Well-differentiated papillary mesothelioma in association with endometrial carcinoma: a case report

Vivek Rathi1, Simon Hyde, Marsali Newman

  • 1Department of Anatomical Pathology, Austin Health, Studley Road, Heidelberg 3084, Victoria, Australia. vivrathi@yahoo.com

Acta Cytologica
|November 9, 2010
PubMed
Abstract

Insights

Well-differentiated papillary mesothelioma (WDPM) is a rare peritoneal tumor. This case highlights its association with endometrial carcinoma, emphasizing diagnostic challenges and potential misinterpretations in surgical pathology.

Area of Science:

  • Gynecologic Oncology
  • Surgical Pathology
  • Cytopathology

Background:

  • Well-differentiated papillary mesothelioma (WDPM) is an uncommon peritoneal tumor.
  • Its natural history and association with other neoplasms are not well-understood.
  • WDPM is often an incidental finding during abdominal and pelvic surgery.

Observation:

  • A 62-year-old woman presented with high-grade endometrial adenocarcinoma.
  • Intraoperative findings revealed extensive peritoneal nodular fibrotic reaction.
  • Cytologic examination and peritoneal biopsies showed reactive mesothelial cells, not metastatic adenocarcinoma.

Findings:

  • The patient was diagnosed with high-grade endometrial adenocarcinoma.
  • Peritoneal biopsies confirmed well-differentiated papillary mesothelioma (WDPM).
  • This is the third reported case of WDPM associated with endometrial carcinoma.

Implications:

  • Cytologic diagnosis of WDPM can be challenging due to overlapping features with other lesions.
  • WDPM may be misdiagnosed as metastatic disease or reactive mesothelial proliferation.
  • Accurate differentiation is crucial for appropriate patient management and treatment planning.