Results 71 to 80 of about 233,367 (176)

Mixed Gonadal Dysgenesis: A Comprehensive Review of Clinical Spectrum, Diagnostic Strategies, and Management Approaches

Clinical Endocrinology, Volume 104, Issue 2, Page 92-102, February 2026.
ABSTRACT Background Mixed gonadal dysgenesis (MGD) is a rare form of differences in sex development (DSD) typically associated with 45,X/46,XY mosaicism. The phenotypic presentation of MGD varies from atypical genitalia to typical male or female appearances often associated with Turner stigmata.
Dinesh Giri, Sushil Yewale, Hannah Hickingbotham, Cara Williams, Mohamed Shalaby, Julie Alderson, Julie Park   +6 more
wiley   +1 more source

Feasibility and Safety of Intraoperative Oocyte Retrieval in Patients With Ovarian Tumor: Results From the Japan Oncofertility Registry

Reproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Purpose To evaluate the clinical utility and safety of intraoperative oocyte retrieval (IOR) as a fertility preservation (FP) strategy for patients with ovarian tumors using data from the Japan Oncofertility Registry (JOFR). Methods This retrospective study analyzed data from 226 patients with ovarian tumors registered in the JOFR between ...
Futa Ito, Satoshi Kubota, Taro Yagi, Mizuho Akedo, Yuta Tsuji, Masahiko Takemura, Ken‐ichirou Morishige   +6 more
wiley   +1 more source

Recurrent ovarian dysgerminoma in pregnancy: a rare case of successful maternal and fetal outcome [PDF]

Dysgerminoma is a rare malignant ovarian germ cell tumor that typically affects women younger than age 30 and is highly sensitive to chemotherapy. Its occurrence during pregnancy is uncommon and recurrence during an ongoing pregnancy is extremely rare ...
Thakare, Sarika S., Tinwani, Sneha B.
core   +1 more source

Advanced‐Stage Gonadal Dysgerminoma in a Patient With a Previous Diagnosis of Familial Swyer Syndrome: A Very Rare Genetic Entity

Case Reports in Medicine, Volume 2026, Issue 1, 2026.
Introduction Swyer syndrome is a genetic abnormality characterized by a 46,XY karyotype in a phenotypically female individual. Affected individuals typically have average or tall stature, unambiguous genitalia at birth, the presence of Müllerian structures, and bilateral streak gonads.
Süleyman Cemil Oğlak, Nilgün Söğütçü, Sedat Akgöl, Özgür Adıgüzel, Hümeyra Elif Ateş Eminoğlu, Gizem Güzel, Veysi Balcı, Emine Acar, Abdullah Acar, Fuat Bozan, Aneek Das Bhowmik   +10 more
wiley   +1 more source

Two cases report of a malignant germ cell tumour of ovary and a granulosa cell tumour:Interest of tumoral immunochemistry in the identification and management.

Frontiers in Oncology, 2014
Objective: In this article, we present two case reports. The first case was a malignant germ cell tumor of the right ovary in a 23 year old female and a case of a bilateral undifferentiated granulosa cell tumor in a 71 year old female.
Jean eBouquet De Jolinière
doaj   +1 more source

Dysgerminoma of the ovary with precocious puberty: a case report.

, 2007
Ovarian dysgerminoma is usually hormonally inert, but when it contains syncytiotrophoblastic giant cells or undergoes malignant transformation, the level of estradiol might be elevated.
Lee, JP, Kim, HY, Chang, KH, Ryu, HS, Mun, SH, Song, ES, Han, JH   +6 more
core   +1 more source

Ovarian dysgerminoma in a pre-pubertal girl: A case report

Journal of Pediatric Surgery Case Reports
Introduction: Ovarian dysgerminoma is a rare malignant germ cell tumor that rarely occurs in pre-puberal girls. Case presentation: An eight-year-old girl presented with a year-long history of progressive, painless abdominal distension and significant ...
Evance Salvatory Rwomurushaka, Patrick Amsi, Jay Lodhia   +2 more
doaj   +1 more source

Ovarian dysgerminoma. A clinico-pathologic study.

, 1984
The authors present the clinical, pathologic and therapeutic report on 5 cases of ovarian dysgerminoma in patients between 15 and 30 years of age, classified as Stage Iai in 3 cases and Stage III in 2 cases.
RESTA, Leonardo, Sabatini R, Restaino A.
core  

Postmenopausal dysgerminoma: unveiling a rare ovarian tumour a case report and review of literature [PDF]

Ovarian germ cell tumours (OGCTs) account for 2-5% of ovarian malignancies with an annual incidence of 1:100000 and typically occurs in young women and adolescents. A pure ovarian dysgerminoma in a postmenopausal female is a rare phenomenon.
Jaiswal, Deepshikha, Yadav, Sneh, Kalra, Irene, Sharma, Rageshwari, Gaikwad, Pradip   +4 more
core   +1 more source

Elevated serum angiotensin converting enzyme levels in metastatic ovarian dysgerminoma

, 1997
A case of a 32-year-old XY genotype female is described, presenting with mediastinal and abdominal lymphadenopathy and associated with an elevated serum angiotensin I converting enzyme (SACE) level. Lymph node histology showed a malignant dysgerminoma of
Kealy, N.P., Cotter, T.P., Bredin, C.P., Curtain, A., Duggan, P.F.   +4 more
core   +1 more source