Two Cases of Mesonephric-Like Adenocarcinoma Arising From Ovary and Peritoneal and Literature Review

两例起源于卵巢和腹膜的中肾样腺癌病例报告及文献综述

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Abstract

Reports of Mesonephric-like adenocarcinoma (MLA) arising from other than the ovary and uterus are exceedingly rare. This report details two cases of MLA in patients with a history of endometriosis. One of these two cases is believed to be the first documented case of primary peritoneal MLA. The first case was a 64-year-old woman with a history of hysterectomy and oophorectomy for endometriosis. She presented with International Federation of Gynecology and Obstetrics (FIGO) stage IVB primary peritoneal MLA, diagnosed eight years later via CT-guided biopsy and immunohistochemistry. Despite multiple chemotherapy regimens, she died 13 months after initiation of treatment. The second case was a 72-year-old woman with a history of endometriosis, and she was diagnosed with FIGO stage IIIA1(i) ovarian MLA. She underwent complete cytoreductive surgery followed by adjuvant paclitaxel and carboplatin chemotherapy and remained recurrence-free for three years. A literature review of 66 reported cases of ovarian MLA was conducted to compare clinical characteristics, treatment, and prognosis. According to these findings, 55% were diagnosed at an early stage (FIGO I-II), and prognosis was generally favorable after complete surgical resection, but outcomes were poor for sub-optimally resected cases. These cases suggest a potential link between MLA development and a history of endometriosis, particularly after surgical intervention. The prognosis for MLA is highly dependent on achieving complete surgical resection. Advanced-stage primary peritoneal MLA has a poor prognosis, comparable to conventional primary peritoneal serous carcinoma. Given the difficulty of preoperative diagnosis, diligent follow-up is recommended for high-risk patients with a history of endometriosis. Future research is needed to establish effective treatments for advanced or recurrent disease.

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