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Juvenile granulosa cell tumor diagnosed in 6-month-old infant with precocious puberty

open access: yesRadiology Case Reports, 2021
Juvenile granulosa cell tumor is a rare tumor diagnosed in children, which can present with precocious puberty. We have reported a case of a 6-month-old female patient who presented with precocious puberty.
Rebecca Hansen, MD   +3 more
doaj   +3 more sources

Granulosa Cell Tumour – A Rare Presentation at Age Twenty [PDF]

open access: yesPakistan Journal of Medicine and Dentistry, 2020
Granulosa cell tumor is a rare type of ovarian tumor, which arises from sex cord stroma. Histologically this tumor has two types and is named according to the common age group they affect; adult granulosa cell tumor (AGCT) and juvenile granulosa cell ...
Munazza Ani   +4 more
doaj   +2 more sources

PMS2 gene mutation results in DNA mismatch repair system failure in a case of adult granulosa cell tumor

open access: yesJournal of Ovarian Research, 2017
Background Granulosa cell tumors are rare ovarian malignancies. Their characteristics include unpredictable indolent growth with malignant potential and late recurrence. Approximately 95% are of adult type. Recent molecular studies have characterized the
Wen-Chung Wang   +2 more
doaj   +2 more sources

Granulosa cell tumor of the ovary: a clinicopathological study of six cases [PDF]

open access: yesJournal of Pathology of Nepal, 2011
Background: Ovarian granulosa cell tumors are rare malignant neoplasms that originate from the sexcord stromal cells of the ovary. The study aims to collate data of all granulosa cell tumors diagnosed in Tribhuvan University Teaching Hospital over the ...
RC Adhikari, A Jha, G Shayami
doaj   +3 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

Delayed menopause due to granulosa cell tumor of the ovary

open access: yesJournal of Mid-Life Health, 2011
A 52-year-old patient presented with complaints of menorrhagia. Endometrial biopsy revealed simple hyperplasia of the endometrium. Total abdominal hysterectomy with bilateral oophorectomy was carried out.
Bhushan Murkey   +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

Adult type granulosa cell tumor of the testis: Radiological evaluation and review of the literature

open access: yesUrology Research and Practice, 2019
A testicular granulosa cell tumor of the adult type is very rare. Isolated case reports and small series have been published in the English literature.
Ioannis Tsitouridis   +5 more
doaj   +2 more sources

Juvenile granulosa cell tumor of the testis: prenatal diagnosis and prescrotal approach [PDF]

open access: yesItalian Journal of Pediatrics, 2012
Neonatal testicular tumors are rare and should be considered in the differential diagnosis of newborn scrotal masses. Juvenile granulosa cell tumor (JGCT) accounts for about 5% of all prepubertal testis tumors.
Bulotta Anna Lavinia   +6 more
doaj   +2 more sources

Extraordinarily Prolonged Disease Recurrence in a Granulosa Cell Tumor Patient

open access: yesCase Reports in Oncology, 2010
Background: Granulosa cell tumors are rare sex cord stromal lesions that comprise approximately 3% of all ovarian neoplasms. The vast majority of granulosa cell tumors are considered indolent but in spite of aggressive management, delayed recurrence is ...
Lisa N. Abaid   +3 more
doaj   +2 more sources

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