Ovarian female adnexal tumor of probable Wolffian origin – Case report
نویسندگان
چکیده
منابع مشابه
Female adnexal tumor of probable Wolffian origin.
Female adnexal tumor of probable Wolffian origin (FATWO) is a rare neoplasm arising from the remnants of the mesonephric duct. We report here a case of FATWO in a 70-year-old woman arising from the broad ligament and confirmed on immunohistochemistry. Most of these tumors behave in a benign fashion but certain histological features like hypercellularity, cellular pleomorphism and nuclear atypia...
متن کاملA case of metastatic female adnexal tumor of probable Wolffian origin
•We present a case of female adnexal tumor of probable Wolffian origin progressed rapidly while it is classified in LPM.•This case suggests that recurrence can occur within 1 year in patients with tumor implants at initial surgery.
متن کاملA female adnexal tumor of probable Wolffian origin showing positive O-6-methylguanine-DNA methyltransferase methylation
Female adnexal tumor of probable Wolffian origin (FATWO) is a rare disease entity that arises from the mesonephric duct system. FATWO is different than other gynecological cancers in terms of embryology. Here, we describe the case of a 52-year-old woman with malignant FATWO. The patient underwent explorative laparotomy and surgical staging after a frozen section revealed malignancy. Detailed ex...
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In view of the small number of recurrent and metastatic cases of female adnexal tumors of probable Wolffian origin (FATWO), there is a distinct lack of evidence to support recommendations regarding treatment. In the present study, a 37-year-old female was diagnosed with a left adnexal tumor and underwent a left salpingo-oophorectomy (SO). The tumor was found to arise from the left tubal fimbria...
متن کاملClinicopathological characteristics of ovarian low-grade malignant Wolffian adnexal tumor: a case report
Wolffian adnexal tumor (WAT) is a rare tumor with low potential of malignancy. Most cases appear to behave in a benign fashion, but recurrence and metastasis has also been reported. Malignant ovarian WAT is exceptionally rare. Here we report one case of WAT, in order to explore its clinicopathological/immunohistochemical characteristics, and differential diagnosis. The patient is a 63-year old ...
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ژورنال
عنوان ژورنال: Open Medicine
سال: 2021
ISSN: 2391-5463
DOI: 10.1515/med-2021-0306