Results 21 to 30 of about 3,154 (149)

Dysgerminoma with Pregnancy and Viable Baby: A Case Report

open access: yesOman Medical Journal, 2011
Dysgerminomas are the most common of primitive germ cell tumors of the ovary, accounting for 1-5% of all ovarian malignancies. The reproductive age group females are most commonly affected, thereby causing problems in conception and if pregnancy occurs ...
Kafil Akhtar   +3 more
doaj   +3 more sources

Cranial and intra-axial metastasis originating from a primary ovarian Dysgerminoma

open access: yesGynecologic Oncology Reports, 2019
Dysgerminomas are aggressive germ cell tumors that typically have a favorable prognosis, especially in patients diagnosed with early stage disease. We recount the history of a 23-year-old woman who was treated for a stage IA ovarian dysgerminoma in ...
Tiffany L. Beck   +5 more
doaj   +2 more sources

Stage IIIC Bilateral Dysgerminoma in 46,XY Swyer Syndrome: Preventing Malignancy Through Early Endocrine Evaluation of Primary Amenorrhea. [PDF]

open access: yesClin Case Rep
Clinical Case Reports, Volume 14, Issue 7, July 2026.
Elendu C   +4 more
europepmc   +2 more sources

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

open access: yesClin Case Rep
ABSTRACT 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. Diagnosis was based on classical histopathology.
Khaniya B   +5 more
europepmc   +2 more sources

Ovarian dysgerminoma: a case report [PDF]

open access: yes, 2021
An ovarian dysgerminoma is a rare, malignant tumour occurring in young women, accounting for 1% to 2% of all primary ovarian neoplasms. A 22 years old female presented with 6 months of amenorrhea and lump in the abdomen.
Wakode, Shamrao Ramji   +3 more
core   +1 more source

Malignant Ovarian Germ Cell Tumor-Survival and Reproductive Outcomes and Patterns of Relapse. [PDF]

open access: yesCancer Med
BLURB FOR ETOC: Patients presenting with advanced MOGCT can be offered fertility‐sparing surgery after neoadjuvant chemotherapy with no detriment in oncological outcome. ABSTRACT Background Malignant ovarian germ cell tumors [MOGCT] are rare cancers affecting young women and often present in advanced stages.
Dey S   +24 more
europepmc   +2 more sources

Clinical Features of Malignant Ovarian Germ Cell Tumors According to Demographic and Pathologic Characteristics. [PDF]

open access: yesHealth Sci Rep
ABSTRACT Background and Aims Malignant ovarian germ cell tumors (MOGCTs) are aggressive cancers affecting mainly young women, in whom fertility preservation is important. Diagnosis is often delayed because early symptoms are non‐specific, leading to advanced disease or emergency surgery that may limit optimal staging and fertility‐sparing treatment. As
Agah J   +3 more
europepmc   +2 more sources

A successful spontaneous pregnancy after surgery and chemotherapy in a patient with recurrent dysgerminoma: A case report

open access: yesPhilippine Journal of Obstetrics and Gynecology, 2022
Dysgerminoma comprises 3%–5% among ovarian malignancies, mostly seen in adolescent and early adult women. The recurrence rate is approximately 10%–20%, occurring within 2 years of diagnosis, and has been reported that more than 75% occur in the 1st year.
Amor Mae M. Pasigon, Jimmy A. Billod
doaj   +1 more source

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   +1 more source

An aggressive systemic mastocytosis preceded by ovarian dysgerminoma

open access: yesBMC Cancer, 2020
Background Aggressive systemic mastocytosis (ASM) is a rare malignant disease characterized by disordered mast cell accumulation in various organs. We here describe a female ASM patient with a previous history of ovarian dysgerminoma.
Makiko Tsutsumi   +10 more
doaj   +1 more source

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