Results 31 to 40 of about 2,345 (167)

Bilateral Gonadoblastoma in a 12-Year-Old Girl 4 Years After Wilms' Tumor: A Rare Pediatric Case. [PDF]

Clin Case Rep
ABSTRACT This case of a 12‐year‐old patient who developed bilateral gonadoblastoma 4 years after treatment for Wilms tumor highlights the importance of rigorous, risk‐adapted long‐term surveillance and careful evaluation of incidental gonadal findings, even in asymptomatic patients.
Quraish A, Khouli H, Daraghmeh Y, Mosleh S, Bustame S.   +4 more
europepmc   +2 more sources

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

Archives 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, Iqra Mushtaq, Tushar Kambale, Indranil Dey   +3 more
doaj   +1 more source

Intracranial Dysgerminomas [PDF]

Canadian 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, J, Francoeur, M, Copty, C, Contreras, F, Gagne   +4 more
openaire   +2 more sources

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

Indian 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, Fatemeh Sari Aslani, Fatemesadat Najib, Shahla Hosseini   +3 more
doaj   +1 more source

Prolonged Hypercalcemia Following Resection of Dysgerminoma: A Case Report

Obstetrics 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, Sumana Narasimhan, Lucybeth Nieves-Arriba, Steven Waggoner   +3 more
doaj   +1 more source

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

Journal 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, Swati Jindal, Swati Jindal, Aruna Panchariya   +3 more
doaj   +1 more source

Dual malignancy in adolescence: A rare case report of metachronous papillary carcinoma of thyroid following dysgerminoma of ovary

Journal of Research in Medical Sciences, 2016
Dual malignancy is rare in adolescents. Dual malignancy with the second malignancy of thyroid is rare. No association has been reported between dysgerminoma of ovary and carcinoma thyroid in medical literature. Despite a thorough PubMed search (key words
Suvadip Chakrabarti, Sanjay M Desai, Dharmendra Y Mehta, Shreyas Somanath   +3 more
doaj   +1 more source

A clinical case of unilateral ovarian dysgerminoma and pyometra in a bitch [PDF]

Macedonian Veterinary Review, 2014
A clinical case of an 11-year-old bitch with unilateral ovarian dysgerminoma and pyometra is described. The owner reported purulent discharge from external genitalia, fastidious appetite and depression.
Anton Antonov, Ivan Fasulkov, Radostin Simeonov   +2 more
doaj   +1 more source

Pure ovarian dysgerminoma in a postmenopausal patient: A case report and review of the management

Gynecologic Oncology Reports, 2022
Background: A pure ovarian dysgerminoma in a postmenopausal female is a rare phenomenon. Case: A 65-year-old female presented with a large pelvic mass. Following surgical debulking, the patient was diagnosed with FIGO Stage IIB ovarian dysgerminoma.
Jennifer Vaz, Alexandra Mulliken, Nivin Omar, Jessa Suhner, Bogna Brzezinska, Thomas Cotter, Patel Nikhil, Robert V. Higgins, Bunja Rungruang   +8 more
doaj   +1 more source

A Rare Case of Ovarian Dysgerminoma with Torsion in Pregnancy [PDF]

Journal of Clinical and Diagnostic Research
Early identification of the clinical and imaging characteristics of ovarian dysgerminoma is crucial for prompt care of this rare malignant germ cell tumour, which primarily affects young women and adolescents.
Komal Rathod, Pratap Singh Parihar, Bharadwaj Saraswathula, Saburi Singhania, Yogita Rathod   +4 more
doaj   +1 more source