Results 1 to 10 of about 189 (107)

Sertoli–Leydig cell tumor of the ovary: A diagnostic dilemma

open access: yesGynecologic Oncology Reports, 2016
Background: Sertoli–Leydig cell tumors are rare sex-cord stromal tumors of the ovary that can present with a variety of histological elements, which may complicate diagnosis and treatment.
Casandra A. Liggins   +2 more
doaj   +3 more sources

Sertoli-Leydig Cell Tumor of Ovary-A Diagnostic Dilemma [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Sertoli Leydig Cell Tumours (SLCTs) are rare, unilateral, sex cord stromal tumours of ovary, which constitute less than 1% of all the ovarian neoplasms. These tumours can be functionally diverse and they may have heterologous elements.
Rohini Dhanya C.S.   +2 more
doaj   +3 more sources

Conservative management of Sertoli‐Leydig cell tumor of the ovary

open access: yesActa Obstetricia et Gynecologica Scandinavica, 1997
Peter Hillemanns   +2 more
doaj   +4 more sources

Bilateral Sertoli-Leydig cell tumor in a primigravida: a rare case

open access: yesRare Tumors, 2014
We present a unique case of incidentally discovered bilateral Sertoli Leydig cell tumor in a primigravida who displayed no features of virilization. The apha fetoprotein levels were elevated.
Ruchita Tyagi   +3 more
doaj   +3 more sources

Sertoli-Leydig cell tumor with DICER1 mutation

open access: yesGynecologic Oncology Reports
Sertoli-Leydig cell tumors (SLCT) are a rare form of sex cord stromal tumors. DICER1 germline mutations have been identified in a portion of these cases. We report a 15-year-old individual who presented to a well-child visit with secondary amenorrhea and
Shae N. Jansen   +2 more
doaj   +3 more sources

Postmenopausal mild hirsutism and hyperandrogenemia due to ovarian Sertoli-Leydig cell tumor: A case report

open access: yesHeliyon, 2020
Among several types of ovarian tumors, Sertoli-Leydig cell tumors are considered significantly rare, accounting for less than 1% of all primary ovarian tumors. Hirsutism caused by ovarian tumors accounts for approximately 1% of all cases of hirsutism. We
Dan Chen   +4 more
doaj   +3 more sources

An Ovarian Sertoli–Leydig Cell Tumor with Elevated Alpha-Fetoprotein in an Adolescent: A Rare Case Report and Literature Review

open access: yesMedicina
An ovarian Sertoli–Leydig cell tumor is a rare type of sex cord–stromal tumor of the ovary. Typically, it presents as abdominal pain or androgenic manifestations in women in the second to third decade of life.
Gabija Žilinskienė   +3 more
doaj   +3 more sources

Retiform Sertoli-Leydig Cell Tumor of the Ovary

open access: yesInternational Journal of Clinical Medicine, 2016
Sertoli-Leydig cell tumor of the ovary is a kind of sex cord-stromal tumor, which occurs between teens and twenties with symptoms including abdominal pain and swelling. The incidence rate is infinitely rare comprising less than 0.5% of all ovarian tumor.
Gyu-Bong Yu   +3 more
exaly   +3 more sources

Ovarian Sertoli-Leydig cell tumor: A case report

open access: yesAsian Journal of Surgery, 2023
Guoyan Liu   +4 more
doaj   +3 more sources

Simultaneous Sertoli Cell-Only Syndrome and Leydig Cell Tumor in a Patient with Azoospermia: A Rare Case Report

open access: yesCase Reports in Oncology, 2022
Testicular cancers comprise 1–1.5% of entire cancers in men, and sex cord-stromal tumors include 5% of testicular cancers. This study aims to report a simultaneous Sertoli cell-only syndrome and Leydig cell tumor in the same patient.
Rawa Bapir   +8 more
doaj   +1 more source

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