Results 121 to 130 of about 5,696 (226)

A Case of True Hemaphroditism Presenting with Dysgerminoma [PDF]

open access: yes, 2017
The true hermaphroditism represents only 5% of all disorders of sexual differentiation, thus it is one of the rarest varieties. Diagnosis of true hermaphroditism requires the presence of both ovary and testis either as separate organs or combined to form
Umesh Babu Sharma   +4 more
core   +1 more source

Swyer Syndrome: Clinical Case of Gonadal Dysgenesis in a 15-year-old Girl

open access: yesПедиатрическая фармакология
Swyer syndrome is a rare genetic disorder in which gonadal dysgenesis and karyotype 46, XY are observed. In the postnatal and prepubescent period, this disease has no clinical manifestations and is asymptomatic, which makes diagnosis difficult. The first
Irina V. Karachentsova   +7 more
doaj   +1 more source

Hypercalcemia Due to Paraneoplastic Production of 1,25- Dihydroxyvitamin D in a Young Female with Dysgerminoma

open access: yesCureus, 2019
Humoral hypercalcemia of malignancy (HHM) can be caused by ectopic paraneoplastic production of 1, 25 dihydroxy vitamin D due to the hyperactivity of the 1 alpha-hydroxylase enzyme.
Iqra Iqbal   +4 more
semanticscholar   +1 more source

Treatment of bilateral ovarian dysgerminoma with 11-year follow-up: A case report

open access: yesAnnals of Medicine and Surgery, 2018
Introduction Malignant ovarian germ cell tumors (MOGCTs) are rare malignancies with an incidence of about 0.5/100,000. They account for less than 5% of all ovarian tumors, of which 32.8% are dysgerminomas, the female analogue of seminomas.
L. Zogbi   +8 more
semanticscholar   +1 more source

Torsion of Ovarian Dysgerminoma in a Child: Role of Computed Tomography

open access: yesCureus, 2018
Dysgerminomas are malignant germ cell tumors of the ovary that most commonly occur in the adolescent population. Ovarian dysgerminoma presenting with complications like torsion is a rare entity in the pediatric age group.
Kumail Khandwala   +3 more
semanticscholar   +1 more source

Ovarian dysgerminoma. A clinico-pathologic study.

open access: yes, 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  

Study of germ cell tumors of ovary and associated immunohistochemistry [PDF]

open access: yesJournal of Clinical and Basic Research
Background: Females have a 6–7% lifetime risk of developing ovarian tumors. Ovarian cancer is often termed a “silent killer” due to its frequent diagnosis at advanced stages.
Devunoori Sagarika   +6 more
doaj  

Treatment Results of Ovarian Dysgerminoma

open access: yes, 1996
Purpose: We tried to evaluate the clinical characteristics, the treatment methods, the results of treatments, and the patterns of failure in ovarian dysgerminoma retrospectively.
금기창, 성진실
core  

Dysgerminoma: a case report on rare malignant tumor [PDF]

open access: yes
Dysgerminoma is a malignant germ cell tumour (GCT) accounting for less than 1% of ovarian neoplasm. It is analogous to seminoma in males. It is a tumour of young age, affecting women of reproductive age group.
Anand, Mamta Neelesh   +2 more
core   +1 more source

Dysgerminoma [PDF]

open access: yesPostgraduate Medical Journal, 1967
openaire   +2 more sources

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