Female Adnexal Tumor of Probable Wolffian Origin in the Setting of Peutz-Jeghers Syndrome
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Obstetrics and Gynecology,Pathology and Forensic Medicine
Reference4 articles.
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3. Increased risk for cancer in patients with the Peutz-Jeghers syndrome;Boardman;Ann Intern Med,1998
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1. STK11 Adnexal Tumor: Exploring the Association With Peutz-Jeghers Syndrome and its Distinction From Morphologic Mimickers;Advances in Anatomic Pathology;2024-09-03
2. Ovarian Mucinous Tumor Presenting Atypical Lobular Endocervical Glandular Hyperplasia-Like Appearance in a Patient With Germline STK11 p.F354L Variant: A Case Report;International Journal of Surgical Pathology;2023-05-24
3. The complex and often confusing history, histology and histogenesis of mesonephric, STK11 adnexal tumour and mesonephric‐like neoplasms of the upper female genital tract (including broad ligament);Histopathology;2022-05-18
4. Everolimus plus anastrozole for female adnexal tumor of probable Wolffian origin (FATWO) with STK11 mutation;Gynecologic Oncology Reports;2021-08
5. A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor);American Journal of Surgical Pathology;2021-01-29
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