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蓝色橡皮疱痣综合征:病例报告及文献复习

Blue rubber bleb nevus syndrome: case report and literature review.

作者信息

Dobru Daniela, Seuchea Nicolae, Dorin Marian, Careianu Valentin

机构信息

Gastroenterology Department, Emergency Hospital, Str. Gh. Marinescu no.1, Targu Mures, Romania.

出版信息

Rom J Gastroenterol. 2004 Sep;13(3):237-40.

Abstract

Blue Rubber Bleb Nevus Syndrome ( BRBNS) is a rare disorder characterized by multiple cutaneous venous malformations in the skin and gastrointestinal tract associated with intestinal hemorrhage and iron deficiency anemia. Other organs may also be involved. BRBNS has a potential for serious or fatal bleeding. The causes of this syndrome are unknown. Its most common presentation is in the form of sporadic cases, but dominant autosomal inheritance has been described. Although it was first recognized by Gascoyen in 1860, only one hundred years later did Bean further describe these lesions and coined the term BRBNS. A MEDLINE search yielded about 200 case reports published till 2003. We present a case of this syndrome diagnosed in a 16- year - old patient with both upper and lower gastrointestinal bleeding. He had severe anemia and venous swellings on the trunk. Similar lesions were found in the stomach, bowel and on his foot. In addition, we review the available literature on the epidemiology, clinical features, associated conditions, diagnosis and treatment.

摘要

蓝色橡皮疱痣综合征(BRBNS)是一种罕见的疾病,其特征为皮肤和胃肠道出现多发性皮肤静脉畸形,并伴有肠道出血和缺铁性贫血。其他器官也可能受累。BRBNS有发生严重或致命性出血的风险。该综合征的病因尚不清楚。其最常见的表现形式为散发病例,但也有常染色体显性遗传的报道。尽管1860年Gascoyen首次认识到该病,但直到100年后Bean才进一步描述了这些病变,并创造了“蓝色橡皮疱痣综合征”这一术语。截至2003年,通过医学文献数据库检索到约200例病例报告。我们报告一例16岁患有上、下消化道出血的该综合征患者。他患有严重贫血,躯干有静脉肿胀。在其胃部、肠道和足部发现了类似病变。此外,我们还综述了关于该综合征的流行病学、临床特征、相关疾病、诊断和治疗的现有文献。

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