Simultaneous Sertoli Cell-Only Syndrome and Leydig Cell Tumor in a Patient with Azoospermia: A Rare Case Report [PDF]
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 +2 more sources
Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review [PDF]
Ovarian Leydig cell tumor is a rare type of ovarian steroid cell neoplasms, presenting in only 0.1% of all ovarian tumor cases, and is generally androgen-secreting and unilateral.
Diana Bužinskienė +3 more
doaj +2 more sources
A Boy with 46,XX Karyotype (SRY Double-positive) and a Leydig Cell Tumor [PDF]
Leydig cell tumors are the most common type of testicular sex cord stromal tumors. The presence of the Y chromosome is associated with tumor risk in sex development disorders (DSD), however tumor development without Y chromosome is extremely rare.
Merve Güllü +4 more
doaj +2 more sources
Testicular leydig cell tumor revealed by hydrocele [PDF]
Leydig cell tumor (LCT) is a rare testicular tumor with a low incidence accounting 3% of all testicule neoplasms. Due to its rarity, the natural history of LCT is poorly understood. Patients can present with atypical symptoms and endocrine disorders. The
Wala Ben Kridis +6 more
doaj +2 more sources
Incidental detection of a virilizing Sertoli-Leydig cell tumor during cesarean section: A case report [PDF]
Sertoli-Leydig cell tumors are a rare type of sex cord-stromal tumors that are mostly hormonally active (androgenic or estrogenic). Owing to the rarity of this disease, its impact on pregnancy is not fully understood.
Roza Mahyoob +2 more
doaj +2 more sources
Testis sparing surgery for Leydig cell tumor, surgical approach, and clinical outcome: A case report and review of literature [PDF]
Testicular Leydig cell tumors are rare neoplasms of the testes. These tumors are generally benign but malignancy and metastatic potential have been described.
Faris Abushamma +5 more
doaj +2 more sources
An Ovarian Sertoli–Leydig Cell Tumor with Elevated Alpha-Fetoprotein in an Adolescent: A Rare Case Report and Literature Review [PDF]
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 +2 more sources
Sertoli-Leydig cell tumor with DICER1 mutation [PDF]
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 +2 more sources
Pure Leydig cell tumor of the ovary: a rare presentation of a rare entity in a pregnant patient [PDF]
Aim: Leydig cell tumors (LCT) are rare neoplasms that represent less than 0.1% of all ovarian tumors. This tumor usually presents with signs and symptoms of excess androgen levels. Diagnosis is made based on a combination of history, laboratory findings,
Anwar Rjoop +4 more
doaj +2 more sources
Leydig cell tumors can cause precocious puberty in prepubertal males. Radical orchiectomy is the standard therapy for Leydig cell tumors, with a good overall prognosis.
Jeong Ho Ahn +3 more
doaj +1 more source

