Immunocytochemical staining of serous effusions: an additional method in the routine cytology practice?

M Lidang Jensen1, P Johansen

  • 1Department of Pathology, Aalborg Hospital, Denmark.

Insights

Immunocytochemistry using Ber-EP4 and EMA aids in diagnosing malignant serous effusions. This method, when combined with cytomorphology, improves cancer detection but requires careful interpretation to avoid false positives.

Area of Science:

  • Cytopathology
  • Immunocytochemistry
  • Oncology

Background:

  • Serous fluid analysis is crucial for diagnosing various conditions, including malignancy.
  • Traditional cytomorphology can sometimes be insufficient for definitive diagnosis in serous effusions.
  • Immunocytochemistry offers potential for improved diagnostic accuracy.

Purpose of the Study:

  • To evaluate the utility of a panel of antibodies, specifically Ber-EP4 and EMA, in differentiating benign from malignant cells in serous fluids.
  • To assess the impact of immunocytochemistry on the detection rate of malignant cases in serous effusions.
  • To establish reliable immunocytochemical staining profiles for accurate diagnosis.

Main Methods:

  • A prospective study involving 100 serous fluid samples.
  • Cytomorphologic analysis combined with immunocytochemistry using a panel of antibodies, including Ber-EP4 and Epithelial Membrane Antigen (EMA).
  • Classification of staining patterns into benign and malignant profiles.

Main Results:

  • Three distinct immunocytochemical staining profiles were identified: benign (negative for Ber-EP4/CEA), malignant epithelial (Ber-EP4 and EMA positive), and malignant mesothelial (EMA positive).
  • Application of these profiles increased the recognition of malignant cases from 19 to 38.
  • Two cases showed a false-positive malignant epithelial profile, highlighting the need for correlation with other data.

Conclusions:

  • Immunocytochemistry with anti-Ber-EP4 and anti-EMA is a valuable addition to routine cytomorphologic analysis of serous fluids.
  • This approach significantly enhances the detection of malignancy in serous effusions.
  • Results must be correlated with cytomorphology, histology, and clinical information for accurate interpretation and to mitigate false positives.

Related Concept Videos

Immunofluorescence Microscopy01:12

Immunofluorescence Microscopy

A fluorescence microscope uses fluorescent chromophores called fluorochromes, which can absorb energy from a light source and then emit this energy as visible light. Fluorochromes include naturally fluorescent substances (such as chlorophylls) and fluorescent stains that are added to the specimen to create contrast. Dyes such as Texas red and FITC are examples of fluorochromes. Other examples include the nucleic acid dyes 4’,6’-diamidino-2-phenylindole (DAPI), and acridine orange.
The...
Immunocytochemistry and Immunohistochemistry01:22

Immunocytochemistry and Immunohistochemistry

Immunocytochemistry (ICC) and immunohistochemistry (IHC) are techniques that use antibodies to check for specific proteins or antigens in a sample. The technique was first published by Albert Coons in 1941 to detect the presence of pneumococcal antigen in tissue sections from mice infected with Pneumococcus. Immunocytochemistry helps localization of proteins or antigens in individual cells like blood cells, stem cells, etc., while immunohistochemistry does the same for tissue samples.
These...
Immunogold Electron Microscopy01:20

Immunogold Electron Microscopy

Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.