Results 51 to 60 of about 6,733 (253)

Ovarian dysgerminoma with a metastasis to para‐aortic lymph node

Clinical 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

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

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

SAGE 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, Hirotsugu Suwanai, Hironori Abe, Fumiyoshi Yakou, Takuya Ishikawa, Munehiro Urayama, Takeshi Nagai, Toshitaka Nagao, Jumpei Shikuma, Takashi Miwa, Ryo Suzuki, Masato Odawara   +11 more
doaj   +1 more source

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

, 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

Use of novel serum markers in clinical follow-up of Sertoli-Leydig cell turnours [PDF]

, 2007
Background: Sertoli-Leyclig cell tumours of the ovary account for only 0.2% of malignant ovarian tumours. Two-thirds of all patients become apparent due to the tumour's hormone production. Methods: A 41-year-old patient (gravida 4, para 4) presented with
Campisi P, Ching B, Clinton CW, Dhont M, Emons G, Gershenson DM, O'Hern TM, Prinz RA, Schwartz PE, Tampakoudis P, Young RH, Young RH, Zaloudek C   +12 more
core   +2 more sources

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

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, Baranzelli, Billmire, Billmire, Billmire, Frazier, Gershenson, Gershenson, Gobel, Grimison, Hanna, Kaplan, Kollmansberger, Lhommé, Lo Curto, Lopes, Madenci, Mangili, Mangili, Mangili, Mann, Matei, Meisel, Murray, Olson, Palenzuela, Park, Parkinson, Pashankar, Patterson, Pectasides, Rescorla, Robison, Rogers, Schemper, Schenider, Solheim, Stoneham, Travis, Vicus, Zagamè   +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, Ivan Fasulkov, Radostin Simeonov   +2 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, H. Boro, A. Goyal, R. Khadgawat
semanticscholar   +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