Results 1 to 10 of about 15,062 (213)

Adult granulosa cell tumor with rare pulmonary presentation [PDF]

open access: yesRespiratory Medicine Case Reports
Adult granulosa cell tumor (GCT) is an uncommon sex cord-stromal neoplasm of the ovary. It typically demonstrates locoregional spread, and disease outside of the pelvis as metastasis is uncommon.
Mark G. Evans   +5 more
doaj   +4 more sources

Adult granulosa cell tumor of the testis masquerading as hydrocele [PDF]

open access: yesInternational Brazilian Journal of Urology, 2015
Adult testicular granulosa cell tumor is a rare, potentially malignant sex cord-stromal tumor, of which 30 cases have been described to date. We report the case of a 43-year-old male who complained of a left testicular swelling. Scrotal ultrasound showed
Archana George Vallonthaiel   +4 more
doaj   +6 more sources

Adult‐type granulosa cell tumor: An unusual testicular tumor [PDF]

open access: yesClinical Case Reports, 2021
Adult type granulosa cell tumours are extremely rare. Albeit mostly benign, 10% have malignant potential associated with unfavorable pathological features.
Alain Mwamba Mukendi   +3 more
doaj   +3 more sources

Primary extraovarian adult granulosa cell tumor of the greater omentum: a case report and literature review [PDF]

open access: yesFrontiers in Oncology
Extraovarian adult granulosa cell tumors are rare. The diagnosis of extraovarian adult granulosa cell tumors is challenging. Here we presented a case of extraovarian adult granulosa cell tumor originating in the greater omentum.
Ying Zeng, Liang Lv, Liping Luo
doaj   +2 more sources

Collision Tumor of the Ovary: Adult Granulosa Cell Tumor and Mesonephric-like Adenocarcinoma [PDF]

open access: yesDiagnostics
Collision tumors of the ovaries are rare, with only a few reports in the literature. Adult granulosa cell tumors are a relatively common primary tumor component of previously reported collision tumors.
Yujin Lee   +5 more
doaj   +2 more sources

Adult granulosa cell tumor associated with endometrial carcinoma: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2011
Introduction If strict criteria for the diagnosis of carcinoma are used and all patients with granulosa cell tumors are considered, the best estimate of the incidence of associated endometrial carcinomas is under 5%.
Eke Ahizechukwu C   +3 more
doaj   +2 more sources

Benign ovarian thecoma with markedly elevated serum inhibin B levels mimicking adult granulosa cell tumor [PDF]

open access: yesGynecologic Oncology Reports, 2020
Introduction: Elevated serum inhibin B is a classic marker of adult granulosa cell tumors. Here we discuss an extremely rare and informative case of elevated inhibin B associated with an ovarian thecoma.
Erica V. Carballo   +5 more
doaj   +2 more sources

Synchronous occurrence of adult granulosa cell tumor with fibroma in one ovary and brenner tumor in other ovary: An extremely unusual case [PDF]

open access: yesJournal of Mid-Life Health, 2023
Ovarian tumors are a common form of neoplasia in women and it accounts for about 30% of female genital cancers. A coexistence of ovarian tumors with the same histogenetic origin such as germ cell or epithelial or sex cord stromal, but different ...
Alka Yadav   +5 more
doaj   +2 more sources

Granulosa cell tumor of the ovary and antecedent of adjuvant tamoxifen use for breast cancer [PDF]

open access: yesWorld Journal of Surgical Oncology, 2010
Background Adult granulosa cell tumor associated with antecedent use of tamoxifen as adjuvant hormonotherapy for breast cancer is rare. The pathogenesis of this occurrence remains difficult to explain.
Abahssain Halima   +4 more
doaj   +3 more sources

Meigs’ syndrome and adult-type granulosa cell tumor

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2021
Objective: Adult-type granulosa cell tumors (GCT) are sex cord-stromal tumors and often accompanied with abdominal distention and hyperestrogenism-related symptoms. Adult-type GCT-presenting ascites and pleural effusion is extremely rare.
Szu-Ting Yang   +5 more
doaj   +3 more sources

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