Results 131 to 140 of about 1,885 (186)

Primary extraovarian adult granulosa cell tumor of the greater omentum: a case report and literature review. [PDF]

Front Oncol
Zeng Y, Lv L, Luo L.
europepmc   +1 more source

Liver metastasis of ovarian granulosa cell tumors: a case report and literature review. [PDF]

BMC Womens Health
Zhao L, Jiao T, Zheng L, Yan J, Ma X, Li A, Zhang X, Zhang Y.   +7 more
europepmc   +1 more source

Management of ovarian granulosa cell tumor in childhood: a case report and recommendations for a multidisciplinary approach. [PDF]

Front Oncol
Arnaboldi SMC, Gattuso G, Nicolosi ML, Molinari S, Bettini LR, Leva E, Passoni P, Chiappa V, Daolio C, Balduzzi AC, Massimino M, Terenziani M, Cattoni A.   +12 more
europepmc   +1 more source

Improving diagnosis and management of pediatric ovarian masses: development of a risk stratification model incorporating sonographic and clinical features. [PDF]

BMC Pediatr
Chu L, Chen Z, Zhang M, Cai T, Zhang M, Lu S.   +5 more
europepmc   +1 more source

Mechanistic understanding of female reproductive aging based on the chicken model. [PDF]

J Anim Sci Biotechnol
Zhang J, Gao M, Sun C, Yang N.
europepmc   +1 more source

Pediatric and young adult ovarian masses: clinical approach, diagnostic evaluation, and management. [PDF]

Front Pediatr
Bayramoglu Z, Timur B, Kızmazoglu D, Timur HT, Ulusoy O, Aktas S, Olgun N, Kurt S.   +7 more
europepmc   +1 more source

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Juvenile granulosa cell tumor

Abdominal Imaging, 2001
We present three-dimensional computed tomographic findings of a juvenile granulosa cell tumor of the ovary at FIGO stage IA in a 17-year-old woman. Juvenile granulosa cell tumor is one of the rare sex cord stromal tumors of the ovary. Most tumors at FIGO stage IA have a favorable prognosis, whereas those at higher stages have a less favorable outcome.
Rahel A Kubik-Huch, Simon Wildermuth, Fink D   +2 more
exaly   +4 more sources

Juvenile Granulosa Cell Tumor of the Ovary: A Clinicopathologic Study

Journal of Pediatric and Adolescent Gynecology, 2017
To report on the clinical characteristics and outcome of pediatric patients with juvenile granulosa cell tumor (JGCT) of the ovary. DESIGN, SETTING, PARTICIPANTS, INTERVENTIONS, AND MAIN OUTCOME MEASURES: Patients with histopathologically confirmed ovarian JGCT diagnosed between 1990 and 2016 were identified. Data on the clinical presentation, surgical
Stephanie A Pangas, Karen W Eldin, Kalyani R Patel   +2 more
exaly   +3 more sources

Late recurrence of juvenile granulosa cell tumor of the ovary

American Journal of Obstetrics and Gynecology, 2004
Juvenile granulosa cell tumor (JGCT) of the ovary, if diagnosed at an early stage, has a favorable prognosis. Recurrences are uncommon but typically occur within the first year. The patient presented here was treated with a left oophorectomy after initial presentation.
Mavis S Fletcher, Anil K Sood
exaly   +3 more sources

Juvenile Granulosa Cell Tumor

Pediatric Pathology, 1990
A 2-year-old girl presented with isosexual precocity, and a juvenile granulosa cell tumor of the left ovary was removed. The tumor was unusual in that striated muscle differentiation of the tumor cells was demonstrated. This suggests that the mesenchymal cells retain the potential for divergent differentiation.
F, Raafat, H, Klys, G, Rylance
openaire   +4 more sources