# Colorectal cancer in a man with silver-Russell syndrome: a case report

**Authors:** Farah Ibraik, Ibraheem Hammouri, Hasan Arafat, Ahmad G Hammouri, Hanna Qahoush

PMC · DOI: 10.1093/omcr/omaf204 · Oxford Medical Case Reports · 2025-10-29

## TL;DR

A 31-year-old man with Silver-Russell syndrome was diagnosed with colorectal cancer, a previously unreported association.

## Contribution

This case report is the first to document colorectal cancer in a patient with Silver-Russell syndrome.

## Key findings

- A 31-year-old man with Silver-Russell syndrome was found to have moderately differentiated adenocarcinoma.
- Staging revealed multiple lung and hepatic nodules, indicating cancer spread.
- This case highlights a potential but previously unreported link between SRS and colorectal cancer.

## Abstract

Silver-Russell syndrome (SRS), also known as Russell-Silver syndrome (RSS), is a congenital growth disorder characterized by intrauterine and postnatal growth retardation, craniofacial disproportion, asymmetry, and other distinctive features. It was first described by Alex Russell and Henry Silver in the 50s of the 20th century. Its broad range of manifestations makes its true incidence difficult to determine. While gastrointestinal anomalies such as gastroesophageal reflux disease and esophagitis have been reported in SRS patients, an association with colorectal cancer (CRC) has not been described. Here, we present the case of a 31-year-old man with SRS who was referred to us for constipation. A rectal biopsy revealed moderately differentiated adenocarcinoma, and a staging CT scan demonstrated multiple lung and hepatic nodules.

## Linked entities

- **Diseases:** Silver-Russell syndrome (MONDO:0008394), colorectal cancer (MONDO:0005575), gastroesophageal reflux disease (MONDO:0007186), esophagitis (MONDO:0001409)

## Full-text entities

- **Diseases:** asymmetry (MESH:D005146), adenocarcinoma (MESH:D000230), CRC (MESH:D015179), craniofacial disproportion (MESH:D020914), congenital growth disorder (MESH:D006130), RSS (MESH:D056730), intrauterine (MESH:D005317), gastroesophageal reflux disease (MESH:D005764), constipation (MESH:D003248), esophagitis (MESH:D004941), gastrointestinal anomalies (MESH:D005767)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12570015/full.md

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Source: https://tomesphere.com/paper/PMC12570015