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Evaluation of Hbme-1 in the Differential Diagnosis of Reactive Mesothelial and Metastatic Adenocarcinoma Cells in Body Serous Effusions



Rahmani A1 ; Dehgani M2 ; Moghaddam NA3
Authors
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Authors Affiliations
  1. 1. Department of Gastroenterology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Pathology, School of Medicine, Banda Abbas University of Medical Sciences, Bandar Abbas, Iran

Source: Journal of Isfahan Medical School Published:2010

Abstract

Background: We tried to evaluate the diagnostic utility of HBME-1 in distinguishing between reactive mesothelial cells and adenocarcinoma in body serous effusions. Methods: We examined 52 cytologic specimens of serous effusions processed by cell block technique retrieved from the pathology archive of Al-zahra hospital (Isfahan). They were categorized in two groups: Group I. 26 effusions containing reactive mesothelial cells from patients with no evidences of malignancy based on cytomorphology, clinical data and imaging; and Group II. 26 effusions containing adenocarcinomatous cells from patients with diagnosis established by routine histology. Immunostaining with HBME-1 was performed using an Envision technique. Statistical analysis was performed with SPSS software. Findings: Statistical significance was found with HBME-1 when comparing both adenocarcinoma versus mesothelial cells (P = 0.001). Also, we found HBME-1 outlined cell membranes in reactive mesothelial cells versus cytoplasmic pattern in adenocarcinoma cells (P = 0.001). The staining intensity for adenocarcimoma cells included: Negative in 7 cases (26.9%); score + in 4 cases (15.38%), score ++ in 11 cases (42.30%) and score +++ in 4 cases (15.38%). In mesothelial cells, Negative and score + was not seen, score ++ was in 3 cases (11.5%), and score +++ in 23 cases (88.5%) (P = 0.001). Conclusion: The staining pattern and intensity for HBME-1 is a usufull panel for differentiation of adenocarcinoma and mesothelial cells. The only limitation of this marker is ovarian carcinoma that shows the same pattern as reactive mesothelial cells.