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Benign polypoid adenomyomatous endometrium associated with hpt-JT syndrome: a case report.

Alexandra ArfiNathalie Chabbert-BuffetAnne-Sophie BoudyTiphaine de FoucherClémentine OwenSofiane BendifallahEmile Darai
Published in: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology (2019)
Hyperparathyroidism-jaw tumor (HPT-JT) is an autosomal dominant disorder responsible for benign and/or malignant tumors. Affected women often present life-threatening menorrhagia that leads to the identification of uterine tumors, and experience miscarriages and infertility. Overall though, fewer data concerning gynecological pathologies related to HPT-JT syndrome are available. We report the case of a 32-year-old woman with HPT-JT syndrome, referred for recurrent vaginal bleeding, with a history of repeated endometrial polyps and infertility. We also review the literature that explores medical options for these women.
Keyphrases
  • polycystic ovary syndrome
  • case report
  • systematic review
  • healthcare
  • pregnancy outcomes
  • atrial fibrillation
  • electronic health record
  • artificial intelligence
  • breast cancer risk
  • deep learning