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An immunohistochemical approach to the diagnosis of Solid Pseudopapillary tumors of the Pancreas
  1. Stefano Serra (stefano.serra{at}uhn.on.ca)
  1. University Health Network, PMH, University of Toronto, Canada
    1. Runjan Chetty (runjan.chetty{at}uhn.on.ca)
    1. University Health Network/University of Toronto, Canada

      Abstract

      Solid pseudopapillary tumours (SPT) of the pancreas are uncommon, but with widespread and increased imaging several of these lesions are coming to light incidentally and are subject to needle biopsies. On limited material and especially the solid or clear cell variants of SPT can morphologically mimic most notably pancreatic neuroendocrine tumours and even metastatic renal cell carcinoma or melanoma. In this context, immunohistochemistry is important and useful in helping to reach the correct diagnosis.

      Several antibodies have been used in the immunohistochemical evaluation of SPT. As with most tumours, no one marker is specific but rather a core panel is advocated. Recently, both β-catenin and E-cadherin have shown to be of value in SPT. Nuclear and cytoplasmic decoration of tumour cells by β-catenin is seen almost 100% of cases. This protein relocalization from the cell membrane is underscored by mutations of the β-catenin gene. Mutations of the E-cadherin gene are very uncommon in SPT but the immunohistochemically-detected changes to the protein are consistent and present in 100% of cases. Using an E-cadherin antibody to the extracellular domain of the molecule results in complete membrane loss, while the antibody directed to the cytoplasmic fragment produces distinct nuclear staining of the tumour cells. In addition, there is concordance of staining abnormalities between the two antibodies. When combined with CD10 and progesterone receptor positivity, a diagnosis of SPT can be rendered with confidence even in small biopsy samples.

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