Immunohistochemical Pitfalls: Common Mistakes in the Evaluation of Lynch Syndrome

Surg Pathol Clin. 2017 Dec;10(4):977-1007. doi: 10.1016/j.path.2017.07.012.

Abstract

At least 15% of colorectal cancers diagnosed in the United States are deficient in mismatch repair mechanisms. Most of these are sporadic, but approximately 3% of colorectal cancers result from germline alterations in mismatch repair genes and represent Lynch syndrome. It is critical to identify patients with Lynch syndrome to institute appropriate screening and surveillance for patients and their families. Exclusion of Lynch syndrome in sporadic cases is equally important because it reduces anxiety for patients and prevents excessive spending on unnecessary surveillance. Immunohistochemistry is one of the most widely used screening tools for identifying patients with Lynch syndrome.

Keywords: Immunohistochemistry; Lynch syndrome; Pitfalls; Staining pattern.

Publication types

  • Review

MeSH terms

  • Colon / pathology
  • Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis
  • Colorectal Neoplasms, Hereditary Nonpolyposis / pathology*
  • Coloring Agents
  • Humans
  • Immunohistochemistry
  • MutS Homolog 3 Protein / immunology

Substances

  • Coloring Agents
  • MutS Homolog 3 Protein