However, CDX2 can be positive in any carcinoma that shows enteric differentiation, and thus is not entirely colorectal-specific. Interestingly, medullary carcinomas of the colorectum are frequently CK20-negative and CDX2-negative, in line with

the concept of MSI (16,19). Pathologic staging Tumor staging is by far the most important prognostic predictor of clinical outcome for patients with colorectal carcinoma. Histologic examination of surgically resected specimens serves an irreplaceable role in determining the depth Inhibitors,research,lifescience,medical of tumor invasion (T) and the extent of nodal metastasis (N). The histologic determination of T1 (tumor invades submucosa), T2 (tumor invades muscularis propria) and T3 (tumor invades through the muscularis propria into pericolorectal tissues) is usually straightforward when using the AJCC TNM staging system (9). However, determination of T4a

(tumor penetrates to the surface of the Inhibitors,research,lifescience,medical visceral peritoneum) and T4b (tumor directly invades or is adherent to other organs or structures) can sometimes be problematic. Inhibitors,research,lifescience,medical First, serosal surface (visceral peritoneum) involvement can be missed if the specimen is not adequately sampled for histologic examination. Second, the serosal surface may be confused with the circumferential (radial) or mesenteric margin, which is a nonperitonealized surface created surgically by blunt or sharp dissection. A T3 tumor may involve the {Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|buy Anti-infection Compound Library|Anti-infection Compound Library ic50|Anti-infection Compound Library price|Anti-infection Compound Library cost|Anti-infection Compound Library solubility dmso|Anti-infection Compound Library purchase|Anti-infection Compound Library manufacturer|Anti-infection Compound Library research buy|Anti-infection Compound Library order|Anti-infection Compound Library mouse|Anti-infection Compound Library chemical structure|Anti-infection Compound Library mw|Anti-infection Compound Library molecular weight|Anti-infection Compound Library datasheet|Anti-infection Compound Library supplier|Anti-infection Compound Library in vitro|Anti-infection Compound Library cell line|Anti-infection Compound Library concentration|Anti-infection Compound Library nmr|Anti-infection Compound Library in vivo|Anti-infection Compound Library clinical trial|Anti-infection Compound Library cell assay|Anti-infection Compound Library screening|Anti-infection Compound Library high throughput|buy Antiinfection Compound Library|Antiinfection Compound Library ic50|Antiinfection Compound Library price|Antiinfection Compound Library cost|Antiinfection Compound Library solubility dmso|Antiinfection Compound Library purchase|Antiinfection Compound Library manufacturer|Antiinfection Compound Library research buy|Antiinfection Compound Library order|Antiinfection Compound Library chemical structure|Antiinfection Compound Library datasheet|Antiinfection Compound Library supplier|Antiinfection Compound Library in vitro|Antiinfection Compound Library cell line|Antiinfection Compound Library concentration|Antiinfection Compound Library clinical trial|Antiinfection Compound Library cell assay|Antiinfection Compound Library screening|Antiinfection Compound Library high throughput|Anti-infection Compound high throughput screening| radial margin and a T4 tumor may have a negative radial margin. Third, a surgically induced perforation at the tumor site may be confused with true tumor perforation, which requires clarification

Inhibitors,research,lifescience,medical from surgeons. Fourth, adherence of other organs or structures at the tumor site does not necessarily qualify for T4b. Histologically, the adherent site may show only inflammatory changes, abscess formation and/or fibrosis, but without direct tumor involvement. Finally, there is some confusion about the definition of visceral peritoneum involvement. Clearly, Inhibitors,research,lifescience,medical the interpretation of T4a can be unequivocal if, (I) tumor cells are present at the serosal surface with inflammatory reaction, mesothelial hyperplasia, and/or erosion; or (II) free tumor cells are seen on the serosal surface with underlying ulceration of the visceral peritoneum. However, identification of tumor cells close to, but not at, the serosal surface would those be considered T4a by some investigators if there are associated mesothelial inflammatory and/or hyperplastic reactions (Figure 8) (22). Apparently, the application of this third criterion is prone to subjective judgment and lacks reproducibility. It is noted that in the updated cancer protocols and checklists by College of American Pathologists (CAP), only the first two criteria are listed as the diagnostic features of T4a, and the third criterion is deleted (23).