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儿童蓝色橡皮疱痣综合征的诊断和治疗:多中心病例系列。

Diagnosis and management of children with Blue Rubber Bleb Nevus Syndrome: A multi-center case series.

机构信息

Centre of Paediatric Gastroenterology, Sheffield Children's Hospital, Sheffield, United Kingdom.

Centre of Paediatric Gastroenterology, Sheffield Children's Hospital, Sheffield, United Kingdom.

出版信息

Dig Liver Dis. 2019 Nov;51(11):1537-1546. doi: 10.1016/j.dld.2019.04.020. Epub 2019 Jul 26.

Abstract

BACKGROUND

Blue Rubber Bleb Nevus Syndrome (BRBNS) is a rare, severe, sporadically occurring disorder characterized by multiple venous malformations.

AIMS

To present and analyze a case series of pediatric patients with BRBNS and to describe diagnostic approaches and management options applied.

PATIENTS AND METHODS

Multicenter, retrospective study, evaluating the diagnosis and management of children with BRBNS.

RESULTS

Eighteen patients diagnosed with BRBNS were included. Cutaneous venous malformations were observed in 78% and gastrointestinal venous malformations in 89%. Lesions were also found in other organs including muscles, joints, central nervous system, eyes, parotid gland, spine, kidneys and lungs. Gastrointestinal lesions were more common in the small intestine than in stomach or colon. The management varied significantly among centers. Endoscopic therapy and surgical therapy alone failed to prevent recurrence of lesions. In younger children and in patients with musculoskeletal or other organ involvement, sirolimus was used with 100% success rate in our series (5 patients treated) although poor compliance with subtherapeutic sirolimus trough levels led to recurrence in a minority.

CONCLUSIONS

Considering the multi-organ involvement in BRBNS, diagnosis and management requires a multidisciplinary approach. The treatment includes conservative, medical, endoscopic and surgical options. Prospective multicenter studies are needed to identify the optimal management of this rare condition.

摘要

背景

蓝色橡皮疱痣样静脉畸形综合征(BRBNS)是一种罕见的、严重的、偶发性疾病,其特征为多发性静脉畸形。

目的

介绍并分析一组 BRBNS 儿科患者的病例系列,并描述所应用的诊断方法和治疗选择。

患者与方法

多中心回顾性研究,评估 BRBNS 患儿的诊断和治疗。

结果

共纳入 18 例诊断为 BRBNS 的患者。78%的患者存在皮肤静脉畸形,89%的患者存在胃肠道静脉畸形。病变还见于其他器官,包括肌肉、关节、中枢神经系统、眼睛、腮腺、脊柱、肾脏和肺部。胃肠道病变在小肠比在胃或结肠更常见。各中心的治疗方法差异很大。单独的内镜治疗和手术治疗均未能预防病变复发。在年龄较小的儿童和存在肌肉骨骼或其他器官受累的患者中,我们的研究中使用西罗莫司治疗,成功率为 100%(5 例患者接受治疗),尽管少数患者因西罗莫司谷浓度低于治疗水平而导致复发。

结论

鉴于 BRBNS 的多器官受累,诊断和治疗需要多学科方法。治疗包括保守治疗、药物治疗、内镜治疗和手术治疗。需要开展前瞻性多中心研究,以确定这种罕见疾病的最佳治疗方法。

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