Kindelberger David W, Lee Yonghee, Miron Alexander, Hirsch Michelle S, Feltmate Colleen, Medeiros Fabiola, Callahan Michael J, Garner Elizabeth O, Gordon Robert W, Birch Chandler, Berkowitz Ross S, Muto Michael G, Crum Christopher P
Division of Women's and Perinatal Pathology, Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA.
Am J Surg Pathol. 2007 Feb;31(2):161-9. doi: 10.1097/01.pas.0000213335.40358.47.
Proposed origins of pelvic serous carcinoma include the ovary, fallopian tube, and peritoneum. Prophylactic salpingo-oophorectomies in BRCA+ women have recently identified the fimbria as a site of origin for early serous carcinoma (tubal intraepithelial carcinoma or TIC). We explored the relationship of TIC to pelvic serous carcinomas in consecutive cases with complete adnexal exam (SEE-FIM protocol). Cases positive (group A) or negative (group B) for endosalpinx (including fimbria) involvement, were subclassified as tubal, ovarian, or primary peritoneal in origin. Coexisting TIC was recorded in group A when present and p53 mutation status was determined in 5 cases. Of 55 evaluable cases, 41 (75%) were in group A; including tubal (n = 5), peritoneal (n = 6), and ovarian (n = 30) carcinomas. Foci of TIC were identified in 5 of 5, 4 of 6, and 20 of 30, respectively. Ninety-three percent of TICs involved the fimbriae. Five of 5 TICs and concurrent ovarian carcinomas contained identical p53 mutations. Thirteen of 14 cases in group B were classified as primary ovarian carcinomas, 10 with features supporting an origin in the ovary. Overall, 71% and 48% of "ovarian" serous carcinomas had endosalpinx involvement or TIC. TIC coexists with all forms of pelvic serous carcinoma and is a plausible origin for many of these tumors. Further studies are needed to elucidate the etiologic significance of TIC in pelvic serous carcinoma, reevaluate the criteria for tubal, peritoneal, and ovarian serous carcinoma, and define the role of the distal tube in pelvic serous carcinogenesis.
盆腔浆液性癌的可能起源部位包括卵巢、输卵管和腹膜。BRCA基因阳性女性的预防性输卵管卵巢切除术最近发现,输卵管伞端是早期浆液性癌(输卵管上皮内癌或TIC)的起源部位。我们采用完整附件检查方案(SEE-FIM方案),对连续病例中TIC与盆腔浆液性癌的关系进行了研究。根据输卵管内膜(包括伞端)受累情况,将病例分为阳性组(A组)或阴性组(B组),并根据起源部位进一步分为输卵管型、卵巢型或原发性腹膜型。A组病例若存在共存的TIC则予以记录,并对5例病例测定p53突变状态。在55例可评估病例中,41例(75%)属于A组;包括输卵管癌(n = 5)、腹膜癌(n = 6)和卵巢癌(n = 30)。在5例输卵管癌、6例腹膜癌和30例卵巢癌中,分别有5例、4例和20例发现了TIC病灶。93%的TIC累及输卵管伞端。5例TIC及同时存在的卵巢癌中有5例含有相同的p53突变。B组14例病例中有13例被归类为原发性卵巢癌,其中10例具有支持卵巢起源的特征。总体而言,71%的“卵巢”浆液性癌存在输卵管内膜受累或TIC。TIC与所有类型的盆腔浆液性癌共存,并且可能是许多此类肿瘤的起源。需要进一步研究以阐明TIC在盆腔浆液性癌中的病因学意义,重新评估输卵管、腹膜和卵巢浆液性癌的诊断标准,并明确远端输卵管在盆腔浆液性癌发生中的作用。