Suppr超能文献

儿童急腹症罕见盲肠病变病因。

Rare cecum pathologies as a cause of acute abdomen in children.

机构信息

Department of Pediatric Surgery, Mehmet Akif İnan Training and Research Hospital, Şanlıurfa-Turkey.

Department of Pediatric Surgery, ŞanlıurfaTraining and Research Hospital, Şanlıurfa-Turkey.

出版信息

Ulus Travma Acil Cerrahi Derg. 2022 Mar;28(3):249-253. doi: 10.14744/tjtes.2020.79357.

Abstract

BACKGROUND

We aimed to present cecum pathologies which are the cause of acute abdomen.

METHODS

Between January 2015 and June 2019, patients that were operated with the diagnosis of acute abdomen and patients with the primary cecum pathologies were evaluated retrospectively.

RESULTS

There were eight patients, five males and three females. The mean age was 7.2±2.9 years. Complaints were abdominal pain and vomiting in all patients. Physical examination was consistent with acute abdomen. In the imaging studies, the preliminary diagnosis was considered as two patients had acute appendicitis, two had invagination (one due to Meckel diverticulum and one with mesenteric cyst), two had ileus, one had perforated appendicitis, and one had cecum diverticulum. In surgery, five patients had cecum mass, one had cecum diverticulitis, one had cecum volvulus, and one had inflamed necrotic cecum. All patients underwent cecum resection and ileocolonic anastomosis. Histopathologic examination was resulted as Burkitt's lymphoma in three patients, cecum diverticulum in two, duplication of cecum in one, tuberculosis of cecum in one, and gangrenous necrosis due to volvulus in one patient. The mean follow-up period was 25 months (2 months-4 years). Follow-up was uneventful.

CONCLUSION

Primary cecum pathologies are very rare. This leads to lack of standardization in treatment planning. Considering the patients with malignancy in the series, ileocolonic anastomosis with cecum resection is an adequate and appropriate treatment option in children with primary cecum pathology.

摘要

背景

本研究旨在阐述导致急腹症的盲肠病变。

方法

回顾性分析 2015 年 1 月至 2019 年 6 月期间以急腹症行手术治疗且原发病灶位于盲肠的患者。

结果

共有 8 例患者,男 5 例,女 3 例,平均年龄 7.2±2.9 岁。所有患者均表现为腹痛、呕吐。体格检查均符合急腹症表现。影像学检查初步诊断为急性阑尾炎 2 例,肠套叠 2 例(1 例由 Meckel 憩室引起,1 例伴肠系膜囊肿),肠梗阻 2 例,穿孔性阑尾炎 1 例,盲肠憩室 1 例。手术中,5 例患者发现盲肠肿块,1 例盲肠憩室炎,1 例盲肠扭转,1 例盲肠炎症伴坏死。所有患者均接受了盲肠切除术和回结肠吻合术。病理检查结果为 Burkitt 淋巴瘤 3 例,盲肠憩室 2 例,盲肠重复畸形 1 例,盲肠结核 1 例,盲肠扭转导致的坏疽性坏死 1 例。平均随访时间为 25 个月(2 个月-4 年)。随访期间无不良事件发生。

结论

盲肠原发性疾病非常罕见,导致治疗方案缺乏标准化。考虑到本研究系列中存在恶性肿瘤患者,对于盲肠原发性疾病患儿,盲肠切除加回肠结肠吻合术是一种充分且合适的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccbf/10493532/ea217e389a99/TJTES-28-249-g001.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