Organ
|
Histology
|
Immunohistochemistry
|
Mutation
|
MSI
|
---|
p53
|
Nuclear β-catenin
|
KRAS
|
BRAF
|
---|
Esophagus 1
|
SCC
|
+
|
–
|
Wt
|
Wt
|
MSS
|
Esophagus 2
|
SCC
|
–
|
–
|
Wt
|
Wt
|
MSS
|
Stomach 1
|
AC
|
+
|
–
|
Wt
|
Wt
|
MSS
|
Ear canal
|
SCC
|
–
|
–
|
Wt
|
Wt
|
MSS
|
Esophagus 3
|
SCC
|
–
|
–
|
Wt
|
Wt
|
MSS
|
Rectum
|
AC
|
+
|
+
|
G12C
|
Wt
|
MSS
|
Stomach 2
|
AC
|
–
|
–
|
G12C
|
Wt
|
MSS
|
Prostate
|
AC
|
–
|
–
|
Wt
|
Wt
|
MSS
|
Colon
|
AC
|
–
|
+
|
G13 V
|
Wt
|
MSS
|
- The histologic, immunohistochemical (p53, β-catenin), and mutational analysis (KRAS, BRAF, and microsatellite status) characteristics of surgically and endoscopically removed tumor tissues from a man diagnosed with nine metachronous primary malignant lesions
- SCC, squamous cell carcinoma; AC, adenocarcinoma; Wt, wild type; MSI, microsatellite instability; MSS, microsatellite stable