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. Author manuscript; available in PMC: 2019 Mar 1.
Published in final edited form as: Mod Pathol. 2018 Jun 8;31(10):1608–1618. doi: 10.1038/s41379-018-0079-6

Figure 2.

Figure 2.

This patient (Table 2, case 19) had a MSH2 and MSH6-deficient colorectal carcinoma but had negative germline MSH2, MSH6, and EPCAM mutation studies fulfilling criteria for “Lynch-like” syndrome. The patient had two solitary MSH2-deficient intestinal crypts, one of which is depicted (black arrow), that suggest Lynch syndrome despite the negative germline mutation studies (MSH2 immunohistochemistry, 100x magnification).