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本文引用的文献

1
A retrospective analysis of low dose, intranasal injected bevacizumab (Avastin) in hereditary haemorrhagic telangiectasia.遗传性出血性毛细血管扩张症患者低剂量经鼻内注射贝伐单抗(阿瓦斯汀)的回顾性分析。
Eur Arch Otorhinolaryngol. 2012 Feb;269(2):531-6. doi: 10.1007/s00405-011-1721-9. Epub 2011 Jul 31.
2
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.遗传性出血性毛细血管扩张症:病理生理学、诊断与治疗。
Blood Rev. 2010 Nov;24(6):203-19. doi: 10.1016/j.blre.2010.07.001. Epub 2010 Sep 25.
3
Dextran sulfate sodium leads to chronic colitis and pathological angiogenesis in Endoglin heterozygous mice.硫酸葡聚糖钠诱导内皮糖蛋白杂合子小鼠发生慢性结肠炎和病理性血管生成。
Inflamm Bowel Dis. 2010 Nov;16(11):1859-70. doi: 10.1002/ibd.21288.
4
Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia.遗传性出血性毛细血管扩张症小鼠模型中新生动静脉畸形的实时成像
J Clin Invest. 2009 Nov;119(11):3487-96. doi: 10.1172/JCI39482. Epub 2009 Oct 1.
5
Hereditary haemorrhagic telangiectasia: a clinical and scientific review.遗传性出血性毛细血管扩张症:临床与科学综述
Eur J Hum Genet. 2009 Jul;17(7):860-71. doi: 10.1038/ejhg.2009.35. Epub 2009 Apr 1.
6
Liver involvement in hereditary hemorrhagic telangiectasia (HHT).遗传性出血性毛细血管扩张症(HHT)中的肝脏受累情况。
J Hepatol. 2007 Mar;46(3):499-507. doi: 10.1016/j.jhep.2006.12.008. Epub 2007 Jan 2.
7
A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7.遗传性出血性毛细血管扩张症的第四个基因座定位于7号染色体。
Am J Med Genet A. 2006 Oct 15;140(20):2155-62. doi: 10.1002/ajmg.a.31450.
8
Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.在对200名接受遗传性出血性毛细血管扩张症(HHT)临床基因检测的个体进行的研究中,发现ENG和ACVRL1基因的新突变:基因型与表型的相关性。
Hum Mutat. 2006 Jul;27(7):667-75. doi: 10.1002/humu.20342.
9
Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients.法国遗传性出血性毛细血管扩张症(HHT)患者中ENG和ACVRL1(ALK1)突变的分布情况。
Hum Mutat. 2006 Jun;27(6):598. doi: 10.1002/humu.9421.
10
Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures.遗传性出血性毛细血管扩张症:临床表现与诊断方法的最新进展
Wien Klin Wochenschr. 2006 Mar;118(3-4):72-80. doi: 10.1007/s00508-006-0561-x.

遗传性出血性毛细血管扩张症 2 型患者的胃血管发育不良。

Gastric angiodysplasia in a hereditary hemorrhagic telangiectasia type 2 patient.

机构信息

Department of Gastroenterology, Gachon University Gil Medical Center, Incheon 402-751, South Korea.

出版信息

World J Gastroenterol. 2012 Apr 21;18(15):1840-4. doi: 10.3748/wjg.v18.i15.1840.

DOI:10.3748/wjg.v18.i15.1840
PMID:22553411
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3332300/
Abstract

Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people. Clinical diagnosis of HHT is made when a person presents three of the following four criteria: family history, recurrent nosebleeds, mucocutaneous telangiectasis, and arteriovenous malformations (AVM) in the brain, lung, liver and gastrointestinal (GI) tract. Although epistaxis is the most common presenting symptom, AVMs affecting the lungs, brain and GI tract provoke a more serious outcome. Heterozygous mutations in endoglin, activin receptor-like kinase 1 (ACVRL1; ALK1), and SMAD4, the genes involved in the transforming growth factor-β family signaling cascade, cause HHT. We report here the case of a 63 year-old male patient who presented melena and GI bleeding episodes, proven to be caused by bleeding from multiple gastric angiodysplasia. Esophagogastroduodenoscopy revealed multiple angiodysplasia throughout the stomach. Endoscopic argon plasma coagulation was performed to control bleeding from a gastric angiodysplasia. The patient has been admitted several times with episodes of hemoptysis and hematochezia. One year ago, the patient was hospitalized due to right-sided weakness, which was caused by left basal ganglia hemorrhage as the part of HHT presentation. In family history, the patient's mother and elder sister had died, due to intracranial hemorrhage, and his eldest son has been suffered from recurrent epistaxis for 20 years. A genetic study revealed a mutation in exon 3 of ALK1 (c.199C > T; p.Arg67Trp) in the proband and his eldest son presenting epistaxis.

摘要

遗传性出血性毛细血管扩张症(HHT)是一种罕见的常染色体显性遗传性疾病,发病率约为每 5000 至 8000 人中 1 例。当一个人出现以下四个标准中的三个时,即可临床诊断为 HHT:家族史、反复发作的鼻出血、黏膜皮肤毛细血管扩张症和脑、肺、肝和胃肠道(GI)的动静脉畸形(AVM)。尽管鼻出血是最常见的首发症状,但影响肺部、大脑和胃肠道的 AVM 会导致更严重的后果。编码转化生长因子-β家族信号级联的内 Engl、激活素受体样激酶 1(ACVRL1;ALK1)和 SMAD4 基因的杂合突变导致 HHT。我们在此报告 1 例 63 岁男性患者,其表现为黑便和 GI 出血发作,经证实是由多发胃血管扩张症引起的出血。食管胃十二指肠镜检查显示整个胃内有多发性血管扩张症。进行内镜氩等离子凝固术以控制胃血管扩张症的出血。该患者因咯血和血便反复发作多次入院。一年前,该患者因右侧无力住院,这是 HHT 表现的一部分,由左侧基底节出血引起。家族史中,患者的母亲和姐姐因颅内出血死亡,他的大儿子因反复发作鼻出血已有 20 年。基因研究显示先证者和有鼻出血的大儿子的 ALK1 外显子 3 中存在突变(c.199C > T;p.Arg67Trp)。