Modified Liquid-Based Cytology Technique for Immunocytochemistry in Effusion Specimen

Natcha Patarapadungkit1, Porntip Jangsiriwitayakorn1, Surachat Chaiwiriyakul1

  • 1Department of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Insights

A modified liquid-based cytology technique enhances immunocytochemistry for serous effusions. This method effectively differentiates metastatic adenocarcinoma from benign mesothelium using a panel of markers.

Area of Science:

  • Cytopathology
  • Oncology
  • Immunohistochemistry

Background:

  • Immunocytochemistry (ICC) of serous effusions is crucial for diagnosing benign and malignant cells.
  • Accurate differentiation between metastatic adenocarcinoma and benign mesothelium is clinically significant.

Purpose of the Study:

  • To develop and evaluate a modified liquid-based cytology (LBC) technique for ICC of serous effusions.
  • To assess the efficacy of a specific marker panel in distinguishing metastatic adenocarcinoma from benign mesothelium.

Main Methods:

  • A modified LBC technique was applied to 110 serous effusion cases (50 benign, 60 metastatic adenocarcinoma).
  • Immunocytochemistry was performed using a panel of markers: EMA, Ber-EP4, Calretinin, and p63.
  • Cytological preparations were interpreted by a cytotechnologist and a pathologist, with comparative analysis of results.

Main Results:

  • Metastatic adenocarcinoma cases showed 100% positivity for EMA and 91.7% for Ber-EP4, while being negative for Calretinin and p63.
  • Benign mesothelium cases were 100% positive for Calretinin and negative for carcinoma markers.
  • The diagnostic differentiation based on ICC was statistically significant (p < 0.001).

Conclusions:

  • A marker panel including EMA, Ber-EP4, and Calretinin effectively differentiates metastatic adenocarcinoma from benign mesothelium in serous effusions.
  • The modified LBC technique provides an effective specimen preparation for ICC analysis in serous effusions.
  • This approach improves diagnostic accuracy in the cytopathological evaluation of serous effusions.