Abstract:Mesonephric adenocarcinoma (MNA) is believed to arise from benign mesonephric remnants or hyperplasia located in the lateral walls of the uterine cervix. They are uncommon in other sites of the gynecologic tract, and exceptionally rare in the uterine corpus. So far, only 30 cases of uterine MNA have been reported in the literature, as a result, the etiology, clinical behavior, choice of treatment, and histogenesis of uterine MNA are still unclear. In this study, we report 2 cases of MNA of uterine corpus. One … Show more
“…The diagnosis of either true mesonephric adenocarcinoma or MLA is challenging on biopsy materials and frozen sections as it shares many similar features to clear cell carcinoma, serous carcinoma, endometrial carcinoma and carcinosarcoma. However, true mesonephric adenocarcinoma and MLA will display limited pseudo-stratification a single layer off cuboidal lining and the presence of eosinophilic secretion in the lumen ( Zhang, 2019 ). To reiterate, the terminology of ‘mesonephric-like’ adenocarcinoma is being used when describing tumors of primary ovarian or endometrial origin, as the etiology of these tumors outside of the cervix is only recently described and the histogenesis is not proven.…”
Highlights
Mesonephric-like adenocarcinomas (MLA) of the ovary are rare, require differentiation from other histiotypes.
True histiogenesis of MLA of ovary remains debated, possibly arise from mullerian lesions of the ovary.
MLA of ovary have differing genotypes from true mesonephric carcinomas of the cervix.
Case described reflects further evidence for mullerian origin of MLA of ovary, with endometriosis in affected ovary.
MLA of ovary can act aggressively, case described recurred and responded only partially to chemotherapy.
“…The diagnosis of either true mesonephric adenocarcinoma or MLA is challenging on biopsy materials and frozen sections as it shares many similar features to clear cell carcinoma, serous carcinoma, endometrial carcinoma and carcinosarcoma. However, true mesonephric adenocarcinoma and MLA will display limited pseudo-stratification a single layer off cuboidal lining and the presence of eosinophilic secretion in the lumen ( Zhang, 2019 ). To reiterate, the terminology of ‘mesonephric-like’ adenocarcinoma is being used when describing tumors of primary ovarian or endometrial origin, as the etiology of these tumors outside of the cervix is only recently described and the histogenesis is not proven.…”
Highlights
Mesonephric-like adenocarcinomas (MLA) of the ovary are rare, require differentiation from other histiotypes.
True histiogenesis of MLA of ovary remains debated, possibly arise from mullerian lesions of the ovary.
MLA of ovary have differing genotypes from true mesonephric carcinomas of the cervix.
Case described reflects further evidence for mullerian origin of MLA of ovary, with endometriosis in affected ovary.
MLA of ovary can act aggressively, case described recurred and responded only partially to chemotherapy.
“…Mesonephric-like adenocarcinomas (M-LAC) are rare, recently described tumors occurring in the uterine corpus and ovary, which share the same morphological and immunohistochemical features with more common mesonephric adenocarcinoma (MAC), most commonly arising in the uterine cervix [ 1 – 5 ]. Despite the similarities between these tumors, the histogenesis of M-LAC is still disputable, as this type of tumor occurs outside the anatomical areas in which mesonephric remnants/hyperplasia may normally occur.…”
Background: Mesonephric-like adenocarcinoma (M-LAC) is a rare, recently described tumor occurring in the uterine corpus and ovary, which shares the same morphological and immunohistochemical features with the more common mesonephric adenocarcinoma (MAC), which mostly arises the uterine cervix. Despite the similarities between these tumors, the histogenesis of M-LAC is still disputable. Case presentation: Sixty-one-year-old woman presented with an advanced tumor of the left ovary with intraabdominal spread and liver metastases. After receiving 5 cycles of neoadjuvant chemotherapy, she underwent a hysterectomy with bilateral salpingo-oophorectomy, and resection of the liver metastasis, omentum, and appendix. Histologically, the ovarian tumor consisted of two components, whose morphology and immunohistochemical results were typical of either a serous borderline tumor (immunohistochemical positivity for PAX8, WT1, ER and PR) or a mesonephric-like carcinoma (immunohistochemical positivity for PAX8, TTF1 and GATA3). Only the component of the mesonephric-like adenocarcinoma metastasized to the omentum and liver. A molecular analysis with a panel of 271 genes (size 1020 kbp) was performed separately on samples from the borderline tumor, primary ovarian mesonephric-like adenocarcinoma, and liver metastasis. The results showed the clonal origin of all samples, which shared the same KRAS (NM_004985.3:c.34G > T, p.(G12C)) and PIK3CA (NM_ 006218.2:c.1633G > A, p.(E545K)) somatic mutations. Moreover, in the sample from the primary mesonephric-like carcinoma and its liver metastasis a likely pathogenic somatic MYCN mutation (NM_005378.4:c.131C > T, p.(P44L) was found. In all samples, the deletion of exons 9-10 in the CHEK2 gene was present, which is in concordance with the previously performed genetic testing of the blood specimen which revealed the hereditary CHEK2 mutation in this patient.
“…10,13 Benign proliferative mesonephric lesions include a scope of symptomatic lesions associated to a diffuse hyperplastic process that may have a deeply infiltrative appearance, like hyperplasia of mesonephric remnants. 7,13 They are unusual conditions that are the common origin of mesonephric carcinomas, and demand a differential diagnosis from it. 7,13 The cytological and architectural features are the base for the mesonephric adenocarcinoma diagnosis.…”
Section: Discussionmentioning
confidence: 99%
“…7,13 They are unusual conditions that are the common origin of mesonephric carcinomas, and demand a differential diagnosis from it. 7,13 The cytological and architectural features are the base for the mesonephric adenocarcinoma diagnosis. For this reason, it is fundamental that the clinical approach allows for obtaining tumor biopsies.…”
Introduction Malignant mesonephric tumors are uncommon in the female genital tract, and they are usually located where embryonic remnants of Wolffian ducts are detected, such as the uterine cervix. The information about these tumors, their treatment protocol, and prognosis are scarce.
Case report A 60-year-old woman with postmenopausal vaginal bleeding was initially diagnosed with endometrial carcinoma. After suspicion co-testing, the patient underwent a loop electrosurgical excision of the cervix and was eventually diagnosed with mesonephric adenocarcinoma. She was subjected to a radical hysterectomy, which revealed International Federation of Gynecology and Obstetrics (FIGO) IB1 stage, and adjuvant radiotherapy. The follow-up showed no evidence of recurrence after 60 months.
Conclusion We present the case of a woman with cervical mesonephric adenocarcinoma. When compared with the literature, this case had the longest clinical follow-up without evidence of recurrence, which reinforces the concept that these tumors are associated with a favorable prognosis if managed according to the guidelines defined for the treatment of patients with cervical adenocarcinomas. Though a rare entity, it should be kept in mind as a differential diagnosis for other cervical cancers.
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