A case of jejunal solitary Peutz–Jeghers polyp with intussusception identified by double-balloon enteroscopy

Solitary Peutz–Jeghers polyp is a rare hamartomatous polyp that has similar histologic characteristics with those of polyps in Peutz–Jeghers syndrome, without associated mucocutaneous hyperpigmentation and a family history. Previous reports indicated that solitary Peutz–Jeghers polyp is rarely found in the small intestine. We experienced a rare case of jejunal solitary Peutz–Jeghers polyp. A 29-year-old man was admitted to our hospital with a 6-month history of upper abdominal pain. He had no hyperpigmentation or a family history of Peutz–Jeghers syndrome. Abdominal computed tomography showed a 3-cm tumor-like structure at the tip of a mildly intussuscepted jejunum. Per oral double-balloon enteroscopy revealed a 3-cm pedunculated polyp in the jejunum. The patient underwent partial jejunal resection under laparotomy. Macroscopically, the surgical specimen showed a pedunculated polyp, measuring 30 × 15 × 10 mm in size, with lobulated head. Histopathologic examination revealed irregular aggregation of hyperplastic crypts with branching muscular bundles originating from the muscularis mucosae. Based on these histologic findings, we finally diagnosed the patient as a solitary Peutz–Jeghers polyp in the jejunum. The present case indicated that solitary Peutz–Jeghers polyp should be considered in a patient with solitary hamartomatous polyp in the gastrointestinal tract.