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Metastatic juvenile granulosa cell tumor in abdominal wall
Diagnostic Cytopathology, 2023AbstractJuvenile 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, 2022Prior 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, 1990Abstract 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, 2007We 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, 2009Juvenile 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, 2003Juvenile 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, 1988Abstract. 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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Therapy of Advanced Ovarian Juvenile Granulosa Cell Tumors
Klinische Pädiatrie, 2002Gonadal sex cord-stromal tumors are rare tumors that develop from the gonadal non-germ cell component such as granulosa, Sertoli or Leydig cells. Among these, juvenile granulosa cell tumors (JGCT) constitute the largest subgroup of ovarian sex cord-stromal tumors during childhood and adolescence.
D T, Schneider +5 more
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Juvenile granulosa cell tumor.
Clinical imaging, 2003Juvenile granulosa cell tumor (GCT) of the ovary is a rare neoplasm occurring in premenarchal girls and young women. Juvenile GCT that occurs in premenarchal girls usually produces sexual precocity as a consequence of estrogen secretion. Juvenile GCTs are more likely to grow to a relatively large size with a much smaller likelihood of peritoneal spread,
Adam M, Gittleman +5 more
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Gynandroblastoma with Elements Resembling Juvenile Granulosa Cell Tumor
International Journal of Gynecological Pathology, 1997Gynandroblastoma is an extremely rare sex cord-stromal tumor that exhibits significant ovarian and testicular differentiation. In most previously reported tumors, adult granulosa cell tumor has formed the ovarian-type component and Sertoli or Sertoli-Leydig cell tumor (SLCT) has formed the testicular-type component.
J R, Broshears, L M, Roth
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