Results 151 to 160 of about 6,228,662 (189)

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.
Stephen D, Frausto, John P, Geisler, Mavis S, Fletcher, Anil K, Sood   +3 more
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Prenatal diagnosis of juvenile granulosa cell tumor of the testis

Journal of Pediatric Urology, 2008
Juvenile granulosa cell tumor is a rare benign neoplasm of the testicular stroma that accounts for 1-5% of all prepubertal testis tumors [Metcalfe PD, Farivar-Mohseni H, Farhat W, McLorie G, Khoury A, Bagli DJ. Pediatric testicular tumors: contemporary incidence and efficacy of testicular preserving surgery.
Chad, Peterson, Steven, Skoog
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Juvenile granulosa cell tumor of the ovary associated with hypercalcemia

Archives of Gynecology and Obstetrics, 2007
Juvenile granulosa cell tumors (JGCTs) are rare ovarian neoplasms that typically occur in children and young women. While most JGCTs are diagnosed in Stage IA and can be cured by unilateral oophorectomy alone, the remainders are diagnosed in more advanced stages and may exhibit aggressive behavior despite surgery and chemotherapy.
Benjamin, Piura, Arnon, Wiznitzer, Ruthy, Shaco-Levy   +2 more
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Juvenile granulosa cell tumor.

Clinical imaging, 2003
Juvenile 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, Anita P, Price, Charles, Coren, Mudnia, Akhtar, Virginia, Donovan, Douglas S, Katz   +5 more
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Unusual presentation of juvenile granulosa cell tumor of the ovary

Journal of Endocrinological Investigation, 2006
We present a case report of juvenile granulosa cell tumor of the ovary (JGCT) with an unusual clinical presentation and hormonal secretion.A 16-yr-old girl had developed spontaneous menarche at the age of 12 yr, but after this initial menstrual bleeding she had no further periods for 4 yr. She had no clinical signs of virilization.
LARIZZA, DANIELA, CALCATERRA, VALERIA, SAMPAOLO, PATRIZIA, G. Lanati, P. Brambilla, T. Mondello, S. Cesari   +6 more
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Management of Advanced Juvenile Granulosa Cell Tumor of the Ovary

Gynecologic Oncology, 1993
Juvenile granulosa cell tumor of the ovary occurs most frequently in young women and children. Ten percent of cases present during pregnancy. The majority of tumors are in FIGO Stage I and have a favorable prognosis. The prognosis of higher stage tumors, however, is generally less favorable.
J L, Powell, N A, Johnson, C L, Bailey, C N, Otis   +3 more
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Juvenile granulosa cell tumor of the ovary

The American Journal of Surgical Pathology, 1984
The clinical and pathological features of 125 juvenile granulosa cell tumors of the ovary were analyzed. The patients ranged in age from newborn to 67 years (average 13 years). Forty-four percent were 10 years of age or younger, 34% between 11 and 20 years, 18% between 21 and 30 years, and 3% over 30 years of age.
R H, Young, G R, Dickersin, R E, Scully
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Therapy of Advanced Ovarian Juvenile Granulosa Cell Tumors

Klinische Pädiatrie, 2002
Gonadal 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, G, Calaminus, R, Wessalowski, R, Pathmanathan, D, Harms, U, Göbel   +5 more
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[Juvenile granulosa-cell tumor: clinical and molecular expression].

Gynecologie, obstetrique & fertilite, 2009
Ovarian sex cord-stromal tumors are rare tumors that originate from the nongerminal cells of ovary. Two decades ago, the identification of juvenile granulosa-cell tumors (GCT), as a specific entity inside this group, allowed a better treatment of these tumors in children.
Kalfa,, N., Philibert, P., Patte, C., Thibaud, E., Pienkowski, C., Ecochard, A., Boizet-Bonhoure, B., Fellous, M., Sultan, C.   +8 more
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Gynandroblastoma with Elements Resembling Juvenile Granulosa Cell Tumor

International Journal of Gynecological Pathology, 1997
Gynandroblastoma 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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