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Ovarian Seromucinous Borderline Tumor and Clear Cell Carcinoma: An Unusual Combination

机译:卵巢血清核交界性肿瘤和透明细胞癌:异常的组合。

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摘要

Ovarian seromucinous borderline tumors (SMBTs) are rare. They architecturally resemble serous borderline tumors but are much more frequently associated with endometriosis. The coexistence of other tumors with seromucinous tumors is also extremely rare. Here, we report an unusual combination of bilateral ovarian SMBT and clear cell carcinoma associated with polypoid endometriosis of the colon, in a 62-year-old woman. There was no transitional lesion between the two tumors. Immunohistochemistry showed different staining patterns in tumor components. Seromucinous tumor cells were positive for estrogen receptor (ER) and progesterone receptor (PgR) but negative for Napsin A, p504S, and HNF1B. Clear cell tumor cells were positive for Napsin A and p504S and focally positive for HNF1B but negative for ER and PgR. Loss of ARID1A expression was not observed in SMBTs, clear cell tumors, or endometriosis. These findings suggest that these tumors arose from separate endometriosis foci and collided within the same ovary. To the best of our knowledge, this is the first case of this unusual combination of ovarian seromucinous tumor and clear cell carcinoma to be reported in the English literature.
机译:卵巢血清粘液性交界性肿瘤(SMBT)很少见。它们在结构上类似于浆液性交界性肿瘤,但更常与子宫内膜异位症相关。其他肿瘤与浆液性肿瘤并存的情况也极为罕见。在这里,我们报道了一名62岁女性的双侧卵巢SMBT和透明细胞癌的异常组合,与结肠息肉样子宫内膜异位症相关。两种肿瘤之间没有过渡病变。免疫组织化学在肿瘤成分中显示出不同的染色模式。浆液性肿瘤细胞的雌激素受体(ER)和孕激素受体(PgR)阳性,但对Napsin A,p504S和HNF1B阴性。透明细胞肿瘤细胞对Napsin A和p504S呈阳性,对HNF1B呈局部阳性,但对ER和PgR呈阴性。在SMBT,透明细胞肿瘤或子宫内膜异位症中未观察到ARID1A表达缺失。这些发现表明,这些肿瘤起源于单独的子宫内膜异位灶,并在同一卵巢内发生碰撞。据我们所知,这是英国文献报道的卵巢浆液性肿瘤与透明细胞癌这种异常组合的首例病例。

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