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儿童蓝色橡皮疱痣综合征的诊断与治疗

Diagnosis and treatment of blue rubber bleb nevus syndrome in children.

作者信息

Deng Zhao-Hui, Xu Chun-Di, Chen Shun-Nian

机构信息

Institute of the Shanghai Children's Medical Center, Jiao Tong University, Shanghai 200127, China.

出版信息

World J Pediatr. 2008 Feb;4(1):70-3. doi: 10.1007/s12519-008-0015-9.

Abstract

BACKGROUND

Blue rubber bleb nevus syndrome (BRBNS) is characterized by distinctive vascular malformations of skin and the gastrointestinal tract, often leading to chronic anemia and intestinal bleeding. It usually presents right after birth or during early infancy. Though the disease is inherent, its occurrence is sporadic. Thus it is usually not timely diagnosed. We analyzed the clinical characteristics and treatment of this disorder in order to improve the diagnosis and treatment.

METHODS

Three patients with BRBNS treated at our hospital during 2002-2003 and 39 patients from the literature reported during 1965-2003 were reviewed in terms of the diagnosis and treatment. BRBNS may be diagnosed as cutaneous cavernous hemangioma associated with the same lesion of the gastrointestinal tract and other organs.

RESULTS

Our 3 patients suffered from cutaneous angioma and gastrointestinal hemangioma. In 39 patients reported in the literature, cutaneous angioma was observed in all of them, and gastrointestinal hemangioma in 31. Additionally, the lesions were also found in other organs such as the brain (7 patients), joint (2), liver (2), eye (1), kidney (1) and spleen (1). Cutaneous angioma was located on the surface of the skin, including body (93%), limbs (86%), hip (36%) and face (26%). Gastrointestinal hemangioma was more common in the small intestine (100%) than in the colon (74%) and stomach (26%). When the joint was involved by hemangioma, pathologic fracture or overgrowth of bone needed traction and amputation (1 patient respectively). For significant gastrointestinal bleeding, endoscopic techniques (8 patients), surgical excision (5), or both (1) were performed. Recurrent bleeding was successfully treated by endoscopic laser combined with steroid or interferon in one patient.

CONCLUSIONS

BRBNS in children presents atypical symptom and systemic complications. It should be dealt with seriously if gastrointestinal bleeding or orthopedic complication occurs. Treatment includes conservative, endoscopic and surgical options. Its recurrence with new angioma in the gastrointestinal tract needs laser-steroid therapy.

摘要

背景

蓝色橡皮疱痣综合征(BRBNS)的特征是皮肤和胃肠道出现独特的血管畸形,常导致慢性贫血和肠道出血。它通常在出生后或婴儿早期出现。尽管该疾病是先天性的,但其发生是散发性的。因此,通常不能及时诊断。我们分析了这种疾病的临床特征和治疗方法,以改善诊断和治疗。

方法

回顾了2002年至2003年在我院接受治疗的3例BRBNS患者以及1965年至2003年文献报道的39例患者的诊断和治疗情况。BRBNS可被诊断为与胃肠道及其他器官相同病变相关的皮肤海绵状血管瘤。

结果

我们的3例患者患有皮肤血管瘤和胃肠道血管瘤。在文献报道的39例患者中,均观察到皮肤血管瘤,31例有胃肠道血管瘤。此外,在其他器官如脑(7例)、关节(2例)、肝脏(2例)、眼(1例)、肾脏(1例)和脾脏(1例)也发现了病变。皮肤血管瘤位于皮肤表面,包括躯干(93%)、四肢(86%)、臀部(36%)和面部(26%)。胃肠道血管瘤在小肠(100%)比在结肠(74%)和胃(26%)更常见。当关节被血管瘤累及,病理性骨折或骨过度生长分别需要牵引和截肢(各1例患者)。对于严重的胃肠道出血,采用了内镜技术(8例患者)、手术切除(5例)或两者结合(1例)。1例复发性出血患者通过内镜激光联合类固醇或干扰素成功治疗。

结论

儿童BRBNS表现出非典型症状和全身并发症。如果发生胃肠道出血或骨科并发症,应予以重视。治疗包括保守、内镜和手术选择。其胃肠道新血管瘤复发需要激光-类固醇治疗。

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