Results 11 to 20 of about 233,367 (176)

Case Report: Ovarian dysgerminoma with pseudo-Meigs syndrome in a child [PDF]

open access: yesFrontiers in Pediatrics
Ovarian dysgerminoma is a rare pediatric germ cell tumor, and its association with pseudo-Meigs syndrome (PMS) is exceedingly uncommon. PMS is characterized by massive pleural effusions and ascites accompanying a pelvic mass, which often leads to ...
Zhanhu Li, Dong Chen, Qiang Wei
doaj   +3 more sources

Advanced Ovarian Dysgerminoma With Supraclavicular Lymph Node Metastasis and Peritoneal Carcinomatosis: A Rare Case Report [PDF]

open access: yesClinical Case Reports
Ovarian dysgerminoma is a rare, highly chemo‐sensitive germ cell tumor usually presenting early. We report a FIGO stage IVB case with supraclavicular lymph node metastasis and peritoneal carcinomatosis in a 31‐year‐old woman.
Bishal Khaniya   +5 more
doaj   +3 more sources

OVARIAN DYSGERMINOMA IN PREGNANCY [PDF]

open access: yesAcademic Medical Journal, 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. Approximately 80% of cases are reported in patients younger than 30 years of age (mean age: 21 years), whereas 75% of women with dysgerminomas present with ...
Petrova, Deva   +3 more
openaire   +3 more sources

Clinical and morphological features of ovarian pure dysgerminoma: a report of a 14 years old girl [PDF]

open access: yesArchive 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   +2 more sources

Imaging appearance of ovarian dysgerminoma: A report of two cases

open access: yesRadiology Case Reports
Ovarian dysgerminoma is a rare germ cell tumor accounting for 1%-2% of all malignant ovarian tumors and is generally associated with a good prognosis.
Ghita Lahnine   +8 more
doaj   +2 more sources

Malignant ovarian dysgerminoma in a 16-year-old leopard gecko (Eublepharis macularius) [PDF]

open access: yesVeterinární Medicína, 2023
The 16-year-old female leopard gecko (Eublepharis macularius) was presented with distended coelom and cachexia. Examination of the faecal sample ruled out the presence of protozoan parasites.
H Zborilova   +5 more
doaj   +2 more sources

Ovarian dysgerminoma with Müllerian anomaly: a case report [PDF]

open access: yesObstetrics & Gynecology Science, 2020
Müllerian anomalies are rare deformities in women, and only a few cases concerning gynecologic malignancies arising in patients with congenital uterine malformations have been reported. Herein, we present the case of a 34-year-old woman with dysgerminoma
Ha Na Kim   +8 more
doaj   +2 more sources

Ex vivo oocyte retrieval for fertility preservation in an adolescent patient with recurrent ovarian dysgerminoma: a case report and review of the literature [PDF]

open access: yesF&S Reports
Objective: To describe fertility preservation via ex vivo oocyte retrieval for an adolescent patient undergoing oophorectomy for recurrent ovarian dysgerminoma and to review the available literature regarding this technique.
Addison W. Alley, M.D.   +11 more
doaj   +2 more sources

Ovarian dysgerminoma

open access: yes, 2016
© 2016, University of Kragujevac, Faculty of Science. All Rights Reserved. Ovarian dysgerminoma (OD) is one of the most common malignant tumours of the ovarian germ cells, comprising 1-2% of all malignant ovarian tumours. It most commonly occurs between the ages of 10 and 30.
Devic A.   +3 more
openaire   +3 more sources

Dysgerminoma with Estrogen-Producing Functioning Stroma Presenting Precocious Puberty

open access: yesCase 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
doaj   +2 more sources

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