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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]

Clinical 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, Noushin Afshar Moghaddam, Masoomeh Raoufi, Maryam Iranipour, Samar Moghadami   +4 more
doaj   +3 more sources

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

Gynecologic 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, Shuqi Zuo, Min Cui, Xingbo Zhao, Xiaoyi Qi   +4 more
doaj   +2 more sources

Hypercalcemia associated with dysgerminoma and elevation of calcitriol: A case report and review of the literature

SAGE Open Medical Case Reports, 2022
We report on the case of a patient with dysgerminoma, a rare germ cell tumor, which showed hypercalcemia with an elevation of 1α,25-dihydroxycholecalciferol (calcitriol). A 27-year-old nulliparous woman presented with hypercalcemia during the examination
Fumiyoshi Yakou, Hirotsugu Suwanai, Hironori Abe   +2 more
exaly   +2 more sources

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

Medicina (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, Ludmila Lozneanu, Elena Cojocaru   +2 more
exaly   +3 more sources

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

Diagnostic 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]

Clinical 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, José Loba, Ramata Kouakou‐Kouraogo, Carine Houphouet‐Mwandji, Roland Adjoby   +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]

Veterinary 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, Farhang Sasani, Saeed Farzad‐Mohajeri, Mohsen Tovhidifar, Iradj Ashrafi Tamai   +4 more
doaj   +2 more sources

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

Frontiers 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, Min You, Xiaoyun Zhang, Jingjing Wei, Guangyao Lin, Qianjue Tang, Lianwei Xu   +6 more
doaj   +2 more sources

Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the Literature [PDF]

JCRPE
Gonadoblastoma is a rare gonadal tumor composed of sex cord cells and primitive germ cells. While the majority of gonadoblastomas are found in individuals with 46,XY gonadal dysgenesis, they are also rarely seen in patients with a 46,XX karyotype.
Tugce Kandemir, Esin Karakilic Ozturan, Ozlem Dural, Ayca Dilruba Aslanger, Elif Inan Balci, Aysel Bayram, Semen Onder, Asli Derya Kardelen, Melek Yildiz, Sukran Poyrazoglu, Firdevs Bas, Feyza Darendeliler   +11 more
doaj   +2 more sources

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

Archive 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