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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
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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.
D, Fink, R A, Kubik-Huch, S, Wildermuth
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Metastatic juvenile granulosa cell tumor in abdominal wall

Diagnostic Cytopathology, 2023
AbstractJuvenile granulosa cell tumor (JGCT) is an uncommon ovarian tumor. There are only a few cases in the literature that depict the cytomorphology of JGCT at the primary/metastatic site. We described the fine‐needle aspiration cytology of a recurrent metastatic JGCT of the anterior abdominal wall, 5 years post‐surgery (total abdominal hysterectomy ...
Dipanwita Biswas   +3 more
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Juvenile granulosa cell tumor associated with Ollier disease

Skeletal Radiology, 2022
Prior case reports have described synchronous ovarian juvenile granulosa cell tumor (JGCT) and enchondromatosis in patients with Ollier disease and Maffucci syndrome. We present a case of a juvenile granulosa cell tumor with an IDH1 somatic mutation identified in the ovarian tissue in a 15-year-old female who presented with abnormal vaginal bleeding ...
Laurel A, Littrell   +3 more
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Ovarian juvenile granulosa cell tumors

Adolescent and Pediatric Gynecology, 1990
Abstract Ovarian neoplasms, though rarely seen in children or adolescents, are very important biologically due to their potential to affect growth, development, and fertility in these patients; therefore, prompt diagnosis is imperative. Ovarian juvenile granulosa cell tumors (JGCT) occur predominantly in the first two decades of life.
Charles V. Biscotti   +1 more
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Juvenile Granulosa Cell Tumor of the Epididymis

Urologia Internationalis, 2007
We report the first case of a juvenile granulosa cell tumor of the epididymis in a young man. Clinical and histological findings are presented and the clinical significance of the case is discussed.
Stavros, Gravas   +3 more
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Ovarian Juvenile Granulosa Cell Tumors in Infants

Journal of Pediatric Hematology/Oncology, 2009
Juvenile ovarian granulosa cell tumors (JGCTs) are described infrequently in pediatrics, and their finding in prepubertal patients is exceptional. Most of the tumors are benign, but recurrences up to 4 years of follow-up have been described. We present 2 cases of JGCT in infants: 1 with late recurrence of bilateral ovarian JGCT and 1 in a newborn with ...
Moisés, Leyva-Carmona   +2 more
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Juvenile granulosa cell tumor of the testis

Urology, 2003
Juvenile granulosa cell tumor of the testis is a rare type of intermediate stromal cell tumor. Only 11 cases of juvenile granulosa cell tumor of the testis have been reported to the national tumor registry as of December 2001. We report an additional case of primary juvenile granulosa cell tumor of the testis. The benign lesion was managed successfully
Randy, Fagin   +4 more
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Cystic Juvenile Granulosa Cell Tumor of the Ovary

Acta Obstetricia et Gynecologica Scandinavica, 1988
Abstract. Sex cord‐stromal tumors comprise approximately 5% of ovarian neoplasms and among these the granulosa cell tumor is the one most commonly seen (1).Two histopathologically well defined patterns of granulosa cell tumor are known: the common adult granulosa cell tumor (AGCT), and the less frequent juvenile granulosa cell tumor (JGCT) (1,2,3,4 ...
E, Spaun, K, Glavind
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