Results 21 to 30 of about 6,733 (253)

Ovarian dysgerminoma: clues to the radiological diagnosis

open access: yesDiagnostic and Interventional Radiology, 2023
Ovarian dysgerminoma (OD) is a rare germ cell tumor accounting for 1%–2% of all malignant ovarian tumors and is generally associated with a good prognosis.
S. Amante, A. Félix, T. Cunha
semanticscholar   +1 more source

Ovarian Dysgerminoma – Challenging Presurgical Diagnosis and Mini-Mally Invasive Treatment

open access: yesArchives of Clinical and Medical Case Reports, 2023
Dysgerminoma is a rare malignant germ cell tumor of the ovary that often affects women in reproductive age. The presurgical differentiation of dysgerminoma from benign conditions is challenging. In early stages, malignant dysgerminoma can be treated with
O. K   +5 more
semanticscholar   +1 more source

Swyer Syndrome Presenting as Dysgerminoma: A Case Report

open access: yesJournal of the ASEAN Federation of Endocrine Societies, 2023
Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but with the presence of typical Müllerian structures in a phenotypically female individual.
S. Tarenia   +7 more
semanticscholar   +1 more source

Management of malignant dysgerminoma of the ovary

open access: yesEuropean Journal of Gynaecological Oncology, 2022
The evolution of treatment for malignant ovarian germ cell tumors has been one of the most successful in the history of gynecologic oncology, with dysgerminoma as the most common type of malignant ovarian germ cell tumors.
Tjadina Arndt   +6 more
semanticscholar   +1 more source

Paediatric Ovarian Dysgerminoma: A Case Report

open access: yesJNMA; journal of the Nepal Medical Association, 2022
Dysgerminoma is the most common malignant germ cell tumour of the ovary. Abdominal pain, abdominal distention, and the presence of a palpable mass are common symptoms at presentation. This is usually detected in youth, before the age of 20 years. Ovarian
Siddhant Adhikari   +2 more
semanticscholar   +1 more source

Anaplastic dysgerminoma [PDF]

open access: yesCancer, 1978
A rare case of rapidly evolving dysgerminoma produced death by tumor in less than two months after onset of symptoms. It is important to recall that dysgerminoma possesses considerable malignant potential, which infrequently is manifested by rapidly progressive disease.
J J, Gillespie, L K, Arnold
openaire   +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

Intracranial Dysgerminomas [PDF]

open access: yesCanadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 1976
SUMMARY:We have reported three cases of intracranial dysgerminoma. The origin of these tumors has been controversial for a long time. It is now accepted that they develop from germ cells. The diagnosis is often difficult to confirm because of the variety of signs.
G, Leblanc   +4 more
openaire   +2 more sources

An Incidental Finding of Bilateral Dysgerminoma During Cesarean Section: Dilemmas in Management [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Dysgerminoma is an uncommon malignant tumour arising from germ cells of ovary. It occurs mostly in the reproductive age group. Its association with pregnancy is rare. Its management remains a challenge especially in an unsuspected case.
Mamta Gupta, Rita Jindal, Vandana Saini
doaj   +1 more source

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