# Intussusception secondary to Peutz-Jeghers syndrome: a case report and literature review of diagnostic and therapeutic advances

**Authors:** Jing Zhang, Tian-Hao Xie, Yan Fu, Xiao-Shi Jin, Qiang Wang, Zheng Niu

PMC · DOI: 10.3389/fmed.2025.1687958 · Frontiers in Medicine · 2025-10-21

## TL;DR

A 19-year-old with Peutz-Jeghers syndrome developed intussusception due to intestinal polyps, highlighting advances in diagnosis and treatment of this rare genetic disorder.

## Contribution

The paper presents a case report and literature review emphasizing recent diagnostic and therapeutic advances in Peutz-Jeghers syndrome.

## Key findings

- Laparoscopic exploration confirmed multiple small intestinal polyps causing intussusception in a PJS patient.
- Advancements in genetic testing and endoscopic techniques improve diagnosis and management of PJS.
- Early diagnosis and lifelong surveillance are critical to reducing malignancy risks in PJS patients.

## Abstract

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant genetic disorder characterized by gastrointestinal hamartomatous polyposis and mucocutaneous pigmentation, predisposing patients to malignancies. This article reports a case of a 19-year-old male presenting with recurrent abdominal pain, diagnosed with small intestinal intussusception secondary to PJS polyps. Computed tomography revealed the “double-ring sign,” indicative of intussusception, and laparoscopic exploration confirmed multiple small intestinal polyps, which were subsequently resected. Postoperative pathology confirmed the diagnosis of PJS. The article reviews the diagnostic criteria, genetic basis, clinical manifestations, and recent advances in the management of PJS. It highlights the transformation in management strategies, driven by advancements in genetic testing, endoscopic interventions, and multidisciplinary collaboration. Early diagnosis, genetic screening for first-degree relatives, and lifelong surveillance are emphasized to mitigate the risk of malignancies and improve patient outcomes. The refinement of diagnostic criteria, genotype–phenotype correlations, and innovations in endoscopic techniques are discussed, underscoring their role in optimizing therapeutic approaches.

## Linked entities

- **Diseases:** Peutz-Jeghers syndrome (MONDO:0008280), intussusception (MONDO:0007835)

## Full-text entities

- **Diseases:** mucocutaneous pigmentation (MESH:D010859), intestinal polyps (MESH:D007417), abdominal pain (MESH:D015746), malignancies (MESH:D009369), autosomal dominant genetic disorder (MESH:D030342), polyps (MESH:D011127), Intussusception (MESH:D007443), PJS (MESH:D010580)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12583209/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12583209/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12583209/full.md

---
Source: https://tomesphere.com/paper/PMC12583209