Results 21 to 30 of about 2,345 (167)
Cancer, 1978 A rare case of rapidly evolving dysgerminoma produced death by tumor in less than two months after onset of symptoms. It is important to recall that dysgerminoma possesses considerable malignant potential, which infrequently is manifested by rapidly progressive disease.
J J, Gillespie, L K, Arnold
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An aggressive systemic mastocytosis preceded by ovarian dysgerminoma
BMC Cancer, 2020 Background Aggressive systemic mastocytosis (ASM) is a rare malignant disease characterized by disordered mast cell accumulation in various organs. We here describe a female ASM patient with a previous history of ovarian dysgerminoma.
Makiko Tsutsumi +10 more
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Magnetic resonance imaging of pure ovarian dysgerminoma: a series of eight cases
Cancer Imaging, 2021 Background Imaging findings have a prominent role in early and correct identification of ovarian dysgerminoma, the most common ovarian malignant germ cell tumor (OMGCT).
Laura Maria Cacioppa +5 more
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Ovarian Dysgerminoma in Pregnant Women with Viable Fetus: A Rare Case Report
Case Reports in Oncology, 2021 Dysgerminoma is an uncommon malignant tumor arising from the germ cells of the ovary. Its association with pregnancy is extremely rare, with a reported incidence of about 0.2–1 per 100,000 pregnancies.
Reda Youssef +5 more
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Dysgerminoma with Estrogen-Producing Functioning Stroma Presenting Precocious Puberty
Case Reports in Pathology, 2021 Dysgerminoma is a malignant ovarian germ cell tumor, and unlike sex-cord stromal tumors, endocrine manifestation is considered rare. Here, we report the first case of dysgerminoma presenting precocious puberty.
Shunsuke Nagase +8 more
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Dysgerminoma of the ovary [PDF]
Cancer, 1979 From 1938 to 1977, 21 patients with pure dysgerminoma were treated at Memorial and James Ewing Hospitals, now Memorial Sloan-Kettering Cancer Center. Twelve patients were considered to have their initial therapy begun or completed at our institution. Eleven (91.7%) of 12 patients were found free of disease from 2 to 38 years (median 6 years).
J H, Freel +4 more
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Andalas Obstetrics and Gynecology Journal, 2019 Background : Inferior caval syndrom is a rare case. It can caused by compresssion of the tumor mass and paraaortic metastastasis lession of ovarian dysgerminoma.
Madona Utami Dewi, Syamel Muhammad
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Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas. [PDF]
PLoS ONE, 2012 Activating c-KIT mutations (exons 11 and 17) are found in 10-40% of testicular seminomas, the majority being missense point mutations (codon 816). Malignant ovarian dysgerminomas represent ~3% of all ovarian cancers in Western countries, resembling ...
Remko Hersmus +12 more
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Clinical and morphological features of ovarian pure dysgerminoma: a report of a 14 years old girl [PDF]
Archive of Oncology, 2002 Dysgerminoma is best known as the ovarian counterpart of seminoma of the testis Relatively uncommon tumors, dysgerminomas account for less than 2% of all ovarian cancer.
Pop-Trajković Zoran +5 more
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Swyer syndrome (46, XY complete gonadal dysgenesis): A rare case of primary amenorrhea
Philippine Journal of Obstetrics and Gynecology, 2022 Swyer syndrome is a type of gonadal dysgenesis wherein a 46, XY karyotype presents with a female phenotype. It is a rare cause of disorder in sexual development that occurs in 1:100,000 births. Local studies are currently limited to few case reports. Sex-
Pamela Maria P. Mallari +1 more
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