Results 51 to 60 of about 1,885 (186)
Tumor de células da granulosa e gravidez.
Acta Médica Portuguesa, 2003 Ovary tumor and pregnancy is a rare and serious condition with an unexpected outcome as it can interfere with the course of pregnancy. The authors report a case of a large juvenile granulosa cell tumor diagnosed at 33 weeks of pregnancy during a routine ...
Ana Paula Machado +4 more
doaj +1 more source
Central precocious puberty and granulosa cell ovarian tumor in an 8-year old female
Pediatric Reports, 2013 Ovarian tumors associated with hormonal changes of the peripheral iso-sexual precocious puberty are of common presentation. We describe here a rare case of juvenile granulosa cell tumor in a female with central precocious puberty (CPP).
Valeria Calcaterra +9 more
doaj +1 more source
Personalized Models of Biological Barriers and Their Diseases: Recent Progress with Organs‐On‐Chips
Advanced Biology, Volume 10, Issue 2, February 2026.Buck and Bugter et al. explore the architectural diversity and physiological functions of human barrier systems and reveal how organ‐on‐chip platforms, particularly those integrating patient‐derived cells, are advancing barrier disease modeling. They highlight how emerging biological and technological advances can be used to bridge the gap between ...
Franziska Buck +4 more
wiley +1 more source
The molecular mechanism of ovarian granulosa cell tumors
Journal of Ovarian Research, 2018 Over these years, more and more sex cord-stromal tumors have been reported. Granulosa cell tumor (GCT) is a rare tumor in ovaries, accounts for 2% to 5% of ovarian cancers.
Jiaheng Li +3 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
, 2023 ObjectiveThe aim of this study was to explore the symptoms, treatment, and pathogenesis of ovarian juvenile granulosa cell tumors with Ollier’s disease in children.MethodsFrom October 2019 to October 2020, clinical data were retrospectively analyzed for ...
Renwu Hua (12415246) +7 more
core +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
Galactorrhea-associated granulosa cell tumor in a child
, 2004 Granulosa cell tumor of the ovary is a rare form of ovarian cancer in children. An 11-year-old girl was admitted with complaints of galactorrhea and abdominal mass. Abdomino-pelvic ultrasound and computed tomography revealed an ovarian tumor.
Koksal, Y +5 more
core +1 more source
Juvenile Granulosa Cell Tumor with an Unusual Clinical Course: A Late-onset and Late Recurrent Case [PDF]
, 2020 Juvenile granulosa cell tumors (JGCTs) are rare ovarian tumors with overall good prognoses. They differ from adult granulosa cell tumors (AGCTs), which are well known for late recurrence.
Fushimi, Soichiro +8 more
core +1 more source