PAX8: A Highly Sensitive Marker for the Glands in Extragenital Endometriosis

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This study evaluated PAX8 as a sensitive epithelial marker for extragenital endometriosis, finding it positive in 95.7% of cases and unaffected by hormonal therapy.

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This study evaluated whether PAX8 is a sensitive epithelial immunohistochemical marker for glands in extragenital endometriosis and compared its staining performance with CD10, ER, and PR. Tissue samples included 8 ovarian endometriomas and 47 extragenital/microscopic endometriosis cases, with the percentage of samples positive for each marker assessed; PAX8 immunostaining was positive in 95.7% (45/47) of extragenital endometrioses and 100% (8/8) of ovarian endometriomas, while CD10 marked stromal cells in 97.9% (46/47). PAX8 showed strong gland staining even in at least one CD10-negative case, and PAX8 and CD10 positivity were not affected by preoperative hormonal therapy, though ER positivity decreased. This paper is centrally about endometriosis — it establishes PAX8 as a highly sensitive epithelial marker for glands in extragenital endometriosis.

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Abstract

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.
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Abstract

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. Similar content being viewed by others

References

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endometriosis

MeSH descriptors

Endometriosis Endometriosis PAX8 Transcription Factor Adult Biomarkers Biomarkers Endometriosis Female Humans Intestinal Mucosa Intestinal Mucosa Intestinal Mucosa Ovary Ovary Ovary PAX8 Transcription Factor Urinary Bladder Urinary Bladder Urinary Bladder

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