Results 11 to 20 of about 1,700,060 (216)

Luteoma of pregnancy masquerading as a granulosa cell tumor [PDF]

open access: yesGynecologic Oncology Reports, 2023
Pregnancy luteomas are rare, nonmalignant lesions thought to be caused by hormonal changes during pregnancy. Granulosa cell tumor is a rare type of ovarian cancer; 10% occur during pregnancy and typically present with elevated inhibin levels.
Naixin Zhang   +9 more
doaj   +2 more sources

The association of enchondromatosis with malignant transformed chondrosarcoma and ovarian juvenile granulosa cell tumor (Ollier disease)

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2017
Objective: Ovarian juvenile granulosa cell tumor has an interesting association with multiple enchondromatosis (Ollier disease and Maffucci syndrome) and should be considered a leading diagnosis when an ovarian mass is found in young patients with these ...
Andrea Burgetova   +8 more
doaj   +2 more sources

Is it time to abandon staging surgery and prolonged follow-up in patients with primary adult-type granulosa cell tumor? [PDF]

open access: yesJournal of Ovarian Research
Background As current literature does not provide sufficient data to support clear guidelines in patients with a rare adult-type granulosa cell tumor, we aim to investigate: (1) whether additional staging surgery following primary surgical treatment is ...
Geertruid J. Brink   +13 more
doaj   +2 more sources

Granulosa cell tumor of ovary: A clinicopathological study of four cases with brief review of literature

open access: yesJournal of Mid-Life Health, 2014
Introduction: Adult granulosa cell tumor (GCT) is a rare ovarian malignancy having good prognosis in comparison with other epithelial tumors. The study aims to collect data of all granulosa cell tumors diagnosed in ESIC Medical College & PGIMSR ...
B R Vani   +3 more
doaj   +2 more sources

Vascular resection and reconstruction in recurrent granulosa cell tumor [PDF]

open access: yesGynecologic Oncology Reports
Introduction: Oncovascular surgery is a rare but important component of radical surgery in gynecologic cancer, requiring interdisciplinary collaboration and coordination.
Lindsey Finch   +5 more
doaj   +2 more sources

Unusual radiologic imaging in juvenile granulosa cell tumor with precocious puberty: A unilocular cyst [PDF]

open access: yesRadiology Case Reports
Juvenile Granulosa Cell Tumor (JGCT) represents 5% of all granulosa cell cancers. Precocious puberty is a frequent feature of this tumor. A 2-year and 2-month-old girl was referred with a diagnosis of suspected ovarian cancer, dysfunctional uterine ...
Nurmilia Afriliani, MD   +1 more
doaj   +2 more sources

Pathogenesis and treatment of adult-type granulosa cell tumor of the ovary

open access: yesAnnals of Medicine, 2017
Markku Heikinheimo   +2 more
exaly   +2 more sources

Adult‐type granulosa cell tumor of the ovary: a FOXL2‐centric disease

open access: yesThe Journal of Pathology: Clinical Research, 2021
Adult‐type granulosa cell tumors (aGCTs) account for 90% of malignant ovarian sex cord‐stromal tumors and 2–5% of all ovarian cancers. These tumors are usually diagnosed at an early stage and are treated with surgery.
Jessica A Pilsworth   +20 more
semanticscholar   +1 more source

Progress in the management of ovarian granulosa cell tumor: A review

open access: yesActa Obstetricia et Gynecologica Scandinavica, 2021
Ovarian granulosa cell tumor (GCT) is a rare, low‐grade malignant tumor that accounts for 70% of the sex cord‐stromal tumors. It has two histopathologic types with different clinical and biologic features: adult GCT and juvenile GCT. Most women diagnosed
Junting Li   +6 more
semanticscholar   +1 more source

Torsion of juvenile granulosa cell ovarian tumor

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Juvenile granulosa cell tumor (JGCT), which is one of the sex cord-stromal tumors of the ovary, is a rare malignancy of childhood. Juvenile type is a rare form that accounts for 5% of granulosa cell tumors. Isosexual precocious puberty is the most common
Şenay Kurtuluş   +2 more
doaj   +1 more source

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