Results 171 to 180 of about 29,048 (222)
Erratum to "Juvenile granulosa cell tumor diagnosed in 6-month-old infant with precocious puberty" [Radiology Case Reports 16 (2021) 2609-2613]. [PDF]
Hansen R, Lewis A, Sullivan C, Hirsig L.
europepmc +1 more source
A testicular mass found to be a rare testicular adult-type granulosa cell tumor: A case report and literature review. [PDF]
Rezzoug F +5 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Journal of the American Veterinary Medical Association, 1975
SUMMARY Unilateral ovariectomy was performed on 3 mares affected with granulosa cell tumors. Tumor fluid in each mare was found to contain estrogen, testosterone, and progesterone. In 2 mares, preoperative blood plasma concentrations of these hormones were comparable to those of a series of clinically normal mares.
R L, Stickle +3 more
openaire +3 more sources
SUMMARY Unilateral ovariectomy was performed on 3 mares affected with granulosa cell tumors. Tumor fluid in each mare was found to contain estrogen, testosterone, and progesterone. In 2 mares, preoperative blood plasma concentrations of these hormones were comparable to those of a series of clinically normal mares.
R L, Stickle +3 more
openaire +3 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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 +2 more sources
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 +2 more sources
Extraovarian Granulosa Cell Tumor
Gynecologic Oncology, 1999The aim of this study was to report a case of extraovarian granulosa cell tumor and to describe its relevance to the histologic origin of granulosa cell tumors and to clinical practice.The clinical course and histopathology of the case were reviewed, and a literature search for other reported cases was performed.A 67-year-old woman presented with ...
J B, Robinson +4 more
openaire +2 more sources
OVARIAN GRANULOSA CELL TUMOR AND ACROMEGALY
The Journal of Clinical Endocrinology & Metabolism, 1949AMENORRHEA is one of the most consistent and usually one of the earliest symptoms of pituitary tumor in women. Menstrual function may return, however, even after a prolonged period of amenorrhea, following surgical removal of the tumor, its shrinkage by roentgen irradiation, or possibly in rare instances following the escape of the expanding tumor from
openaire +2 more sources
Bilateral granulosa cell tumors
American Journal of Obstetrics and Gynecology, 1941Abstract Bilateral tumors of the ovaries were discovered when the child was fourteen weeks of age, and the tumors were successfully removed when she was sixteen weeks of age. Two years and eight months later these tumors were determined to be granulosa cell tumors. The patient seems to be the youngest yet to be reported to have had this disease. When
Erhart E. Zemke, Wallace E. Herrell
openaire +1 more source

