Combined and complex vascular malformations

被引：18

作者：

Clemens, Robert K. ^{[1
]}

Pfammatter, Thomas ^{[2
]}

Meier, Thomas O. ^{[1
]}

Alomari, Ahmad I. ^{[3
,4
,5
]}

Amann-Vesti, Beatrice R. ^{[1
]}

机构：

[1] Univ Zurich Hosp, Clin Angiol, CH-8091 Zurich, Switzerland

[2] Univ Zurich Hosp, Inst Diagnost & Intervent Radiol, CH-8091 Zurich, Switzerland

[3] Boston Childrens Hosp, Div Vasc & Intervent Radiol, Boston, MA USA

[4] Boston Childrens Hosp, Vasc Anomalies Ctr, Boston, MA USA

[5] Harvard Univ, Sch Med, Cambridge, MA 02138 USA

来源：

VASA-EUROPEAN JOURNAL OF VASCULAR MEDICINE | 2015年 / 44卷 / 02期

关键词：

Vascular malformation; combined vascular malformation; complex vascular malformation fibro-adipose vascular anomaly; central conducting lymphatic anomalies; KLIPPEL-TRENAUNAY-SYNDROME; STURGE-WEBER-SYNDROME; ENDOVENOUS LASER TREATMENT; CAPILLARY MALFORMATION; MAFFUCCIS-SYNDROME; RASA1; MUTATIONS; ARTERIOVENOUS MALFORMATION; PULMONARY-EMBOLISM; PROTEUS-SYNDROME; VENOUS INSUFFICIENCY;

D O I：

10.1024/0301-1526/a000414

中图分类号：

R6 [外科学];

学科分类号：

1002 ; 100210 ;

摘要：

The correct diagnosis of vascular malformations is obtainable by clinical assessment and patient history in the majority of cases. Nonetheless, confusion in nomenclature, existence of multiple classifications and rarity of these lesions leads to misdiagnosis and related wrong treatment. This is especially the case in combined or complex vascular malformations or vascular malformations that are part of syndromes as these have overlapping clinical and imaging features. New entities in the field of vascular anomalies have been described recently like fibro-adipose vascular anomaly or central conducting lymphatic anomalies.

引用

页码：92 / 105

页数：14

共 75 条

[1] PRIMARY CHYLOPERICARDIUM [J].

AKAMATSU, H ;

AMANO, J ;

SAKAMOTO, T ;

SUZUKI, A .

ANNALS OF THORACIC SURGERY, 1994, 58 (01) :262-266

[2] Complex Spinal-Paraspinal Fast-Flow Lesions in CLOVES Syndrome: Analysis of Clinical and Imaging Findings in 6 Patients [J].

Alomari, A. I. ;

Chaudry, G. ;

Rodesch, G. ;

Burrows, P. E. ;

Mulliken, J. B. ;

Smith, E. R. ;

Fishman, S. J. ;

Orbach, D. B. .

AMERICAN JOURNAL OF NEURORADIOLOGY, 2011, 32 (10) :1812-1817

[3] Fibro-Adipose Vascular Anomaly: Clinical-Radiologic-Pathologic Features of a Newly Delineated Disorder of the Extremity [J].

Alomari, Ahmad I. ;

Spencer, Samantha A. ;

Arnold, Ryan W. ;

Chaudry, Gulraiz ;

Kasser, James R. ;

Burrows, Patricia E. ;

Govender, Pradeep ;

Padua, Horacio M. ;

Dillon, Brian ;

Upton, Joseph ;

Taghinia, Amir H. ;

Fishman, Steven J. ;

Mulliken, John B. ;

Fevurly, Rebecca D. ;

Greene, Arin K. ;

Landrigan-Ossar, Mary ;

Paltiel, Harriet J. ;

Trenor, Cameron C., III ;

Kozakewich, Harry P. .

JOURNAL OF PEDIATRIC ORTHOPAEDICS, 2014, 34 (01) :109-117

[4] CLOVES syndrome with thoracic and central phlebectasia: Increased risk of pulmonary embolism [J].

Alomari, Ahmad I. ;

Burrows, Patricia E. ;

Lee, Edward Y. ;

Hedequist, Daniel J. ;

Mulliken, John B. ;

Fishman, Steven J. .

JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2010, 140 (02) :459-463

[5] Diversion Venography-A Modified Technique in Klippel-Trenaunay Syndrome: Initial Experience [J].

Alomari, Ahmad I. .

JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2010, 21 (05) :685-689

[6] Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2 [J].

Amary, M. Fernanda ;

Damato, Stephen ;

Halai, Dina ;

Eskandarpour, Malihe ;

Berisha, Fitim ;

Bonar, Fiona ;

McCarthy, Stan ;

Fantin, Valeria R. ;

Straley, Kimberly S. ;

Lobo, Samira ;

Aston, Will ;

Green, Claire L. ;

Gale, Rosemary E. ;

Tirabosco, Roberto ;

Futreal, Andrew ;

Campbell, Peter ;

Presneau, Nadege ;

Flanagan, Adrienne M. .

NATURE GENETICS, 2011, 43 (12) :1262-U129

[7] Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations [J].

Amyere, Mustapha ;

Aerts, Virginie ;

Brouillard, Pascal ;

McIntyre, Brendan A. S. ;

Duhoux, Francois P. ;

Wassef, Michel ;

Enjolras, Odile ;

Mulliken, John B. ;

Devuyst, Olivier ;

Antoine-Poirel, Helene ;

Boon, Laurence M. ;

Vikkula, Miikka .

AMERICAN JOURNAL OF HUMAN GENETICS, 2013, 92 (02) :188-196

[8] Maffucci lymphangioma syndrome: an unusual variant of Ollier's disease, a case report and a review of the literature [J].

Auyeung, J ;

Mohanty, K ;

Tayton, K .

JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B, 2003, 12 (02) :147-150

[9] MULTIPLE SARCOMAS IN MAFFUCCIS SYNDROME [J].

BANNA, M ;

PARWANI, GS .

BRITISH JOURNAL OF RADIOLOGY, 1969, 42 (496) :304-&

[10] THE KLIPPEL-TRENAUNAY SYNDROME - CLINICAL, RADIOLOGICAL AND HEMODYNAMIC FEATURES AND MANAGEMENT [J].

BASKERVILLE, PA ;

ACKROYD, JS ;

THOMAS, ML ;

BROWSE, NL .

BRITISH JOURNAL OF SURGERY, 1985, 72 (03) :232-236

← 1 2 3 4 5 6 7 8 →