Results 61 to 70 of about 5,696 (226)
Maedica, 2021 Patients with Swyer syndrome, "XY gonadal dysgenesis", have fibrosed gonads with a significant risk of developing germ cell tumours. During radiological assessment, a 17-year-old female with Swyer syndrome showed mildly enlarged gonads that were removed ...
M. Arafa +5 more
semanticscholar +1 more source
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
openaire +2 more sources
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
doaj +1 more source
Ovarian dysgerminoma in pregnancy
Medicine, 2021 Rationale: Although dysgerminomas are relatively uncommon among all ovarian neoplasms, representing for only about 2%, they account for 32.8 percent of malignant ovarian germ cell tumors. Their association with pregnancy is extremely rare; due to the low
I. Sas +3 more
semanticscholar +1 more source
Dysgerminoma and gonadoblastoma in the course of Swyer syndrome [PDF]
, 2016 We present a case of a woman with primary amenorrhea. Ultrasound imaging showed a uterus of normal size but bands of connective tissues at the site of ovaries. A genetic test was done which revealed the XY karyotype. Swyer syndrome was diagnosed.
Andrzej Wojtyś +19 more
core +1 more source
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
doaj +1 more source
Ovarian dysgerminoma in pregnancy [PDF]
, 2023 Dysgerminoma is a very rare germ cell tumor of the ovary. It constitutes about 1% of all germ cell malignancies and accounts for 1-5% of all ovarian malignancies in the first two decades of life.
Trajkova, Kornelija +3 more
core +1 more source
Pure dysgerminoma of the ovary: CT and MRI features with pathological correlation in 13 tumors
Journal of Ovarian Research, 2020 Background To investigate the spectrum of CT and MRI findings of dysgerminoma of the ovary. Methods CT and MRI imaging of 12 patients with 13 histologically proven dysgerminomas of the ovary were retrospectively reviewed.
Shu-Hui Zhao +7 more
semanticscholar +1 more source
BMC Pregnancy and Childbirth, 2021 Background Ovarian dysgerminoma, a subtype of malignant germ cell tumor (GCT), is a rare ovarian neoplasm that is infrequently found in the gravid patient.
Aneesa Thannickal +4 more
semanticscholar +1 more source
Intracranial Dysgerminomas [PDF]
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 1976 SUMMARY:We have reported three cases of intracranial dysgerminoma. The origin of these tumors has been controversial for a long time. It is now accepted that they develop from germ cells. The diagnosis is often difficult to confirm because of the variety of signs.
G, Leblanc +4 more
openaire +2 more sources