Cotyledonoid dissecting leiomyoma of the uterus: report of two cases

Arch Gynecol Obstet. 2015 Feb;291(2):357-61. doi: 10.1007/s00404-014-3406-2. Epub 2014 Aug 13.

Abstract

Background: Cotyledonoid dissecting leiomyoma (Sternberg tumor) is a rare variant of the uterine smooth muscle tumor. Although this tumor is a benign tumor clinically and pathologically, the appearance and growth pattern is unusual, so it may be misdiagnosed as malignancy.

Case reports: We report two cases of cotyledonoid dissecting leiomyoma of the uterus that occurred in two 44- and 31-year-old women, respectively. Total hysterectomy and bilateral salpingo-oophorectomy were performed in one of the patients, and myomectomy was done in the other one. Macroscopically, both tumors were grape-like exophytic masses resembling placental tissue. The patients were well after surgery, and one patient gave birth. To our knowledge, this is the first case report of a successful delivery after myomectomy of this tumor.

Conclusion: To prevent aggressive surgery it is important to recognize that this tumor is a benign and unusual appearing variant of leiomyoma. A fertility-sparing surgical procedure should be considered if the patient wishes to preserve her fertility.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Fallopian Tubes / surgery
  • Female
  • Humans
  • Hysterectomy / methods
  • Leiomyoma / pathology
  • Leiomyoma / surgery*
  • Ovariectomy / methods
  • Pregnancy
  • Smooth Muscle Tumor / pathology
  • Smooth Muscle Tumor / surgery*
  • Uterine Myomectomy / methods
  • Uterine Neoplasms / pathology
  • Uterine Neoplasms / surgery*