Results 71 to 80 of about 6,228,662 (189)
Adult-type granulosa cell tumor of the testis: report of a case and review of literature
The Pan African Medical Journal, 2017 Granulosa cell tumors is classified into juvenile and adult types and comprise less than 5% of ovarian tumors in women and are much rarer in men which only 45 have been previously reported.
Meriem Elbachir +8 more
doaj +1 more source
Adult‐Onset Juvenile Granulosa Cell Tumor With Early Metastasis: A Rare Case With Fatal Outcome
Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.Background Juvenile granulosa cell tumors (JGCTs) are rare ovarian sex cord–stromal tumors that primarily affect children and adolescents. Their occurrence in adults is exceptionally uncommon and presents unique diagnostic and therapeutic challenges due to limited evidence.
Zainab Chatbi +5 more
wiley +1 more source
Case Reports in Otolaryngology, Volume 2026, Issue 1, 2026.Introduction Nasal chondromesenchymal hamartoma (NCMH) is a rare cause of nasal mass in infants and children. It was first described in 1998, and since then, only 63 previous cases have been reported. Case Report Here, we report a case of a 4‐day‐old neonate with a right‐sided nasal mass presenting with respiratory distress since birth.
Mikiyas Olani +6 more
wiley +1 more source
Prevalence and Management of Nonepithelial Ovarian Cancer in a Sub‐Saharan African Setting
Obstetrics and Gynecology International, Volume 2026, Issue 1, 2026.Background Nonepithelial ovarian cancers (NEOCs) comprise a group of uncommon malignancies which can be challenging to treat. This broad term includes germ cell tumors, sex cord–stromal tumors, and rare types of ovarian cancer, such as small‐cell carcinomas and sarcomas.
Biruck Gashawbeza Batu +5 more
wiley +1 more source
Cancer Reports, Volume 8, Issue 11, November 2025.ABSTRACT Background and Objectives Existing literature on ovarian masses necessitating intervention in children by pediatric surgeons and gynecologists in Low‐ and Middle‐Income Countries is sparse and lacks collaborative standardization in management between the two subspecialties.
Nkhensani C. Mashaba +4 more
wiley +1 more source
Changes in expression of TNF alpha and its receptors mRNAs in oocytes and granulosa cells in mice with experimental immune ovarian failure [PDF]
, 2014 Purpose: To investigate the expression of TNF- α and its receptors (types I and II) at mRNA level in oocytes and granulose cells as well as to study effect of TNF-α on follicular cell death in mice with experimental immune ovarian failure induced by ...
Grushka, Nataliya +4 more
core +1 more source
Virilization and abdominal mass in a newborn female: A case report
Journal of Pediatric Surgery Case Reports, 2017 We describe virilization in a newborn female secondary to bilateral congenital juvenile granulosa cell tumor (JGCT). The patient presented with abdominal mass and ambiguous genitalia at birth, and bilateral ovarian masses were discovered on further ...
Natalie A. Drucker, MD +2 more
doaj +1 more source
Adult Type Granulosa Cell Tumor Causing Precocious Pseudopuberty in a 6 Year-old Girl
, 2003 Malignant ovarian tumors are responsible for 2-3% of all cases of precocious pseudo-puberty (PP) in girls. The most common forms of ovarian tumors presenting as PP are the granulosa cell tumors (GCT).
Adal, E +12 more
core +1 more source
Current views on treatment of the ovarian granulosa-cell tumor [PDF]
, 1970 Summary The granulosa-cell tumor ( folliculoma ) is a rare type of ovarian neoplasm, accounting for 5% of all cases [1]. It is the most common type of sex cord-stromal tumors, diagnosed in 70% of cases.
Kwiatkowski, Mariusz +3 more
core
Enxtraoviarian granulosa cell tumor: a case report [PDF]
, 2016 Extraovarian granulosa cell tumor (GCT) is a very unusually tumor, assumed to arise from the ectopic gonadal tissue along the embryonal route of the genital ridge.
Jai, Saad Rifki +4 more
core +1 more source