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. Author manuscript; available in PMC: 2020 Jul 1.
Published in final edited form as: Fam Cancer. 2019 Jul;18(3):331–342. doi: 10.1007/s10689-019-00128-6

Table 2:

Clinical information and family history of cancer

ID Age Race Sex CRC
Locationa
Family History of Cancer
LS: MMR germline mutation
1 68 WEA F R and L Mother: breast
Father: renal cell
2 27 WEA M R Great grandmother: colon
Grandmother: colon, uterus
Great grand uncle: colon
Aunt: colon, pancreas
Cousin: colon
3 78 AA M L n/a
4 62 WEA F L n/a
5b 55 AA F R Aunt: breast
LLS: No MMR germline mutations
6 67 AA M n/a n/a
7 53 WEA M R Mother: breast
Father: prostate
8 70 AA F R Brother: esophagus
9 65 AA F R Father and brother: prostate
Sister: breast
Brother: renal cell
Aunt: neck
10 46 AA F n/a n/a
11 86 AA M R Father: brain
12 81 AA F R Mother: Uterus
13 47 WEA M R n/a
14 77 AA M R n/a
15 58 WEA M L n/a
16 50 WEA F L Mother: brain
Brother: colon

AA, African American; CRC, colorectal cancer; F, female; LLS, Lynch-like syndrome; LS, Lynch syndrome; M, male; n/a: not available, no information; WEA, White European American.

a

Tumor location is divided into tumors in the proximal colon, including the cecum, ascending colon, hepatic flexure, and transverse colon (R, right), and tumor in the distal colorectum, including the splenic flexure, descending colon, sigmoid colon, and rectum.

b

This case was seen in the University of Illinois at Chicago Familial Cancer Genetics Clinic, where she was found to have a LS mutation