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The aim of this retrospective multicentric case series is to describe the CT findings of ovarian neoplasia in dogs. Twenty dogs with pre- and postcontrast CT exams and cytological/histological diagnosis of ovarian neoplasia were included. Five dogs presented with bilateral tumors, for a total of 25 neoplasms: 15 carcinomas (4 bilateral), 4 granulosa cell tumors, 2 poorly differentiated malignant neoplasia (bilateral), 2 luteomas, 1 teratoma, 1 dysgerminoma.

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Intermittent severe abdominal pain is a medical emergency with multiple possible underlying causes. This case report describes a 30-year-old female experiencing severe pelvic pain alternating between the left and right lower abdomen. The pain was periodic and very intense.

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A Case of Dysgerminoma in a Pediatric Patient With a PIK3CD Mutation.

Urology

August 2024

Department of Pediatrics, Division of Pediatric Urology, Wake Forest University School of Medicine, Atrium Health Levine Children's Hospital, Charlotte, NC.

Article Synopsis
  • - Dysgerminoma is a rare type of germ cell tumor found mostly in young females, often causing abdominal pain and swelling, with surgery being the primary treatment method, followed by chemotherapy for advanced stages.
  • - The presence of specific genetic factors, like the SRY gene and dysgenic gonads, can increase the risk of unusual presentations of dysgerminoma, although clear links to other genetic mutations remain uncertain.
  • - The article examines a unique case of dysgerminoma in a young patient with genetic anomalies, while also covering the tumor's epidemiology, diagnosis, treatment options, and possible genetic mutations linked to dysgerminoma.
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Ovary dysgerminoma is one of the most good prognosis malignant tumor, which has a 5-year overall survival rate exceeding to 90%. Generally, the incidence of ovarian dysgerminoma (OD) is relatively low, accounting for ~0.6% of all ovarian tumors.

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Sclerosing stromal tumors are a rare type of ovarian tumor in the category of sex cord stromal tumors, which arise from the ovarian connective tissue. This report concerns a case of a sclerosing stromal tumor in a 19-year-old nulliparous woman who presented with the chief complaints of menstrual irregularities and dyspareunia. Preoperative imaging revealed a complex right adnexal mass with blood flow and without associated ascites.

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