Gastrointestinal Bleeding in the Setting of Juvenile Polyposis Syndrome Due to SMAD4 Mutation.
Paula Marincola SmithMarcus C TanPublished in: The American surgeon (2023)
A 27-year-old female presented at 13 weeks' gestation with epigastric pain and anemia requiring blood and iron transfusions but no family history of gastrointestinal malignancy. Upper endoscopy revealed a giant circumferential polyp and associated hyperplastic-appearing polyps in the proximal stomach. Biopsies revealed hyperplasia with lamina propria eosinophils. She was supported with intermittent transfusions until labor was induced at 34 weeks' gestation. Total gastrectomy was performed at seven weeks post-partum. Final pathology revealed multiple hamartomatous polyps without malignancy. Her anemia resolved postoperatively. Genetic testing revealed mutation of the SMAD4 gene and Juvenile Polyposis Syndrome. JPS is caused by germline mutations in the SMAD4 or BMPR1A genes and is characterized by hamartomatous polyps in the gastrointestinal tract. While most polyps are benign, malignant transformation can occur. One should have low threshold to send patients for genetic screening when multiple polyps are found in a young patient, even without family history.
Keyphrases
- chronic rhinosinusitis
- gestational age
- end stage renal disease
- chronic kidney disease
- single cell
- epithelial mesenchymal transition
- transforming growth factor
- genome wide
- case report
- iron deficiency
- preterm infants
- newly diagnosed
- chronic pain
- ejection fraction
- prognostic factors
- pain management
- preterm birth
- high glucose
- dna methylation
- dna repair
- peritoneal dialysis
- genome wide identification
- high intensity
- endothelial cells
- dna damage
- middle aged