11 July 2026
: Case report
Rectal Adenocarcinoma With Enteroblastic Differentiation and Hepatic Metastases: A Rare and Aggressive Variant of Colorectal Carcinoma
Unusual clinical course, Mistake in diagnosis, Unusual or unexpected effect of treatment, Adverse events of drug therapy
Farzeen Fatma Syed ABCDEF 1*, Ahmed Khalid ABCDEF 2DOI: 10.12659/AJCR.953084
Am J Case Rep 2026; 27:e953084
Table 1 Immunohistochemical and molecular features supporting rectal adenocarcinoma with enteroblastic differentiation.
| Marker/feature | Rectal mass | Liver biopsy | Interpretation |
|---|---|---|---|
| SALL4 | Positive | Positive | Oncofetal/enteroblastic marker |
| MOC31 | Positive | Positive | Epithelial marker |
| BerEP4 | Positive | Not reported | Supports epithelial differentiation |
| Claudin-4 | Positive | Not reported | Supports epithelial differentiation |
| Glypican-3 | Patchy positive | Weak/patchy positive | Supports enteroblastic differentiation |
| CK7 | Not reported | Positive | Contributed to initial pancreaticobiliary impression |
| CK20 | Negative | Not reported | Loss of typical intestinal marker in rectal tumor |
| CDX2 | Negative | Focal positive on initial outside interpretation | Discordant intestinal marker staining contributed to diagnostic confusion |
| Villin | Not reported | Focal positive on initial outside interpretation | Supported initial outside interpretation |
| SATB2 | Patchy positive | Not reported | Limited support for colorectal origin |
| NKX3.1/PSA | Negative | Not reported | Argues against prostatic origin |
| PAX8/WT1 | Negative | Not reported | Argues against Müllerian/renal origin |
| GATA3 | Negative | Not reported | Argues against urothelial/breast origin |
| Synaptophysin/chromogranin | Negative | Not reported | Argues against neuroendocrine differentiation in rectal tumor |
| p40 | Negative | Negative | Argues against squamous differentiation |
| Molecular profiling (overall) | — | — | ERBB2 amplification, KRAS/NRAS wild-type status, microsatellite stability, low tumor mutational burden, and pathogenic SMAD4 and APC alterations |






