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患有空肠空肠套叠和多发性胃肠道息肉的女性的黑斑息肉综合征:一例报告。

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

作者信息

Shrestha Samrat, Bhatta Bijay Raj, Shrestha Mecklina, Thapa Kaushal S

机构信息

National Academy of Medical Sciences, NAMS, Bir Hospital, Department of General Surgery, Kathmandu, Nepal.

National Academy of Medical Sciences, NAMS, Bir Hospital, Department of General Surgery, Kathmandu, Nepal.

出版信息

Int J Surg Case Rep. 2025 Jan;126:110713. doi: 10.1016/j.ijscr.2024.110713. Epub 2024 Dec 1.

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.

摘要

引言与重要性

黑斑息肉综合征(PJS)是一种罕见的常染色体显性疾病,其特征为多发胃肠道错构瘤性息肉、黏膜皮肤色素沉着和/或有PJS家族史。PJS患者发生肠套叠是一种常见并发症,表现为腹痛,是息肉继发肠梗阻的一个特征。

病例介绍

一名36岁女性因双侧胁腹疼痛、黑便和全身乏力就诊于急诊科,其嘴唇有多个黑色色素沉着病变,延伸至颊腔黏膜。增强计算机断层扫描证实有多发胃肠道息肉伴空肠-空肠套叠。剖腹探查发现空肠-空肠套叠伴多个带蒂息肉。行节段性空肠切除,随后进行空肠-空肠吻合器吻合术。组织病理学检查显示为错构瘤性息肉,确诊为PJS。

临床讨论

PJS是一种罕见的常染色体疾病,由位于19p13染色体上的肿瘤抑制基因STK11突变引起。PJS的估计患病率在8300分之一至280000分之一之间。肠套叠是最常见的并发症之一,几乎半数患者会发生。手术切除仍然是与肠套叠相关的快速生长息肉的推荐治疗方法。建议定期筛查,以便早期发现癌症和息肉切除后复发情况。

结论

PJS的准确诊断取决于儿童期病史、家族史、体格检查、内镜评估和基因检测。其表现各异,从胃肠道出血到肠套叠引起的肠梗阻。对于伴有大的快速生长息肉的肠套叠患者,手术切除仍然是推荐的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e103/11650254/7619517efde0/gr1.jpg

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