Renal lymphangiomatosis, interrupted IVC with persistent primitive hepatic venous plexus and multiple anomalous venous channels: parts of an overlap syndrome?-Reference-Cited by-同舟云学术

Renal lymphangiomatosis, interrupted IVC with persistent primitive hepatic venous plexus and multiple anomalous venous channels: parts of an overlap syndrome?

Published:2011-07-20 Issue:2 Volume:42 Page:253-256
ISSN:0301-0449
Container-title:Pediatric Radiology
language:en
Short-container-title:Pediatr Radiol

Author:

Watson Tom,Martinez Ester,Crabbe David,Chetcuti Phillip,Kraft Jeannette K.

Publisher

Springer Science and Business Media LLC

Subject

Radiology Nuclear Medicine and imaging,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00247-011-2184-2.pdf

Reference8 articles.

1. Vissers W, Van Steensel M, Steijlen P et al (2003) Klippel-Trenaunay syndrome and Sturge-Weber syndrome: variations on a theme? Eur J Dermatol 13:238–241

2. Garzon MC, Huang JT, Enjolras O et al (2007) Vascular malformations. Part II: associated syndromes. J Am Acad Dermatol 56:541–564. doi: 10.1016/j.jaad.2006.05.066

3. Telander RL, Kaufman BH, Gloviczki P et al (1984) Prognosis and management of lesions of the trunk in children with Klippel-Trenaunay Syndrome. J Pediatr Surg 19:417–422. doi: 10.1016/S0022-3468(84)80266-3

4. Darwish K, Bleau BL (1998) Extensive small bowel varices as a cause of severe anemia in Klippel-Trenaunay-Weber Syndrome. Am J Gastroenterol 93:2274–2275

5. Verma A, Gupta RK, Kumar S et al (2006) Non-invasive imaging of persistent primitive hepatic venous plexus using doppler sonography and magnetic resonance imaging. Eur J Rad Extra 60:69–73. doi: 10.1016/j.ejrex.2006.09.002

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