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婴儿期由 Peutz-Jeghers 错构瘤性息肉引起的回肠-回肠型肠套叠。

Ileo-ileal intussusception secondary to a Peutz-Jeghers hamartomatous polyp in an infant.

机构信息

Department of Paediatric Surgery, Royal Alexandra Children's Hospital, Brighton, UK

Department of Paediatric Surgery, Royal Alexandra Children's Hospital, Brighton, UK.

出版信息

BMJ Case Rep. 2024 Jul 25;17(7):e261464. doi: 10.1136/bcr-2024-261464.

Abstract

We report the case of ileo-ileal intussusception secondary to a Peutz-Jeghers syndrome (PJS) hamartomatous polyp in a male infant. The patient presented with non-bilious vomiting and a single episode of passing blood in his stool. An upper gastrointestinal contrast study showed proximal bowel obstruction. At laparotomy, ileo-ileal intussusception was identified with a papillary mass acting as a lead point. The mass was resected, and a primary anastomosis was performed. The patient recovered well and was discharged on postoperative day 5. Histological assessment diagnosed a PJS hamartoma. The patient was well at 1 month follow-up. This case report describes a rare cause of intussusception in an infant that should be considered in the differential diagnosis. The diagnosis of PJS in infancy is uncommon and requires long-term follow-up.

摘要

我们报告了一例男性婴儿因 Peutz-Jeghers 综合征(PJS)错构瘤性息肉引起的回肠-回肠套叠。该患者表现为非胆汁性呕吐和单次便血。上消化道造影检查显示近端肠阻塞。剖腹探查时发现回肠-回肠套叠,伴有作为牵引点的乳头状肿块。肿块被切除,并进行了一期吻合。患者恢复良好,术后第 5 天出院。组织学评估诊断为 PJS 错构瘤。患者在 1 个月随访时情况良好。本病例报告描述了一种婴儿肠套叠的罕见病因,在鉴别诊断中应考虑这一病因。婴儿期 PJS 的诊断并不常见,需要长期随访。

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Peutz-Jeghers syndrome. A case report.佩-吉二氏综合征。病例报告。
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