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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
exaly   +4 more sources

Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas. [PDF]

open access: yesPLoS 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   +9 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

Ovarian Dysgerminoma Associated With Pregnancy Presenting as Hemoperitoneum: An Obstetric Case Report [PDF]

open access: yesClinical Case Reports
Ovarian dysgerminomas are malignant tumors that are infrequently associated with pregnancy. These tumors are typically detected in cases of abdominal pain or during routine imaging such as ultrasound or magnetic resonance imaging.
Eléonore Gbary‐Lagaud   +4 more
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

Spontaneous pregnancy after fertility‐sparing surgery and adjuvant chemotherapy for advanced pure dysgerminoma: A case report [PDF]

open access: yesClinical Case Reports
Key Clinical Message Fertility‐sparing surgery and appropriate adjuvant chemotherapy for advanced malignant ovarian germ cell tumors have excellent survival results and promising reproductive and obstetric outcomes.
Göksu Göç   +4 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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