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Polyp Clearance via Operative and Endoscopic Polypectomy in Patients With Peutz-Jeghers Syndrome After Multiple Small
Do Hyun Lee1, Hyun Deok Shin1, Woo Hee Cho1
1Department of Internal Medicine, Dankook University Hospital, Dankook University College of Medicine, Cheonan, Korea.
Insights
Peutz-Jeghers syndrome patients can benefit from combined operative and endoscopic polypectomy. This approach effectively removes numerous polyps, reducing complications from repeated surgeries.
Area of Science:
- Gastroenterology
- Genetics
- Surgical Oncology
Background:
- Peutz-Jeghers syndrome (PJS) is an inherited disorder characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyps.
- PJS polyps frequently lead to complications such as intussusception and intestinal hemorrhage, necessitating frequent surgical interventions.
- Patients with PJS often undergo multiple laparotomies and intestinal resections throughout their lives.
Purpose of the Study:
- To report a case of Peutz-Jeghers syndrome managed with a combined operative and endoscopic polypectomy technique.
- To evaluate the efficacy of this combined approach in managing extensive polyposis in a PJS patient.
- To highlight the benefits of this technique in reducing the need for frequent laparotomies and associated complications.
Main Methods:
- A 40-year-old male patient with a 20-year history of Peutz-Jeghers syndrome and prior intestinal resections was treated.
- A combined operative and endoscopic polypectomy strategy was employed to remove gastrointestinal polyps.
- Over 100 polyps were successfully removed using this integrated approach.
Main Results:
- The combined operative and endoscopic polypectomy successfully removed more than 100 hamartomatous polyps.
- This technique resulted in a "clean" small intestine, significantly reducing the polyp burden.
- The intervention aimed to provide a longer interval between future surgical procedures.
Conclusions:
- Combined operative and endoscopic polypectomy is an effective strategy for managing extensive polyposis in Peutz-Jeghers syndrome.
- This approach can significantly reduce the frequency of major abdominal surgeries and their associated morbidity.
- The technique offers a promising method for improving long-term patient outcomes in Peutz-Jeghers syndrome.
Abstract:
Peutz-Jeghers syndrome is an autosomal dominant inherited disease that manifests as a combination of mucocutaneous pigmentation and gastrointestinal hamartomatous polyps that usually cause intussusception and intestinal hemorrhage. We report the case of a 40-year-old male patient who was diagnosed 20 years ago and had previously undergone 3 intestinal resection surgeries. This time, with the use of combined operative and endoscopic polypectomy, more than 100 polyps were removed. This technique is useful for providing a "clean" small intestine that allows the patient a long interval between laparotomies and reduces the complications associated with multiple laparotomies and resections.
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