The frequency of dysplastic branching crypts in colorectal polypoid tubular adenomas
Rubio CA, Vieth M, Lang-Schwarz C (2023)
Publication Type: Journal article
Publication year: 2023
Journal
DOI: 10.1111/iep.12466
Abstract
Dysplastic crypt branching (DCB) was recently found in ulcerative colitis-associated dysplasia. The aim was to assess the frequency and the branching phenotype of DCB in polypoid colorectal tubular adenomas (TA). A total of 3956 DCB were found in the 139 TA: 98% were in asymmetric branching (DCAB) and the remaining 2% in symmetric branching (DCSB). A linear correlation was found between DCB frequency and the increasing digital size in TA (p <.05). Using a digital ruler, adenomas were divided into small TA (<5 mm) and larger TA (≥5 mm). The difference between the frequency of DCB in small TA (n = 75) vs. larger TA (n = 64), was significant (p <.05). DCB frequency was not influenced by age, gender or TA localization. In the normal colorectal mucosa (≈2 m2), only occasional CSB is found and no CAB. And yet, multiple DCB (mean 16.7 DCB), mostly DCAB, was found in small TA, occupying <5 mm of the mucosal area. In larger TA, as many as 42.1 DCB (mean), mostly DCAB, occurred in merely 7.8 mm (mean) of the colon mucosa. Thus it is suggested that DCB is a standard histologic element of TA. The natural expansion of the adenomatous tissue in larger TA appears to be follow on from newly produced, mostly DCAB, by DCSB and by the accumulation of their dysplastic offspring's progenies. The findings strongly suggest that DCB is a central microstructure in the histological events unfolding in polypoid colorectal TA.
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APA:
Rubio, C.A., Vieth, M., & Lang-Schwarz, C. (2023). The frequency of dysplastic branching crypts in colorectal polypoid tubular adenomas. International Journal of Experimental Pathology. https://doi.org/10.1111/iep.12466
MLA:
Rubio, Carlos A., Michael Vieth, and Corinna Lang-Schwarz. "The frequency of dysplastic branching crypts in colorectal polypoid tubular adenomas." International Journal of Experimental Pathology (2023).
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