Persistent Hepatic Venous Plexus in a Patient with Sturge-Weber Syndrome
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2008.00722.x/fullpdf
Reference10 articles.
1. Klippel-Trenaunay syndrome: the importance of “geographic stains” in identifying lymphatic disease and risk of complications;Maari;J Am Acad Dermatol,2004
2. Vascular anomalies in Proteus syndrome;Hoeger;Clin Exp Dermatol,2004
3. Bleeding from cavernous angiomatosis of the rectum in Klippel-Trenaunay syndrome: report of three cases and literature review;Wilson;Am J Gastroenterol,2001
4. Sturge-Weber and Klippel-Trenaunay syndromes with absence of inferior vena cava;Stewart;Arch Dis Child,1990
5. Angiographic findings of persistent primitive hepatic venous plexus;McDonald;AJR,2000
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3. Tumor-Like Vascular Malformations;Tumors and Tumor-Like Lesions of the Hepatobiliary Tract;2016
4. Persistent primitive hepatic venous plexus with Scimitar syndrome: description of a case and review of the literature;Cardiology in the Young;2014-09-24
5. Renal lymphangiomatosis, interrupted IVC with persistent primitive hepatic venous plexus and multiple anomalous venous channels: parts of an overlap syndrome?;Pediatric Radiology;2011-07-20
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