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本文引用的文献

1
Dural arteriovenous malformation in a child with Bannayan-Riley-Ruvalcaba Syndrome.患有班纳扬-莱利-鲁瓦尔卡瓦综合征的儿童的硬脑膜动静脉畸形。
AJNR Am J Neuroradiol. 2006 Oct;27(9):1927-9.
2
Cerebral venous malformations have distinct genetic origin from cerebral cavernous malformations.脑静脉畸形与脑海绵状畸形有着不同的遗传起源。
Stroke. 2005 Nov;36(11):2479-80. doi: 10.1161/01.STR.0000183616.99139.d3. Epub 2005 Oct 20.
3
The PTEN/PI3K pathway governs normal vascular development and tumor angiogenesis.PTEN/PI3K信号通路调控正常血管发育和肿瘤血管生成。
Genes Dev. 2005 Sep 1;19(17):2054-65. doi: 10.1101/gad.1308805. Epub 2005 Aug 17.
4
Arteriovenous malformations in Cowden syndrome.考登综合征中的动静脉畸形
J Med Genet. 2005 Aug;42(8):e50. doi: 10.1136/jmg.2004.030569.
5
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.患有自闭症谱系障碍且伴有极端巨头畸形的个体亚组,与生殖系PTEN肿瘤抑制基因突变有关。
J Med Genet. 2005 Apr;42(4):318-21. doi: 10.1136/jmg.2004.024646.
6
Brain magnetic resonance imaging in patients with Cowden syndrome.考登综合征患者的脑部磁共振成像
Medicine (Baltimore). 2005 Mar;84(2):129-136. doi: 10.1097/01.md.0000158792.24888.d2.
7
The biology and clinical relevance of the PTEN tumor suppressor pathway.PTEN肿瘤抑制通路的生物学特性及临床相关性。
J Clin Oncol. 2004 Jul 15;22(14):2954-63. doi: 10.1200/JCO.2004.02.141.
8
Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome.真正的考登综合征(再次)请站出来好吗?PTEN错构瘤肿瘤综合征的突变谱和临床谱的扩展
J Med Genet. 2004 May;41(5):323-6. doi: 10.1136/jmg.2004.018036.
9
Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.班纳扬-莱利-鲁瓦尔卡瓦综合征:PTEN 突变阳性病例的表型进一步描述及管理
Fam Cancer. 2003;2(2):79-85. doi: 10.1023/a:1025713815924.
10
Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.考登/班纳扬-莱利-鲁瓦尔卡巴综合征中的种系PTEN启动子突变和缺失导致PTEN蛋白异常以及磷酸肌醇-3-激酶/蛋白激酶B信号通路失调。
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携带PTEN突变患者的血管异常谱系:对诊断和管理的意义。

The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.

作者信息

Tan Wen-Hann, Baris Hagit N, Burrows Patricia E, Robson Caroline D, Alomari Ahmad I, Mulliken John B, Fishman Steven J, Irons Mira B

出版信息

J Med Genet. 2007 Sep;44(9):594-602. doi: 10.1136/jmg.2007.048934. Epub 2007 May 25.

DOI:10.1136/jmg.2007.048934
PMID:17526801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2597949/
Abstract

BACKGROUND

Mutations in the PTEN gene cause two disorders that predispose to cancer, Bannayan-Riley-Ruvalcaba and Cowden syndromes. Some patients with a PTEN mutation have only macrocephaly and autism, but they may still be at risk for neoplasms. Vascular anomalies occur in patients with a PTEN mutation, but they have not been systematically studied or precisely defined.

METHOD

We analysed the clinical and radiological features of the vascular anomalies in 26 patients with PTEN mutations who were either seen or had their medical records reviewed at Children's Hospital Boston.

RESULTS

All 23 patients who had their head circumference measured were macrocephalic, and all 13 male patients who were fully examined had penile freckling. Vascular anomalies were found in 14/26 (54%) of patients: 8/14 (57%) had multiple lesions and 11/13 (85%) who had cross-sectional imaging had intramuscular vascular lesions. Radiographic studies showed that 12/14 (86%) were fast-flow vascular anomalies, and angiography typically showed focal segmental dilatation of draining veins. Excessive ectopic fat in the vascular anomalies was present in 11/12 (92%) of patients on CT or MRI. Intracranial developmental venous anomalies (DVAs) were found in 8/9 (89%) of patients who had brain MRI with contrast.

CONCLUSIONS

Vascular anomalies in patients with a PTEN mutation are typically multifocal intramuscular combinations of fast-flow channels and ectopic fat. Cerebral DVAs are very common. PTEN mutational analysis should be considered for all macrocephalic patients with fast-flow vascular anomalies or multiple intracranial DVAs.

摘要

背景

PTEN基因突变会引发两种易患癌症的疾病,即巴纳扬-莱利-鲁瓦尔卡瓦综合征和考登综合征。一些携带PTEN基因突变的患者仅表现为巨头症和自闭症,但他们仍可能有患肿瘤的风险。PTEN基因突变的患者会出现血管异常,但尚未对其进行系统研究或精确界定。

方法

我们分析了26例携带PTEN基因突变患者的血管异常的临床和放射学特征,这些患者均在波士顿儿童医院就诊或其病历被回顾。

结果

所有23例测量头围的患者均为巨头症,所有13例接受全面检查的男性患者均有阴茎雀斑。14/26(54%)的患者发现有血管异常:8/14(57%)有多处病变,13例接受横断面成像检查的患者中有11/13(85%)有肌肉内血管病变。影像学研究显示,12/14(86%)为高流量血管异常,血管造影通常显示引流静脉的局灶性节段性扩张。11/12(92%)的患者在CT或MRI上显示血管异常中有过多的异位脂肪。在9例接受增强脑MRI检查的患者中,8/9(89%)发现有颅内发育性静脉异常(DVA)。

结论

携带PTEN基因突变患者的血管异常通常是高流量通道和异位脂肪的多灶性肌肉内组合。脑DVA非常常见。对于所有患有高流量血管异常或多处颅内DVA的巨头症患者,均应考虑进行PTEN突变分析。