Arakawa Tomoko, Fukuda Shinya, Hirata Tetsuya, Neriishi Kazuaki, Wang Yu, Takeuchi Arisa, Saeki Ai, Harada Miyuki, Hirota Yasushi, Matsumoto Takashi, Koga Kaori, Wada-Hiraike Osamu, Kurihara Masatoshi, Fujii Tomoyuki, Osuga Yutaka
1 Department of Obstetrics and Gynecology, University of Tokyo, Tokyo, Japan.
2 Department of Gynecology, Osaka Central Hospital, Tokyo, Japan.
Reprod Sci. 2019 Feb 14:1933719119828095. doi: 10.1177/1933719119828095.
In cases of extragenital endometriosis or microscopic endometriosis lesions, pathological diagnosis can be challenging because endometriotic stroma and glands represent only a minor component of fibrotic endometriotic lesions. For better accuracy of diagnosis, the development of a sensitive and specific epithelial marker is beneficial. Previous studies showed that PAX8 is a highly sensitive and specific marker for primary and metastatic Mullerian epithelial tumors. Therefore, we sought to examine whether PAX8 is a highly sensitive marker for glands in extragenital endometriosis. Eight and 47 samples of ovarian endometrioma and extragenital endometriosis, respectively, were evaluated in this study. We calculated the percentage of samples positively immunostained for PAX8, CD10, estrogen receptor (ER), and progesterone receptor (PR). PAX8 was positive for endometriotic epithelial cells in 95.7% (45/47) of extragenital endometrioses and in 100% (8/8) of ovarian endometrioses. CD10 was positive for endometriotic stromal cells in 97.9% (46/47) of extragenital endometrioses. PAX8 was strongly positive for glands, even in a CD10-negative case. The expression of PAX8, CD10, and PR was not affected by preoperative hormonal therapy, and the positive rate of ER staining was significantly reduced by preoperative hormonal therapy. In conclusion, PAX8 is a highly sensitive epithelial marker for extragenital endometriosis. This specific expression was maintained under hormonal therapy. It is noteworthy that extragenital endometriosis maintains the expression of this lineage marker, although it occurs at various sites, and its cause and mechanism of development might be different. PAX8 nuclear expression can be useful in detecting extragenital endometriosis in clinical practice.
在生殖器外子宫内膜异位症或微小子宫内膜异位症病变的情况下,病理诊断可能具有挑战性,因为子宫内膜异位间质和腺体仅占纤维化子宫内膜异位病变的一小部分。为了提高诊断的准确性,开发一种敏感且特异的上皮标志物是有益的。先前的研究表明,PAX8是原发性和转移性苗勒管上皮肿瘤的高度敏感和特异的标志物。因此,我们试图研究PAX8是否是生殖器外子宫内膜异位症腺体的高度敏感标志物。本研究分别评估了8例卵巢子宫内膜异位囊肿和47例生殖器外子宫内膜异位症的样本。我们计算了PAX8、CD10、雌激素受体(ER)和孕激素受体(PR)免疫染色阳性的样本百分比。PAX8在95.7%(45/47)的生殖器外子宫内膜异位症和100%(8/8)的卵巢子宫内膜异位症的异位内膜上皮细胞中呈阳性。CD10在97.9%(46/47)的生殖器外子宫内膜异位症的异位间质细胞中呈阳性。即使在CD10阴性的病例中,PAX8在腺体中也呈强阳性。PAX8、CD10和PR的表达不受术前激素治疗的影响,而术前激素治疗可使ER染色阳性率显著降低。总之,PAX8是生殖器外子宫内膜异位症的一种高度敏感的上皮标志物。这种特异性表达在激素治疗下得以维持。值得注意的是,生殖器外子宫内膜异位症尽管发生在不同部位,但其发生原因和发展机制可能不同,但仍维持这种谱系标志物的表达。PAX8核表达在临床实践中有助于检测生殖器外子宫内膜异位症。