1,721,051 research outputs found
Hereditary non-BRCA gynecological tumors
Early diagnosis and proper management of gynecologic malignancies represent a challenge in modern oncology. A growing interest has arisen around the gynecological manifestations of hereditary cancer syndromes. In particular, the discovery of the BRCA1 and BRCA2 genes in ovarian cancer and the mismatch repair genes (MMR) in endometrial carcinoma has revolutionized our approach to the diagnosis and screening of women for ovarian and uterine cancers. The clinical, genetic and pathological features of hereditary cancer syndromes with gynecological manifestations are reviewed focusing on Lynch Syndrome, also known as Hereditary Nonpolyposis Colorectal Carcinoma (HNPCC), Peutz-Jeghers Syndrome, Cowden Syndrome or Multiple Hamartoma Syndrome, Gorlin Syndrome or Nevoid basal-cell carcinoma syndrome (NBCCS) and Reed's Syndrome or Hereditary leiomyomatosis and renal cell cancer (HLRCC)
Placental Pathology And Sars-Cov-2 Infection: The Experience And The Management Of A Regional Referral Center
Rectal water-contrast transvaginal ultrasonography versus sonovaginography for the diagnosis of posterior deep pelvic endometriosis: a prospective comparative study
Preoperative treatment with leuprolide acetate and ulipristal acetate before outpatient hysteroscopic myomectomy: prospective comparative study
Magnetic resonance with gel enema (MR-e) versus computed tomographic colonography (CTC) for diagnosing rectosigmoid endometriosis
EP02. 24: Placental structure and blood flow in pregnancies achieved using homologous versus heterologous oocytes
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