Results 61 to 70 of about 7,453 (264)

Ovarian dysgerminoma with a metastasis to para‐aortic lymph node

open access: yesClinical Case Reports, 2021
We present a case of dysgerminoma of the right adnexa with an infiltration to the right wall of the uterus and a metastasis of para‐aortic lymph node.
R. Kawase, Shunji Suzuki
semanticscholar   +1 more source

Total tissue lactate dehydrogenase activity in endometrial carcinoma [PDF]

open access: yes, 2008
Lactate dehydrogenase (LDH) is essential for continuous glycolysis necessary for accelerated tumor growth. The aim of this study was to reconsider if assay of total tissue activity of this enzyme could be useful as marker for endometrial carcinoma (EC ...
Abramić, Marija   +4 more
core   +1 more source

Ovarian dysgerminoma in pregnancy

open access: yesMedicine, 2021
Rationale: Although dysgerminomas are relatively uncommon among all ovarian neoplasms, representing for only about 2%, they account for 32.8 percent of malignant ovarian germ cell tumors. Their association with pregnancy is extremely rare; due to the low
I. Sas   +3 more
semanticscholar   +1 more source

Management of germ cell tumors in children: Approaches to cure [PDF]

open access: yes, 2002
The introduction of cisplatinum chemotherapy and current advances in the surgical treatment have resulted in a dramatic improvement of the prognosis of children with malignant germ cell tumors (GCT).
Calaminus, G.   +4 more
core   +1 more source

Primary intrauterine dysgerminoma in a pregnant woman: A rare case report

open access: yesIndian Journal of Pathology and Microbiology, 2018
Primary extraovarian dysgerminoma is very rare. Nearly all reported uterine germ cell tumors are nondysgerminoma. Herein, we reported a primary intrauterine dysgerminoma.
Mojgan Akbarzadeh-Jahromi   +3 more
doaj   +1 more source

Incidental gonadal tumors at the time of gonadectomy in women with Swyer syndrome: a case series [PDF]

open access: yes, 2015
Background: Swyer syndrome (46XY complete gonadal dysgenesis) is an uncommonly encountered condition in our population. Gonadectomy is recommended upon diagnosis due to a significant risk of malignant transformation of the dysgenetic gonads, typically to
Hanlon, Amie J. M., Kimble, Rebecca M.
core   +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

Pure dysgerminoma of the ovary: CT and MRI features with pathological correlation in 13 tumors

open access: yesJournal of Ovarian Research, 2020
Background To investigate the spectrum of CT and MRI findings of dysgerminoma of the ovary. Methods CT and MRI imaging of 12 patients with 13 histologically proven dysgerminomas of the ovary were retrospectively reviewed.
S. Zhao   +7 more
semanticscholar   +1 more source

A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation [PDF]

open access: yes, 2012
Patients with Disorders of Sex Development (DSD), especially those with gonadal dysgenesis and hypovirilization are at risk of developing malignant type II germ cell tumors/cancer (GCC) (seminoma/dysgerminoma and nonseminoma), with either carcinoma in ...
Alders, M. (Mariëlle)   +14 more
core   +1 more source

Prolonged Hypercalcemia Following Resection of Dysgerminoma: A Case Report

open access: yesObstetrics and Gynecology International, 2009
Background. Hypercalcemia is a rare but potentially dangerous complication of pediatric cancer. Of the dysgerminoma cases reported to date, associated hypercalcemia is corrected within 2–7 days of tumor resection. Case.
Abigail Wald   +3 more
doaj   +1 more source

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