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Quantitation of Intra-peritoneal Ovarian Cancer Metastasis
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Ovarian angioleiomyoma: a case report.

Sun-Jae Lee1, Youn Seok Choi2, Kwan-Kyu Park1

  • 1Department of Pathology, Catholic University of Daegu College of Medicine Daegu, Republic of Korea.

International Journal of Clinical and Experimental Pathology
|January 1, 2015
PubMed
Summary

A rare ovarian tumor, angioleiomyoma (ALM), was found in a woman. This case is the third reported ovarian ALM and the first with diffuse myxoid degeneration.

Keywords:
Angioleiomyomadegenerationovary

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Area of Science:

  • Gynecologic Oncology
  • Pathology
  • Vascular Neoplasms

Background:

  • Angioleiomyoma (ALM) is a rare, benign neoplasm originating from smooth muscle cells in vascular walls.
  • ALM is exceptionally uncommon in female genital organs like the ovary.

Observation:

  • A case of a large primary ovarian angioleiomyoma in a 35-year-old woman is presented.
  • The tumor mimicked an ovarian fibroma clinically and radiologically.
  • Histological examination revealed diffuse myxoid degeneration within the angioleiomyoma.

Findings:

  • This represents the third reported case of ovarian angioleiomyoma.
  • This is the first reported case of ovarian angioleiomyoma exhibiting diffuse degeneration.

Implications:

  • Highlights the importance of considering rare neoplasms in ovarian mass differential diagnoses.
  • Adds to the limited literature on ovarian angioleiomyomas, particularly those with myxoid changes.
  • Contributes valuable data for future research on the pathology and clinical presentation of ovarian ALM.