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4岁女童蓝色橡皮疱痣综合征的内镜治疗及长期随访:病例报告

Endoscopic treatment of blue rubber bleb nevus syndrome in a 4-year-old girl with long-term follow-up: A case report.

作者信息

Marakhouski Kirill, Sharafanovich Elena, Kolbik Uladzislau, Sautin Aleh, Nikalayeva Katsiaryna, Pataleta Aleh, Sanfirau Kiryl, Svirsky Aliaksandr

机构信息

Diagnostic Division, Republican Scientific and Practical Center of Pediatric Surgery, Minsk 220113, Belarus.

Department of Elective Surgery, Republican Scientific and Practical Center of Pediatric Surgery, Minsk 220113, Belarus.

出版信息

World J Gastrointest Endosc. 2021 Mar 16;13(3):90-96. doi: 10.4253/wjge.v13.i3.90.

Abstract

BACKGROUND

Blue rubber bleb nevus syndrome (BRBNS) is a rare vascular disease, difficult to diagnose and choose a treatment method, especially in young children. There are several limiting factors to the use of enteroscopy for diagnostics and treatment in pediatric patients, in general. The literature on BRBNS cases is limited and presents various therapeutic approaches.

CASE SUMMARY

We present here a case of BRBNS involving a 4-year-old female, whose intestinal venous lesions were successfully treated by endoscopic sclerotherapy and aethoxysklerol foam. Skin lesions, typical for BRBNS, appeared on the 8 d of the child's life and their number increased over the next several months. The child also experienced episodes of critical decrease in hemoglobin level (by as much as 52 g/L) for several years, requiring iron supplementation and several blood transfusions. Video capsule endoscopy revealed numerous vascular formations in the small bowel. The combined findings of gastrointestinal venous formations and skin lesions prompted BRBNS diagnosis. Single-balloon enteroscopy was used to perform sclerotherapy, with aethoxysklerol foam. A positive effect was observed within 19 mo of follow-up. We continue to monitor the patient's hemoglobin level, every 2 wk, and it has remained satisfactory (> 120 g/L).

CONCLUSION

Endoscopic sclerotherapy can be effective in the clinical management of gastrointestinal manifestations of BRBNS in young children.

摘要

背景

蓝色橡皮疱痣综合征(BRBNS)是一种罕见的血管疾病,诊断和选择治疗方法都很困难,尤其是在幼儿中。一般来说,小儿患者使用小肠镜进行诊断和治疗存在几个限制因素。关于BRBNS病例的文献有限,且呈现出各种治疗方法。

病例摘要

我们在此报告一例4岁女性BRBNS病例,其肠道静脉病变通过内镜下硬化治疗和聚多卡醇泡沫成功治愈。BRBNS典型的皮肤病变在患儿出生后第8天出现,在接下来的几个月里数量增加。该患儿还在数年中经历了血红蛋白水平严重下降(多达52 g/L)的情况,需要补充铁剂并多次输血。视频胶囊内镜检查发现小肠内有大量血管畸形。胃肠道静脉畸形和皮肤病变的综合表现提示BRBNS诊断。使用单气囊小肠镜进行硬化治疗,采用聚多卡醇泡沫。随访19个月内观察到了积极效果。我们继续每2周监测患者的血红蛋白水平,其一直保持令人满意(>120 g/L)。

结论

内镜下硬化治疗对幼儿BRBNS的胃肠道表现进行临床管理可能有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98d9/7958468/4640652e4056/WJGE-13-90-g001.jpg

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