Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer (HNPCC), is the most common cause of hereditary colorectal cancer and is caused by a germline mutation in one of the genes within the DNA mismatch repair (MMR) system. In most cases, it is most effective to first evaluate suspected Lynch syndrome with immunohistochemistry (IHC) or polymerase chain reaction (PCR) testing, as only 2-4% of colorectal cancers are Lynch syndrome associated. However, if strong suspicion exists, it is reasonable to proceed with genetic testing.
Refer to ARUP Laboratories’ test offerings below.
ARUP Laboratory Tests
Qualitative Immunohistochemistry
Qualitative Immunohistochemistry
Capillary Electrophoresis/Polymerase Chain Reaction (PCR)
Massively Parallel Sequencing
Massively Parallel Sequencing/Sequencing/Multiplex Ligation-Dependent Probe Amplification (MLPA)
Qualitative Immunohistochemistry (IHC)/Qualitative Real-Time Polymerase Chain Reaction
Qualitative Immunohistochemistry (IHC)/Qualitative Real-Time Polymerase Chain Reaction
Real-Time Polymerase Chain Reaction/Fluorescence Resonance Energy Transfer (FRET)
Massively Parallel Sequencing