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Am J Surg Pathol ; 46(1): 124-133, 2022 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-34183523

RESUMO

Mesonephric-like adenocarcinomas (MLA) are rare neoplasms arising in the uterine corpus and ovary which have been added to the recent 2020 World Health Organization Classification of Female Genital Tumors. They have similar morphology and immunophenotype and exhibit molecular aberrations similar to cervical mesonephric adenocarcinomas. It is debated as to whether they are of mesonephric or Mullerian origin. We describe the clinical, pathologic, immunohistochemical, and molecular features of 5 cases of extrauterine mesonephric-like proliferations (4 ovary, 1 extraovarian), all with novel and hitherto unreported features. These include an origin of MLA in extraovarian endometriosis, an association of ovarian MLA with high-grade serous carcinoma, mixed germ cell tumor and mature teratoma, and a borderline ovarian endometrioid tumor exhibiting mesonephric differentiation. Four of the cases exhibited a KRAS variant and 3 also a PIK3CA variant. In reporting these cases, we expand on the published tumor types associated with MLA and report for the first time a borderline tumor exhibiting mesonephric differentiation. We show the value of molecular testing in helping to confirm a mesonephric-like lesion and in determining the relationship between the different neoplastic components. We provide further evidence for a Mullerian origin, rather than a true mesonephric origin, in some of these cases. We also speculate that in the 2 cases associated with germ cell neoplasms, the MLA arose out of the germ cell tumor.


Assuntos
Adenocarcinoma/patologia , Ductos Paramesonéfricos/patologia , Neoplasias Ovarianas/patologia , Neoplasias Peritoneais/patologia , Ductos Mesonéfricos/patologia , Adenocarcinoma/química , Adenocarcinoma/genética , Adenocarcinoma/terapia , Adulto , Idoso , Idoso de 80 Anos ou mais , Biomarcadores Tumorais/análise , Biomarcadores Tumorais/genética , Diferenciação Celular , Proliferação de Células , Classe I de Fosfatidilinositol 3-Quinases/genética , Feminino , Humanos , Mesocolo/química , Mesocolo/patologia , Pessoa de Meia-Idade , Ductos Paramesonéfricos/química , Mutação , Neoplasias Ovarianas/química , Neoplasias Ovarianas/genética , Neoplasias Ovarianas/terapia , Neoplasias Peritoneais/química , Neoplasias Peritoneais/genética , Neoplasias Peritoneais/terapia , Proteínas Proto-Oncogênicas p21(ras)/genética , Resultado do Tratamento , Ductos Mesonéfricos/química
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