PMID- 37566876 OWN - NLM STAT- MEDLINE DCOM- 20240422 LR - 20240425 IS - 1538-7151 (Electronic) IS - 0277-1691 (Print) IS - 0277-1691 (Linking) VI - 43 IP - 3 DP - 2024 May 1 TI - Comprehensive Immunohistochemical Analysis of Mesonephric Marker Expression in Low-grade Endometrial Endometrioid Carcinoma. PG - 221-232 LID - 10.1097/PGP.0000000000000976 [doi] AB - Immunohistochemical markers shown to be useful in identifying/confirming mesonephric/mesonephric-like differentiation (MLD markers) include thyroid transcription factor (TTF1), GATA-binding protein 3 (GATA3), and cluster of differentiation 10 (CD10). Only a few studies have examined the expression levels of MLD markers in endometrial endometrioid carcinomas (EECs). This study aimed to analyze the frequency and pattern of MLD marker expression in low-grade EECs. We performed immunostaining for the detection of TTF1, GATA3, and CD10 expression in 50 low-grade EEC tissue samples and evaluated their staining proportion and intensity. Nine tumors (18.0%) expressed at least one MLD marker in varying proportions and intensities, and 2 of these tumors were positive for 2 MLD markers (TTF1/GATA3 and GATA3/CD10, respectively). Three (6.0%) tumors showed moderate-to-strong nuclear TTF1 immunoreactivity in /=15%. Three tumors (6.0%) were focal (mean proportion, 15%) but strongly positive for CD10. Our findings indicate that a subset of EEC can express one or more MLD markers with varying staining proportions and intensities. Given that a diagnosis of uterine mesonephric-like adenocarcinoma should be established based on a combination of characteristic histologic features, unique immunophenotypes, and confirmed molecular findings, pathologists should not exclude EEC based only on the presence of focal immunoreactivity for MLD markers. Awareness of the atypical expression patterns of MLD markers in EEC helps pathologists avoid misdiagnosing EEC as a uterine mesonephric-like adenocarcinoma. CI - Copyright (c) 2023 The Author(s). Published by Wolters Kluwer Health, Inc. FAU - Lee, Yurimi AU - Lee Y AD - Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea (Y.L., S.C., H.-S.K.). FAU - Choi, Sangjoon AU - Choi S FAU - Kim, Hyun-Soo AU - Kim HS LA - eng PT - Journal Article DEP - 20230811 PL - United States TA - Int J Gynecol Pathol JT - International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists JID - 8214845 RN - 0 (Biomarkers, Tumor) SB - IM MH - Female MH - Humans MH - *Carcinoma, Endometrioid/pathology MH - Mesonephros/pathology MH - Uterus/pathology MH - *Adenocarcinoma/pathology MH - Biomarkers, Tumor/metabolism MH - *Endometrial Neoplasms/metabolism PMC - PMC11022992 COIS- The authors declare no conflict of interest. EDAT- 2023/08/11 18:42 MHDA- 2024/04/22 06:43 PMCR- 2024/04/17 CRDT- 2023/08/11 16:52 PHST- 2024/04/22 06:43 [medline] PHST- 2023/08/11 18:42 [pubmed] PHST- 2023/08/11 16:52 [entrez] PHST- 2024/04/17 00:00 [pmc-release] AID - 00004347-990000000-00100 [pii] AID - IJGP22-5228 [pii] AID - 10.1097/PGP.0000000000000976 [doi] PST - ppublish SO - Int J Gynecol Pathol. 2024 May 1;43(3):221-232. doi: 10.1097/PGP.0000000000000976. Epub 2023 Aug 11.