Peutz-Jeghers syndrome in women with jejunojejunal intussusception and multiple gastrointestinal polyposis: A case report.

IF 0.6 Q4 SURGERY International Journal of Surgery Case Reports Pub Date : 2025-01-01 Epub Date: 2024-12-01 DOI:10.1016/j.ijscr.2024.110713
Samrat Shrestha, Bijay Raj Bhatta, Mecklina Shrestha, Kaushal S Thapa
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Abstract

Introduction and importance: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by multiple gastrointestinal hamartomatous polyposis, mucocutaneous pigmentation, and/or a family history of PJS. Intussusception in patient with PJS is a common complication presenting as abdominal pain and a feature of intestinal obstruction secondary to polyps.

Case presentation: A 36-year-old woman presented to the emergency department with bilateral flank pain, melena, and generalized fatigue with multiple, black-pigmented lesions on her lips extending to mucosa of buccal cavity. Contrast-enhanced computed tomography confirmed multiple gastrointestinal polyps with jejuno-jejunal intussusception. Exploratory laparotomy revealed jejuno-jejunal intussusception with multiple pedunculated polyps. Segmental jejunal resection followed by jejunojejunal stapled anastomosis was performed. Histopathological examination revealed a hamartomatous polyp, confirming the diagnosis of PJS.

Clinical discussion: PJS is a rare autosomal disorder due to a mutation in the tumor suppressor gene STK11, found on chromosome 19p13. The estimated prevalence of PJS ranges between 1 in 8300 and 1 in 280,000. Intussusception is one of the most common complications, occurring in almost half the patients. Surgical resection remains the recommended treatment for rapidly growing polyps associated with intussusception. Screening at regular intervals for early detection of cancers and recurrence of polyps after excision is recommended.

Conclusion: Accurate diagnosis of PJS depends on childhood history, family history, physical examination, endoscopic evaluation, and genetic testing. Their presentation varies, ranging from gastointestinal bleeding to intestinal obstruction brought on by intussusception. Surgical resections remain the recommended treatment in patients with intussusception associated with large and rapidly growing polyps.

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Peutz-Jeghers综合征并发空肠肠套叠和多发性胃肠道息肉病1例报告。
简介及重要性:Peutz-Jeghers综合征(PJS)是一种罕见的常染色体显性遗传病,其特征为多发性胃肠道错构瘤性息肉病、粘膜皮肤色素沉着和/或PJS家族史。肠套叠是PJS患者常见的并发症,表现为腹痛和继发于息肉的肠梗阻。病例介绍:一名36岁女性,因双侧侧腹疼痛、黑黑和全身疲劳,并伴有唇部多发黑色色素病变,并延伸至口腔黏膜就诊。增强计算机断层扫描证实多发性胃肠道息肉伴空肠-空肠肠套叠。剖腹探查发现空肠-空肠肠套叠伴多发带蒂息肉。采用节段性空肠切除后空肠吻合术。组织病理学检查显示一个错构瘤息肉,确认PJS的诊断。临床讨论:PJS是一种罕见的常染色体疾病,由于肿瘤抑制基因STK11突变,发现在染色体19p13。PJS的患病率估计在1 / 8300到1 / 280,000之间。肠套叠是最常见的并发症之一,几乎有一半的患者发生。手术切除仍然是快速生长的息肉与肠套叠的推荐治疗方法。建议定期进行筛查,以便及早发现癌症和息肉切除后的复发。结论:PJS的准确诊断依赖于儿童史、家族史、体格检查、内窥镜检查和基因检测。它们的表现各不相同,从胃肠道出血到肠套叠引起的肠梗阻。手术切除仍然是肠套叠合并大而快速生长的息肉患者的推荐治疗方法。
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CiteScore
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1116
审稿时长
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