Results 61 to 70 of about 7,611 (271)
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 +3 more
doaj +1 more source
Swyer syndrome (46, XY complete gonadal dysgenesis): A rare case of primary amenorrhea
Philippine 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
Ovarian dysgerminoma in pregnancy
Medicine, 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
Malignant ovarian germ cell tumors in pediatric patients: The AIEOP (Associazione Italiana Ematologia Oncologia Pediatrica) study [PDF]
, 2017 Objective: Malignant ovarian germ cell tumors (MOGCT) carry an excellent prognosis, and the treatment aims to achieve results with the least possible treatment-related morbidity. The aim of this study was to assess the outcomes of pediatric patients with
Amsalem +40 more
core +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 +2 more
doaj +1 more source
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 +3 more
doaj +1 more source
Cromossomo Y na síndrome de Turner: revisão da literatura [PDF]
, 2009 Turner syndrome (TS) is one of the most common types of aneuploidy among humans, and is present in 1:2000 newborns with female phenotype. Cytogenetically, the syndrome is characterized by sex chromosome monosomy (45,X), which is present in 50-60% of the ...
Bianco, Bianca Alves Vieira +5 more
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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 +8 more
doaj +1 more source
46, XY complete gonadal dysgenesis with pubertal virilisation due to dysgerminoma/gonadoblastoma
BMJ Case Reports, 2020 Complete gonadal dysgenesis (CGD) or Swyer syndrome is characterised by sexual infantilism in a phenotypic female with 46, XY karyotype. Patients with gonadal dysgenesis and Y-chromosome material are at a high risk of developing gonadoblastoma and ...
S. Alam +3 more
semanticscholar +1 more source
Open Journal of Obstetrics and Gynecology, 2021 Background: Dysgerminoma is a germ cell tumor of the ovary usually found in young women. It represents 1% to 2% of all ovarian cancers. The preoperative diagnosis is generally difficult.
B. Douaguibe +9 more
semanticscholar +1 more source