Results 31 to 40 of about 3,154 (149)

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

Case Report: Ovarian dysgerminoma with pseudo-Meigs syndrome in a child. [PDF]

open access: yesFront Pediatr
Ovarian dysgerminoma is a rare pediatric germ cell tumor, and its association with pseudo-Meigs syndrome (PMS) is exceedingly uncommon. PMS is characterized by massive pleural effusions and ascites accompanying a pelvic mass, which often leads to ...
Li Z, Chen D, Wei Q.
europepmc   +2 more sources

Dysgerminoma and pregnancy [PDF]

open access: yes, 2017
Introduction. Dysgerminomas are germ cell ovarian tumors. They affect young females, prevalently during childhood. The problem arises when dysgerminoma is diagnosed in women of reproductive age who have never given birth and require a surgical procedure.
Trenkić Milan   +4 more
core   +2 more sources

Dysgerminoma and gonadoblastoma in the course of Swyer syndrome [PDF]

open access: yes, 2016
We present a case of a woman with primary amenorrhea. Ultrasound imaging showed a uterus of normal size but bands of connective tissues at the site of ovaries. A genetic test was done which revealed the XY karyotype. Swyer syndrome was diagnosed.
Andrzej Wojtyś   +19 more
core   +1 more source

Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas. [PDF]

open access: yesPLoS ONE, 2012
Activating c-KIT mutations (exons 11 and 17) are found in 10-40% of testicular seminomas, the majority being missense point mutations (codon 816). Malignant ovarian dysgerminomas represent ~3% of all ovarian cancers in Western countries, resembling ...
Remko Hersmus   +12 more
doaj   +1 more source

Swyer syndrome (46XY pure gonadal dysgenesis) presenting with dysgerminoma

open access: yesArchives of Medicine and Health Sciences, 2019
Dysgerminoma is the most common malignant germ cell tumor of the ovary. This malignancy can be associated with pure gonadal dysgenesis (Swyer syndrome), mixed gonadal dysgenesis, and partial gonadal dysgenesis. Dysgerminoma usually develops in phenotypic
M Banyameen Iqbal   +3 more
doaj   +1 more source

Swyer syndrome (46, XY complete gonadal dysgenesis): A rare case of primary amenorrhea

open access: yesPhilippine Journal of Obstetrics and Gynecology, 2022
Swyer syndrome is a type of gonadal dysgenesis wherein a 46, XY karyotype presents with a female phenotype. It is a rare cause of disorder in sexual development that occurs in 1:100,000 births. Local studies are currently limited to few case reports. Sex-
Pamela Maria P. Mallari   +1 more
doaj   +1 more source

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

open access: yesSAGE 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
Natsuko Hara   +11 more
doaj   +1 more source

Histomorphological Spectrum of Gonadal and Extragonadal Germ Cell Tumours at a Tertiary Cancer Centre in Southern Rajasthan, India [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2021
Introduction: Germ Cell Tumours (GCT) are heterogenous tumours believed to arise from primordial germ cells. The GCT predominantly affects gonads (testis and ovary) and also involves extragonadal sites, characteristically locations along midline of ...
Tarang Patel   +3 more
doaj   +1 more source

46XX pure gonadal dysgenesis with dysgerminoma along with leydig cells: a unique presentation [PDF]

open access: yes, 2020
Authors report a unique case of 46XX gonadal dysgenesis, with dysgerminoma in one ovary and other streak ovary with hilar nests of leydig cells. It is exceptionally rare to find dysgerminoma in a dysgenetic gonad with no Y chromosome and so is the ...
Singh, Pratibha   +3 more
core   +1 more source

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