Original Article

Modern Pathology (2007) 20, 248–255. doi:10.1038/modpathol.3800736

D2-40 and calretinin—a tissue microarray analysis of 341 malignant mesotheliomas with emphasis on sarcomatoid differentiation

Marc Hinterberger1, Tanja Reineke1, Martina Storz1, Walter Weder2, Peter Vogt1,3 and Holger Moch1

  1. 1Department of Pathology, Institute for Surgical Pathology, University Hospital of Zurich, Zurich, Switzerland
  2. 2Department of Thoracic Surgery, University Hospital of Zurich, Zurich, Switzerland
  3. 3Pneumoconiosis Research Group, University Hospital of Zurich, Zurich, Switzerland

Correspondence: Dr H Moch, MD, Department of Pathology, Institute for Surgical Pathology, University Hospital of Zurich, Schmelzbergstrasse 12, CH-8091 Zurich, Switzerland. E-mail: holger.moch@usz.ch

Received 25 August 2006; Revised 6 November 2006; Accepted 7 November 2006.

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Abstract

Anti-calretinin antibodies are useful to differentiate adenocarcinomas from malignant mesotheliomas of the lung. Therefore, calretinin expression is rarely reported for sarcomatoid mesotheliomas. Anti-podoplanin antibodies (eg D2-40) react with lymphatic endothelia, Kaposi's sarcoma, lymphangioma and mesotheliomas. For the interpretation of spindle cell lesions of the pleura, knowledge of calretinin and D2-40 expression frequencies in sarcomatoid mesothelioma is desirable. To systematically investigate the sensitivity of calretinin and D2-40 antibodies in epithelioid and sarcomatoid areas of malignant mesotheliomas, a tissue microarray with 341 malignant mesotheliomas, including 112 epithelioid, 46 sarcomatoid and 183 biphasic tumors was constructed. Epithelioid and sarcomatoid differentiated tumor areas were clearly separated within the tissue microarray. Expression of calretinin and D2-40 was separately studied in epithelioid and sarcomatoid areas by immunohistochemistry. Calretinin expression was found in 91% of epithelioid and 57% of sarcomatoid tumor areas. D2-40 immunostaining was present in 66% of the epithelioid and 30% of the sarcomatoid tumor areas. A combination of calretinin and D2-40 increased the sensitivity in epithelioid tumor areas to 0.96 and in sarcomatoid tumor areas to 0.66. These data indicate that a combination of calretinin and D2-40 will improve diagnostic accuracy for spindle cell lesions of the pleura, whereas almost all epithelioid mesotheliomas are identified by calretinin alone.

Keywords:

M2A, podoplanin, TMA, immunohistochemistry, sensitivity, antigenetic variation

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