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Stage IIIC Bilateral Dysgerminoma in a 16‐Year‐Old Phenotypic Female With 46,XY Complete Gonadal Dysgenesis and Primary Amenorrhea: A Case Report [PDF]

open access: yesClinical Case Reports
Dysgerminoma, the most common malignant ovarian germ cell tumor, has a significantly increased incidence in individuals with 46,XY complete gonadal dysgenesis (Swyer syndrome). However, primary amenorrhea is the hallmark presentation of Swyer syndrome in
Mahshid Vasef   +4 more
doaj   +3 more sources

Uncommon Metastasis of Ovarian Dysgerminoma: A Case Report and Review of the Literature

open access: yesMedicina (Lithuania), 2021
Ovarian malignant germ cell tumors (OMGCT) represent less than 10% of all ovarian tumors. Dysgerminoma is the most common malignant primitive germ cell tumor in young women, known for its curability and low propensity to invade and metastasize when ...
Elena Cojocaru   +2 more
exaly   +4 more sources

A case report: false hCG trail: dysgerminoma imitates gestational trophoblastic disease [PDF]

open access: yesAJOG Global Reports
Ovarian malignant germ cell tumors (MOGCTs) represent approximately 5% of all ovarian malignancies. However, in women aged 10 to 30, they account for up to 70% of ovarian neoplasms and may occasionally occur bilaterally.
Anna Babkova, PhD   +7 more
doaj   +2 more sources

First-trimester ovarian dysgerminoma in pregnancy: a case report highlighting the value of expert ultrasound [PDF]

open access: yesFrontiers in Oncology
BackgroundMalignant germ cell tumors are rare ovarian malignancies, accounting for less than 5% of ovarian cancers. Dysgerminoma is the most common subtype but remains exceptionally rare during pregnancy, with an estimated incidence of 0.2–1 per 100,000 ...
Natālija Vedmedovska   +8 more
doaj   +2 more sources

Ovotesticular disorders of sex development with dysgerminoma in a 46, XX/46, XY female: A case report [PDF]

open access: yesGynecologic Oncology Reports
The diagnosis of ovotesticular disorders of sex development can only be confirmed when both testicular and ovarian tissues are present simultaneously in the same individual, regardless of the patient’s karyotype. This report aims to discuss the diagnosis
Yafei Xue   +4 more
doaj   +2 more sources

Cytological diagnosis of dysgerminoma associated with pregnancy via peritoneal effusion analysis: a case report [PDF]

open access: yesDiagnostic Pathology
Background Dysgerminoma, a uncommon malignant neoplasm originating from primitive ovarian germ cells, is exceptionally rare during pregnancy. While several studies have documented dysgerminoma diagnosis via peritoneal effusion cytology, no cases ...
Liyan Huang, Lian Xu
doaj   +2 more sources

Co‐Occurrence of Ovarian Dysgerminoma‐Inducing Gonadoblastoma and Two Distinct Mammary Carcinomas in a Dog: A Case Report and Review of the Literature [PDF]

open access: yesVeterinary Medicine and Science
Gonadoblastoma (GB) is an extremely rare mixed gonadal neoplasm, encountered in animals as well as humans. The tumour is typically reported in dysgenetic gonads of those suffering from disorders of sex development and bearing the Y chromosome.
Diba Golchin   +4 more
doaj   +2 more sources

Diagnosis and management of a rare bilateral ovarian mixed germ cell tumor: a case report [PDF]

open access: yesFrontiers in Oncology
BackgroundMixed ovarian malignant germ cell tumors (MOGCTs) are rare neoplasms composed of two or more malignant germ cell components, representing less than 1% of all ovarian germ cell tumors.
Xuanling Li   +6 more
doaj   +2 more sources

Unique combination of an ovarian dysgerminoma, streak ovary and uterine agenesis in a girl of 12 [PDF]

open access: yesArchive of Oncology, 2008
Dysgerminoma of the ovary is a rare malignancy. It is common in dysegenetic ovaries. The prognosis is excellent if treated properly. This is a case report of a girl with agenesis of the uterus, streak ovary and dysgerminoma. Her external genitalia seemed
Dangal Ganesh
doaj   +1 more source

Imaging Findings in Dysgerminoma in a Case of 46 XY, Complete Gonadal Dysgenesis (Swyer syndrome) [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
A 46 XY pure gonadal dysgenesis also known as Swyer syndrome. These patients are phenotypic females with normal female external genitalia and absent testicular tissue.
Pratiksha Yadav   +2 more
doaj   +1 more source

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