scholarly journals Management of a femoral diaphyseal fracture in a patient with Klippel-Trenaunay-Weber syndrome: a case report

Cases Journal ◽  
2009 ◽  
Vol 2 (1) ◽  
pp. 8852 ◽  
Author(s):  
Efstathios Tsaridis ◽  
Efthimios Papasoulis ◽  
Nikolaos Manidakis ◽  
Ioannis Koutroumpas ◽  
Savvas Lykoudis ◽  
...  
Keyword(s):  
Case Report ◽  
Diaphyseal Fracture ◽  
Weber Syndrome ◽  
Femoral Diaphyseal Fracture

Amputated limb by cerclage wire of femoral diaphyseal fracture: a case report

2016 ◽  
Vol 136 (12) ◽  
pp. 1691-1694 ◽  
Author(s):  
Yougun Won ◽  
Kyu-Hyun Yang ◽  
Kwang-kyoun Kim ◽  
M. J. Weaver ◽  
Elizabeth M. Allen
Keyword(s):  
Case Report ◽  
Diaphyseal Fracture ◽  
Cerclage Wire ◽  
Femoral Diaphyseal Fracture

71. Sturge–Weber syndrome + cortical dysplasia. A dual pathology case report

2016 ◽  
Vol 127 (9) ◽  
pp. e319
Author(s):  
Areli Rosario Suarez-Roman ◽  
Enoe Cruz-Martinez ◽  
Yokary Amor Mellado-Ortiz ◽  
Ernesto Ramirez-Navarrete ◽  
Paul Shkurovich-Bialik
Keyword(s):  
Case Report ◽  
Cortical Dysplasia ◽  
Dual Pathology ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome

scholarly journals Prenatal diagnosis of Klippel-Trenaunay-Weber syndrome: a case report

1992 ◽  
Vol 2 (5) ◽  
pp. 360-363 ◽  
Author(s):  
R. Heydanus ◽  
J. W. Wladimiroff ◽  
H. Brandenburg ◽  
J. L. J. Gaillard ◽  
P. A. Stewart ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Weber Syndrome

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

scholarly journals Report of a newborn with hemimegalencephaly in association with Klippel-Trenaunay-Weber syndrome

2005 ◽  
Vol 133 (1-2) ◽  
pp. 62-64
Author(s):  
Slobodan Obradovic ◽  
Biljana Vuletic ◽  
Andjelka Stojkovic-Andjelkovic ◽  
Zoran Igrutinovic
Keyword(s):  
Case Report ◽  
Soft Tissues ◽  
Varicose Veins ◽  
The Body ◽  
Arteriovenous Fistulae ◽  
Left Part ◽  
Weber Syndrome

Klippel-Trenaunay-Weber syndrome (KTW) is a rare phacomatosis whose main characteristics are: cutaneous angiomas (vascular nevi), varicose veins (arteriovenous fistulae) and hemihypertrophy of bones and soft tissues. This is a case report of KTW syndrome which was diagnosed in the first days of life on the basis of characteristic vascular nevi on the skin of the trunk and extremities in addition to hypertrophy of the left part of the body. Neuroradiologically verified hemimegalencephaly associated with temporal hemangioma represents a special particularity in our case. Measures of monitoring the child as well as stimulating and therapeutic actions were the issues of discussion.

scholarly journals Parkes-Weber syndrome in the emergency department

2021 ◽  
Vol 14 (9) ◽  
pp. e241649
Author(s):  
Raj Patel ◽  
Edward James Durant ◽  
Robert Freed
Keyword(s):  
Emergency Department ◽  
Interventional Radiology ◽  
Case Report ◽  
Vascular Malformations ◽  
Weber Syndrome ◽  
The Common ◽  
Work Up

This case report describes a 20-year-old woman presenting to the emergency department (ED) with unilateral leg swelling. After multiple visits to the ED and workups with rheumatology, dermatology, interventional radiology and genetics, she was finally diagnosed with Parkes-Weber syndrome. The purpose of this case report is to illustrate the common and uncommon presentations, mimickers and work-up of Parkes-Weber syndrome as well as provide a brief overview of vascular malformations in general.

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