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Management of hyperplastic gastric polyp following upper gastrointestinal bleeding in infant with Menkes' disease
Dalia Belsha1, Priya Narula1, Arun Urs1
1Dalia Belsha, Priya Narula, Arun Urs, Mike Thomson, Centre of Paediatric Gastroenterology, Sheffield Children's Hospital, Sheffield S10 2TH, United Kingdom.
Insights
This case study details an infant with Menkes
Area of Science:
- Gastroenterology
- Pediatric Medicine
- Medical Genetics
Background:
- Menkes' disease (MD) is a rare genetic disorder affecting copper metabolism.
- Gastrointestinal manifestations, though reported, are less common.
- Early diagnosis and management are crucial for patient outcomes.
Observation:
- A five-month-old infant presented with severe upper gastrointestinal bleeding (coffee ground vomiting, melaena) and anemia.
- Endoscopic evaluation revealed a large, bleeding, trans-pyloric polyp.
- The infant had a confirmed diagnosis of Menkes' disease.
Findings:
- Endoscopic mucosal resection using a grasp-and-snare technique successfully removed the polyp.
- Argon plasma coagulation achieved hemostasis, and no perforation occurred.
- Complete excision after repeated debridement resolved bleeding without further transfusions.
Implications:
- This case highlights a rare but significant gastrointestinal complication in Menkes' disease.
- Advanced endoscopic techniques can effectively manage such bleeding polyps in infants.
- Further research into GI manifestations of MD is warranted.
Abstract:
We report a case of an infant with Menkes' disease (MD) presented at the age of five months, with coffee ground vomiting, melaena with a significant drop of haemoglobin. Urgent endoscopic assessment revealed a friable bleeding trans-pyloric multi-lobulated sessile polyp. Due to further significant upper gastrointestinal bleeding, polypectomy occurred. Endoscopic mucosal resection was performed with a grasp-and-snare technique using a dual channel operating gastroscope. Haemostasis was achieved by application of argon plasma coagulation where required. No perforation occurred. Repeated debridement was required 6 wk after which the growth was excised completely with no further blood transfusion required after that procedure. Histological examination confirmed ulcerated and inflamed hyperplastic polyp. We discuss our endoscopic technique and discuss the reported gastrointestinal manifestation of MD in the literature.
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