Suppr超能文献

小儿肠淋巴组织增生性肠套叠术后复发的外科治疗:肠切除是否总是必要?一例报告。

Surgical treatment of recurrent intussusception induced by intestinal lymphoid hyperplasia in a child: is bowel resection always necessary? A case report.

机构信息

Department of Dermatology, Weifang People's Hospital, Weifang, 261041, China.

Department of Endocrinology, Weifang People's Hospital, Weifang, 261041, China.

出版信息

BMC Surg. 2022 May 10;22(1):169. doi: 10.1186/s12893-022-01608-w.

Abstract

BACKGROUND

Intussusception recurrence (IR) induced by intestinal lymphoid hyperplasia (ILH) in children is rare, and surgical treatment is the final resort if IR is refractory to medications and non-surgical interventions. To date, only a few case reports have described surgical management of ILH-induced IR in children, all involving bowel resection regardless of whether there are bowel necrosis and perforation.

CASE PRESENTATION

A 2-year-old boy was transferred to our department due to IR. His main complaint was abdominal pain. Color Doppler ultrasound confirmed ileocecal intussusception while no other abnormalities were found. A final diagnosis of IR with unknown causes was made. Repeated saline enema reductions and dexamethasone failed to cure the IR. Laparotomy was eventually performed after almost 10 episodes of IR. Intraoperatively, distal ileum thickening with palpable masses without bowel necrosis and perforation was noted. ILH was suspected and a biopsy of the affected intestine was performed. Histopathological analysis confirmed ILH. The intussusception was manually reduced, the terminal ileum and the ileocecal junction were fixed to the paralleled ascending colon and the posterior peritoneum respectively, and no bowel resection was performed. The postoperative recovery was uneventful and no IR was observed during over 5 years of follow-up.

CONCLUSIONS

As far as we are aware, this is the first report of successful surgical treatment of ILH-induced pediatric IR without bowel resection in a child. Our experience suggests bowel resection may be unnecessary if bowel necrosis and perforation are absent.

摘要

背景

儿童肠淋巴组织增生(ILH)引起的肠套叠复发(IR)较为罕见,如果药物和非手术干预对 IR 无效,则手术治疗是最后的手段。迄今为止,只有少数病例报告描述了儿童 ILH 引起的 IR 的手术治疗,所有这些病例都涉及肠切除,无论是否存在肠坏死和穿孔。

病例介绍

一名 2 岁男孩因 IR 被转至我科。他的主要症状是腹痛。彩色多普勒超声证实回盲部肠套叠,无其他异常。最终诊断为原因不明的 IR。反复生理盐水灌肠复位和地塞米松治疗未能治愈 IR。在近 10 次 IR 发作后,最终进行了剖腹手术。术中发现回肠末端增厚,可触及肿块,但无肠坏死和穿孔。怀疑为 ILH,对受累肠段进行活检。组织病理学分析证实为 ILH。手动复位套叠,将末端回肠和回盲部固定于并行的升结肠和后腹膜,未行肠切除。术后恢复顺利,随访 5 年以上未见 IR。

结论

据我们所知,这是首例在儿童中成功手术治疗无肠切除的 ILH 引起的小儿 IR 的报告。我们的经验表明,如果不存在肠坏死和穿孔,肠切除可能是不必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aee/9092808/21e32b830e84/12893_2022_1608_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验