Polyp Clearance via Operative and Endoscopic Polypectomy in Patients With Peutz-Jeghers Syndrome After Multiple Small Bowel Resections
Do-Hyun LEE; Hyun-Deok SHIN; Woo-Hee CHO; Kyoung-Hwang SHIN; Sora LEE; Jeong-Eun SHIN; Hwan NAMGUNG; Ji-Eun GWON.
Intestinal Research
; : 320-327, 2014.
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| WPRIM | ID: wpr-50695
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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