Coagulation disorders in patients with venous malformation of the limbs and trunk: A case series of 118 patients

Archives of Dermatology

Volumn 144, Issue 7, 2008, Pages 861-867

  Mazoyer, Elisabeth ^a,b   Enjolras, Odile ^a,c,e   Bisdorff, Annouk ^a   Perdu, Jérome ^a,d   Wassef, Michel ^a   Drouet, Ludovic ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b AVICENNE HOSPITAL   (France)

^c ARMAND TROUSSEAU HOSPITAL   (France)

^d HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^e ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

D DIMER; GADOLINIUM; VON WILLEBRAND FACTOR;

ADOLESCENT; ADULT; AGED; ARM; ARTICLE; BLOOD CLOTTING DISORDER; BLOOD CLOTTING TEST; CHILD; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; FEMALE; HUMAN; LABORATORY TEST; LEG VEIN; MAJOR CLINICAL STUDY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OUTCOME ASSESSMENT; PRIORITY JOURNAL; SCORING SYSTEM; SYMPTOMATOLOGY; TRUNK; VEIN MALFORMATION;

ADOLESCENT; ADULT; AGED; BLOOD COAGULATION DISORDERS; CHILD; CHILD, PRESCHOOL; EXTREMITIES; FEMALE; FRANCE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; JOINTS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; PAIN MEASUREMENT; SEVERITY OF ILLNESS INDEX; SEX FACTORS; VASCULAR MALFORMATIONS;

EID: 47849114345     PISSN: 0003987X     EISSN: 0003987X     Source Type: Journal    
DOI: 10.1001/archderm.144.7.861     Document Type: Article

References (17)

1. Wassef M, Enjolras O. Les malformations vasculaires superficielles: classification et histopathologie. Ann Pathol. 1999;19(3):253-264.
2. Wassef M, Vanwijck R, Clapuit P, Boon LM, Magalon G. Tumeurs et malformations vasculaires, classification anatomopathologique et imagerie. Ann Chir Plast Esthet. 2006;51(4-5):263-281.
3. Boon LM, Mulliken JB, Enjolras O, Vikkula M. Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities. Arch Dermatol. 2004;140(8):971-976.
4. Boon LM, Mulliken JB, Vikkula M, et al. Assignment of a locus for dominantly inherited venous malformation to chromosome 9p. Hum Mol Genet. 1994; 3(9):1583-1587.
5. Vikkula M, Boon LM, Carraway KL III, et al. Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2. Cell. 1996;87 (7):1181-1190.
6. Enjolras O, Mulliken JB. Vascular tumors and vascular malformations (new issues). Adv Dermatol. 1997;13:375-423.
7. Burrows PE, Laor T, Paltiel H, Robertson RL. Diagnostic imaging in the evaluation of vascular birthmarks. Dermatol Clin. 1998;16(3):455-488.
8. Dubois J, Garel L, Grignon A, et al. Imaging of hemangiomas and vascular malformations in children. Acad Radiol. 1998;5(5):390-400.
9. Paltiel HJ, Burrows PE, Kozakewich HP, Zurakowski D, Mulliken JB. Soft-tissue vascular anomalies: utility of US for diagnosis. Radiology. 2000;214(3):747-754.
10. Enjolras O, Ciabrini D, Mazoyer E, Laurian C, Herbreteau D. Extensive pure venous malformations in the upper or lower limb: a review of 27 cases. J Am Acad Dermatol. 1997;36(2, pt 1):219-225.
11. Mazoyer E, Enjolras O, Laurian C, Houdart E, Drouet L. Coagulation abnormalities associated with extensive venous malformations of the limbs: differentiation from Kasabach-Merritt syndrome. Clin Lab Haematol. 2002;24(4):243-251.
12. Enjolras O, Wassef M, Chapot R. A Color Atlas of Vascular Tumors and Vascular Malformations. New York, NY: Cambridge University Press; March 2007.
13. Enjolras O, Wassef M, Mazoyer E, et al. Infants with Kasabach-Merritt syndrome do not have "true" hemangioma. J Pediatr. 1997;130(4):631-640.
14. Enjolras O, Mulliken JB, Wassef M, et al. Residual lesions after Kasabach-Merritt phenomenon in 41 patients. J Am Acad Dermatol. 2000;42(2, pt 1):225-235.
15. Canataroglu A, Gumurdulu Y, Gumurdulu D, Balal M, Tuncer I, Sagliker Y. Coexistence of cystic intra abdominal lymphogiomas and diffuse venous haemangiomas in adult life. Neth J Med. 2003;61(3):95-97.
16. Bernathova M, Jaschke W, Pechlahner C, Zelger B, Bodner G. Primary angiosarcoma of the breast associated with Kasabach-Merritt syndrome during pregnancy. Breast. 2006;15(2):255-258.
17. Keeney S, Cummings AM. The molecular biology of von Willebrand disease. Clin Lab Haematol. 2001;23(4):209-230.