Literature DB >> 23125071

Arteriovenous malformations and other vascular malformation syndromes.

Kevin J Whitehead1, Matthew C P Smith, Dean Y Li.   

Abstract

Vascular malformations are a disruption of the normal vascular pattern in which it is expected that a capillary network of microscopic vessels lies interposed between high-pressure arteries that deliver blood and thin-walled veins that collect low-pressure blood for return to the heart. In the case of arteriovenous malformations, arteries or arterioles connect directly to the venous collection system, bypassing any capillary bed. Clinical consequences result from rupture and hemorrhage, from dramatically increased blood flow, or from the loss of capillary functions such as nutrient exchange and filtering function. These malformations can occur sporadically or as a component of inherited vascular malformation syndromes. In these and other hereditary vascular malformation syndromes, genetic studies have identified proteins and pathways involved in vascular morphogenesis and development. A common theme observed is that vascular malformations result from disruption in pathways involved in vascular stability. Here we review the vascular malformations and pathways involved in hereditary hemorrhagic telangiectasia, capillary malformation-arteriovenous malformation, cerebral cavernous malformations, and mucocutaneous venous malformations.

Entities:  

Mesh:

Year:  2013        PMID: 23125071      PMCID: PMC3552339          DOI: 10.1101/cshperspect.a006635

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Med        ISSN: 2157-1422            Impact factor:   6.915


  59 in total

1.  Molecular cloning of cDNAs encoding the GAP-associated protein p190: implications for a signaling pathway from ras to the nucleus.

Authors:  J Settleman; V Narasimhan; L C Foster; R A Weinberg
Journal:  Cell       Date:  1992-05-01       Impact factor: 41.582

2.  Arteriovenous malformation in the buttock: treatment with a combination of selective embolization and excision.

Authors:  T Ishihara; M Hirooka; T Ono
Journal:  J Dermatol       Date:  1997-12       Impact factor: 4.005

3.  Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas.

Authors:  S Laberge-le Couteulx; H H Jung; P Labauge; J P Houtteville; C Lescoat; M Cecillon; E Marechal; A Joutel; J F Bach; E Tournier-Lasserve
Journal:  Nat Genet       Date:  1999-10       Impact factor: 38.330

Review 4.  Hereditary hemorrhagic telangiectasia.

Authors:  A E Guttmacher; D A Marchuk; R I White
Journal:  N Engl J Med       Date:  1995-10-05       Impact factor: 91.245

5.  A murine model of hereditary hemorrhagic telangiectasia.

Authors:  A Bourdeau; D J Dumont; M Letarte
Journal:  J Clin Invest       Date:  1999-11       Impact factor: 14.808

6.  Defective angiogenesis in mice lacking endoglin.

Authors:  D Y Li; L K Sorensen; B S Brooke; L D Urness; E C Davis; D G Taylor; B B Boak; D P Wendel
Journal:  Science       Date:  1999-05-28       Impact factor: 47.728

7.  Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22.

Authors:  I Serebriiskii; J Estojak; G Sonoda; J R Testa; E A Golemis
Journal:  Oncogene       Date:  1997-08-28       Impact factor: 9.867

8.  Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Authors:  D W Johnson; J N Berg; M A Baldwin; C J Gallione; I Marondel; S J Yoon; T T Stenzel; M Speer; M A Pericak-Vance; A Diamond; A E Guttmacher; C E Jackson; L Attisano; R Kucherlapati; M E Porteous; D A Marchuk
Journal:  Nat Genet       Date:  1996-06       Impact factor: 38.330

9.  Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

Authors:  K A McAllister; K M Grogg; D W Johnson; C J Gallione; M A Baldwin; C E Jackson; E A Helmbold; D S Markel; W C McKinnon; J Murrell
Journal:  Nat Genet       Date:  1994-12       Impact factor: 38.330

10.  Selective ablation of immature blood vessels in established human tumors follows vascular endothelial growth factor withdrawal.

Authors:  L E Benjamin; D Golijanin; A Itin; D Pode; E Keshet
Journal:  J Clin Invest       Date:  1999-01       Impact factor: 14.808

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  16 in total

1.  [Cavernomas of the central nervous system : Observational study of 111 patients].

Authors:  C Mayer; U M Mauer; G Bluhm; R Mathieu; C Hackenbroch; S Mayer
Journal:  Nervenarzt       Date:  2018-02       Impact factor: 1.214

2.  Constitutively active Notch4 receptor elicits brain arteriovenous malformations through enlargement of capillary-like vessels.

Authors:  Patrick A Murphy; Tyson N Kim; Lawrence Huang; Corinne M Nielsen; Michael T Lawton; Ralf H Adams; Chris B Schaffer; Rong A Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-02       Impact factor: 11.205

3.  Excess vascular endothelial growth factor-A disrupts pericyte recruitment during blood vessel formation.

Authors:  Jordan Darden; Laura Beth Payne; Huaning Zhao; John C Chappell
Journal:  Angiogenesis       Date:  2018-09-20       Impact factor: 9.596

4.  The use of sodium tetradecyl sulphate for the treatment of venous malformations of the head and neck.

Authors:  Xena Alakailly; Raja Kummoona; Faisal A Quereshy; Dale A Baur; Ariadne E González
Journal:  J Maxillofac Oral Surg       Date:  2014-03-11

Review 5.  Genetics of brain arteriovenous malformations and cerebral cavernous malformations.

Authors:  Hiroki Hongo; Satoru Miyawaki; Yu Teranishi; Daiichiro Ishigami; Kenta Ohara; Yu Sakai; Daisuke Shimada; Motoyuki Umekawa; Satoshi Koizumi; Hideaki Ono; Hirofumi Nakatomi; Nobuhito Saito
Journal:  J Hum Genet       Date:  2022-07-13       Impact factor: 3.755

Review 6.  Molecular and genetic mechanisms in brain arteriovenous malformations: new insights and future perspectives.

Authors:  Sandra Vetiska; Thomas Wälchli; Ivan Radovanovic; Moncef Berhouma
Journal:  Neurosurg Rev       Date:  2022-10-11       Impact factor: 2.800

7.  Case Report: A Rare Abdominopelvic Arteriovenous Malformation: Originating From Splenic Artery and Draining Into Portal Vein.

Authors:  Xin Li; Jiehua Li; Mo Wang; Junwei Wang; Lunchang Wang; Hao He; Ming Li; Quanming Li; Chang Shu
Journal:  Front Cardiovasc Med       Date:  2022-06-23

8.  Quantitative analysis of retinal intermediate and deep capillary plexus in patients with retinal deep vascular complex ischemia.

Authors:  Xin-Xin Li; Tian-Wei Qian; Ya-Nan Lyu; Xun Xu; Su-Qin Yu
Journal:  Int J Ophthalmol       Date:  2021-07-18       Impact factor: 1.779

9.  Biological relevance of tissue factor and IL-6 in arteriovenous malformations.

Authors:  Shouhei Noshiro; Takeshi Mikami; Yuko Kataoka-Sasaki; Masanori Sasaki; Kazuo Hashi; Shunya Ohtaki; Masahiko Wanibuchi; Nobuhiro Mikuni; Jeffery D Kocsis; Osamu Honmou
Journal:  Neurosurg Rev       Date:  2016-08-19       Impact factor: 3.042

Review 10.  To be or not to be: endothelial cell plasticity in development, repair, and disease.

Authors:  Leah J Greenspan; Brant M Weinstein
Journal:  Angiogenesis       Date:  2021-01-15       Impact factor: 9.596

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