Well-differentiated papillary mesothelioma in the pelvic cavity. A case report

Tomoko Haba1, Kenichi Wakasa, Masaomi Sasaki

  • 1Department of Pathology, Osaka City University Hospital, 1-5-7, Asahi-machi, Abeno-ku, Osaka City, Osaka, 545-8586, Japan.

Acta Cytologica
|February 15, 2003
PubMed
Abstract

Insights

Well-differentiated papillary mesothelioma (WDPM) is a rare peritoneal tumor often found incidentally. Accurate cytologic differentiation from malignant mesothelioma is crucial for appropriate patient management.

Area of Science:

  • Oncology
  • Cytopathology

Background:

  • Well-differentiated papillary mesothelioma (WDPM) is a distinct subtype of peritoneal mesothelioma.
  • Typically observed in young women, WDPM is often incidentally discovered during surgery for other conditions.
  • Clinically, WDPM is generally considered benign or of low malignant potential.

Observation:

  • A 48-year-old female presented with hypermenorrhea and underwent surgery for adenomyosis.
  • Six small papillary nodules (<2 cm) were identified on the pelvic serosa.
  • Cytologic examination of peritoneal lavage and tumor imprints was performed.

Findings:

  • Cytologic specimens revealed scattered cells and clusters with abundant cytoplasm, distinct borders, and slit-like intercellular spaces.
  • Cells exhibited uniform nuclei with a single nucleolus, lacking binucleation or mitotic activity.
  • A brush border was noted on the luminal cell surfaces, characteristic of mesothelial origin.

Implications:

  • Accurate cytologic diagnosis is essential to distinguish WDPM from diffuse malignant mesothelioma.
  • Misdiagnosis can lead to unnecessary aggressive treatment for a potentially benign condition.
  • This case highlights key cytologic features for identifying WDPM.