Aims:
The targets of this study are to describe postcolonoscopy colorectal cancer (PCCRC)
histopathological features and to evaluate relevant differences between PCCRC and
sporadic colorectal cancer (SCRC) in this topic.
Methods:
A retrospective simple centre study in a Universitary Hospital was carried out. Colorectal
cancer (CRC) cases diagnosed for three years period were revised (n = 291). PCCRC
cases were identified (n = 17; 6 – 60 months after a negative colonoscopy). Statistically
significant differences regarding histological type in both groups were analysed (PCCRC
vs. SCRC). To value histopathological differences, PCCRC cases and a SCRC control
group were paired (1:1) regarding histological type, tumoral grade, tumour stadium
and location. Features related with CRC prognosis were re-examined by an expert pathologist
(lymphatic, vascular and perineural invasion, budding tumour mayor than 10, tumoral
grown type, peritumoral lymphoid inflammatory infiltration grade, lymphoid Crohn type
response and Tumour Intraepithelial lymphocytes. Statistical analysis: Pearson X2 test for qualitative variables.
Results:
Serrated adenocarcinoma and High-Microsatellite Instability Carcinoma (MSI-H) were
more frequent in PCCRC group tan in SCRC (23.53% and 11.76% versus 14.57% and 2.21%
respectively), but differences were not significant. All cases of PCCRC had an inflammatory
infiltration (High or Low grade) versus 58.83% in SCRC control group (p = 0.011).
Lymphoid Crohn type response was present in 47% of PCCRC cases versus 5.88% of SCRC
control group (p = 0.007) (Table 1). There were no statistical differences in the
other histopathological features.
Conclusions:
There are few studies in the literature that analyse PCCRC pathological features.
There are some references to molecular aspects. Studies about histopathological characteristics
described above have not been found. Predominating Inflammatory infiltration and lymphoid
Crohn type response are histopathological features observed in PCCRC with significant
difference. Further studies are necessary to extrapolate results observed in this
study.