TY - JOUR
T1 - Mesonephric-like adenocarcinoma of the endometrium: detailed molecular characterization of the first case showing a morphological continuum from mesonephric-like metaplasia and atypical mesonephric-like hyperplasia to adenocarcinoma
AU - Santoro, Angela
AU - Angelico, Giuseppe
AU - Narducci, Nadine
AU - Travaglino, Antonio
AU - Piermattei, Alessia
AU - Inzani, Frediano
AU - Arciuolo, Damiano
AU - Addante, Francesca
AU - Urtueta, Belen Padial
AU - Tinnirello, Giordana
AU - Scaglione, Giulia
AU - D'Alessandris, Nicoletta
AU - Valente, Michele
AU - Minucci, Angelo
AU - Zannoni, Gian Franco
PY - 2025
Y1 - 2025
N2 - Mesonephric-like adenocarcinoma is a rare subtype of endometrial cancer, characterized by its histological and molecular overlap with mesonephric carcinoma of the uterine cervix. This study presents a unique case of mesonephric-like adenocarcinoma in the endometrium, accompanied by adjacent mesonephric-like hyperplasia and atypical mesonephric-like hyperplasia. Histologically, the transition from mesonephric metaplasia to adenocarcinoma was evident, and molecular analysis revealed shared mutations, including KRAS (p.G12D) in both atypical hyperplasia and adenocarcinoma, and a novel BCOR mutation (p.A1314Nfs*49) in the adenocarcinoma. These findings suggest a Müllerian origin of mesonephric-like adenocarcinoma via mesonephric transdifferentiation, challenging the traditional understanding of mesonephric histogenesis. The identification of these mutations underscores the potential for targeted therapies, particularly in cases with BCOR and KRAS mutations. This study is the first to document preneoplastic lesions in mesonephric-like adenocarcinoma, offering new insights into its pathogenesis and therapeutic implications.
AB - Mesonephric-like adenocarcinoma is a rare subtype of endometrial cancer, characterized by its histological and molecular overlap with mesonephric carcinoma of the uterine cervix. This study presents a unique case of mesonephric-like adenocarcinoma in the endometrium, accompanied by adjacent mesonephric-like hyperplasia and atypical mesonephric-like hyperplasia. Histologically, the transition from mesonephric metaplasia to adenocarcinoma was evident, and molecular analysis revealed shared mutations, including KRAS (p.G12D) in both atypical hyperplasia and adenocarcinoma, and a novel BCOR mutation (p.A1314Nfs*49) in the adenocarcinoma. These findings suggest a Müllerian origin of mesonephric-like adenocarcinoma via mesonephric transdifferentiation, challenging the traditional understanding of mesonephric histogenesis. The identification of these mutations underscores the potential for targeted therapies, particularly in cases with BCOR and KRAS mutations. This study is the first to document preneoplastic lesions in mesonephric-like adenocarcinoma, offering new insights into its pathogenesis and therapeutic implications.
KW - BCOR
KW - Endometrial cancer
KW - Mesonephric hyperplasia
KW - Mesonephric carcinoma
KW - KRAS
KW - BCOR
KW - Endometrial cancer
KW - Mesonephric hyperplasia
KW - Mesonephric carcinoma
KW - KRAS
UR - http://hdl.handle.net/10807/311979
U2 - 10.1007/s00428-024-03972-9
DO - 10.1007/s00428-024-03972-9
M3 - Article
SN - 1432-2307
SP - 1
EP - 8
JO - Virchows Archiv
JF - Virchows Archiv
ER -