Results 11 to 20 of about 15,062 (213)
Testicular granulosa cell tumor, adult type
Indian Journal of Pathology and Microbiology, 2008 Granulosa cell tumor (GCT) of the adult type is a rare and slow-growing neoplasm in the testis. This tumor may be associated with endocrine manifestations and resemble classic GCT of the ovary morphologically. It has a potential for distant metastasis or
Gupta Anshu +3 more
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PMS2 gene mutation results in DNA mismatch repair system failure in a case of adult granulosa cell tumor [PDF]
Journal 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
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AMH producing purely cystic virilizing adult granulosa cell tumor in 17 years old girl: a case report and review of literatures [PDF]
Journal of Ovarian Research, 2023 Background Androgen-producing granulosa cell tumor in adolescent girl is rare condition and clinical characteristics are not fully elucidated. Case presentation Seventeen years old girl complained of secondary amenorrhea was referred to our out-patient ...
Michio Kitajima +8 more
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Adult granulosa cell tumor with minor foci of juvenile granulosa cell tumor in postmenopausal woman: A rare case report. [PDF]
Int J Surg Case Rep, 2021 Granulosa cell tumor (GCT) is a rare neoplasm that is divided into adult GCT (AGCT) and juvenile GCT (JGCT). Generally, a patient will only have the AGCT or JGCT subtypes. Here, we presented the first case of AGTC accompanied by focal JGTC in a postmenopausal woman.A 63-year-old postmenopausal woman came with distended abdomen accompanied by ...
Rustamadji P +3 more
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Adult type granulosa cell tumor in adult testis: report of a case and review of the literature
Rare Tumors, 2011 Granulosa cell tumors can be classified into juvenile and adult types and more commonly occur in ovaries. Adult testicular granulosa cell tumors are extremely rare and only 29 cases of adult type have previously been reported.
Zhanyong Bing +2 more
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Intraoperative scrape cytology: Adult granulosa cell tumor of ovary
Journal of Cytology, 2011 Adult granulosa cell tumor is often a hormonally active stromal cell neoplasm of the ovary with malignant potential. Intra-operative pathological assessment is a valuable tool in guiding optimal surgical treatment in patients.
Prabal Deb, Ajay Malik, Kavita K Sinha
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A case of adult granulosa cell tumor of the testis. [PDF]
Am J Case Rep, 2014 Adult granulosa cell tumors of the testis (AGCTT) are classified as sex cord-stromal tumors. Only 31 cases have been reported. Typical presentation includes a slowly enlarging, painless testicular mass. Associated findings are gynecomastia, decreased libido, and erectile dysfunction.
Tanner SB, Morilla DB, Schaber JD.
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Prognostic factors in adult granulosa cell tumor of the ovary [PDF]
Cancer, 1997 The clinical course of adult granulosa cell tumor of the ovary is characterized by indolent growth tending toward late recurrence. A variety of clinical and pathologic parameters have previously been evaluated for prognostication with inconclusive results.The clinical records and tumor sections of 70 patients with adult granulosa cell tumors of the ...
B E, Miller +5 more
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Adult Granulosa Cell Tumor: A Sinister Differential for Clomiphene-resistant Infertility. [PDF]
J Hum Reprod Sci, 2018 Granulosa cell tumors (GCTs) are rare sex cord-stromal tumors of the ovary. They may present with features of hyperestrogenism. We present a case of a 29-year-old nulliparous female, with infertility and oligomenorrhoea, initially managed with a provisional diagnosis of polycystic ovarian syndrome.
Gainder S, Kaur J, Siwatch S, Gupta N.
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Cytomorphology of adult granulosa cell tumor in ascitic fluid
Indian Journal of Pathology and Microbiology, 2010 Adult granulosa cell tumors (AGCT) are associated with ascites in 10% of the cases. Although these tumors form two per cent of all ovarian tumors, they may create a diagnostic challenge in cytologic preparations.
Azad Kalpana, Khunger Jitender
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