherine B, Zaloudek Charles J
Department of Pathology, Cancer Risk Program, Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, CA 94143, USA.
Am J Surg Pathol. 2009 Jan;33(1):111-9. doi: 10.1097/PAS.0b013e31817d74a7.
Germline mutations in the hereditary breast/ovary carcinoma genes BRCA1 or BRCA2 confer increased lifetime risk for ovarian, fallopian tube, and primary peritoneal carcinoma. This risk can be minimized by prophylactic surgery. Risk-reducing salpingo-oophorectomy (RRSO) provides 2 potential benefits: long-term cancer risk reduction and immediate detection of occult early carcinoma, which frequently arises in the tubal fimbriae. Recognition of occult early tubal carcinoma is challenging because it is often microscopic in size and can be confined to the fimbrial epithelium without invasion. Transitional cell metaplasia is a benign epithelial alteration that is a common finding in the serosa of the tube but is underrecognized in the tubal fimbriae, where it may mimic tubal intraepithelial carcinoma. The aim of this study was to define the incidence, morphology, immunophenotype, and distribution of transitional cell metaplasia of the fimbriae in RRSO specimens from 96 women with BRCA germline mutations and to compare these features to those of tubal intraepithelial carcinoma in this cohort. RRSO specimens from an additional 30 women at increased risk for ovarian cancer based on strong family history were also studied, along with RRSO from 1 patient with Lynch syndrome, and 1 patient with PTEN mutation. Transitional cell metaplasia of the fimbriae was present in 26% of all RRSO specimens. It was commonly multifocal (67%), with involvement of the tip, edges, or base of the fimbrial plicae. Average size of a metaplastic focus was 1.3 mm (range: 0.1 to 10 mm). None of the metaplastic foci expressed p53 by immunohistochemistry nor was there increased staining for the proliferation marker MIB-1. Occult early carcinoma was detected in 6/128 RRSO specimens. Median tumor size was 2.7 mm (range: 1 to 11 mm). All expressed p53 and showed markedly increased MIB-1 staining. The key criteria distinguishing transitional cell metaplasia from tubal intraepithelial carcinoma were uniform cell size and shape, normal nucleus:cytoplasm ratios, lack of nuclear atypia, presence of nuclear grooves, lack of mitoses, and absence of p53 expression or increased staining for MIB-1. No particular clinical variables (BRCA 1 vs. BRCA 2 mutation, parity, personal history of breast cancer, prior abdomino-pelvic surgery, or intraoperative findings) or benign pathologic alterations in the RRSO specimens were associated with the presence of transitional cell metaplasia of the fimbriae. None of the patients with this finding developed peritoneal carcinoma during follow-up ranging from 1 month to 9 years. This study demonstrates that transitional cell metaplasia of the fimbriae is a common benign finding in RRSO specimens that should not be confused with the much less common finding of tubal intraepithelial carcinoma.
遗传性乳腺癌/卵巢癌基因BRCA1或BRCA2的种系突变会增加患卵巢癌、输卵管癌和原发性腹膜癌的终生风险。这种风险可通过预防性手术降至最低。降低风险的输卵管卵巢切除术(RRSO)有两个潜在益处:长期降低癌症风险以及即时检测隐匿性早期癌,这种癌常发生于输卵管伞端。隐匿性早期输卵管癌的识别具有挑战性,因为其通常体积微小,可能局限于伞端上皮而无浸润。移行细胞化生是一种良性上皮改变,常见于输卵管浆膜,但在输卵管伞端较少被认识到,在那里它可能酷似输卵管上皮内癌。本研究的目的是确定96例携带BRCA种系突变女性的RRSO标本中输卵管伞端移行细胞化生的发生率、形态、免疫表型及分布,并将这些特征与该队列中输卵管上皮内癌的特征进行比较。还研究了另外30例基于家族病史患卵巢癌风险增加的女性的RRSO标本,以及1例林奇综合征患者和1例PTEN突变患者的RRSO标本。输卵管伞端移行细胞化生存在于所有RRSO标本的26%中。它通常为多灶性(67%),累及伞褶的尖端、边缘或基部。化生灶的平均大小为1.3毫米(范围:0.1至10毫米)。通过免疫组织化学,化生灶均未表达p53,增殖标志物MIB-1的染色也未增加。在128例RRSO标本中检测到6例隐匿性早期癌。肿瘤中位数大小为2.7毫米(范围:1至11毫米)。所有病例均表达p53,且MIB-1染色明显增加。区分移行细胞化生与输卵管上皮内癌的关键标准为细胞大小和形状均匀、核质比正常、无核异型性、存在核沟、无核分裂以及无p53表达或MIB-1染色增加。RRSO标本中没有特定的临床变量(BRCA1与BRCA2突变、生育情况、乳腺癌个人史、既往腹盆腔手术或术中发现)或良性病理改变与输卵管伞端移行细胞化生的存在相关。在1个月至9年的随访期间,有此发现的患者均未发生腹膜癌。本研究表明,输卵管伞端移行细胞化生是RRSO标本中常见的良性表现,不应与罕见得多的输卵管上皮内癌相混淆。