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Vascular access for chronic hemodialysis in a patient with epidermolysis bullosa dystrophica H allopeau‐ S iemens

2012; Wiley; Volume: 17; Issue: 1 Linguagem: Inglês

10.1111/j.1542-4758.2012.00699.x

1542-4758

Sanja Sakan, Nikolina Bašić‐Jukić, Boris Tomašević, Petar Kes, Daniela Bandić Pavlović, Mladen Perić,

Genetic and rare skin diseases.

Abstract Epidermolysis bullosa is a rare genetic hereditary disease characterized with mechanobullous dermatosis. Except cutaneous, these patients have various extracutaneous manifestations and some types of epidermolysis bullosa comprise almost all organ systems. Because of prolonged life span, chronic renal insufficiency has become an important cause of morbidity and death in these patients. Establishment of functional vascular dialysis access is a great challenge for both the doctors and the patients. Multidisciplinary approach is essential. We present a case of successful establishment of dialysis access via T esio catheter in a young woman suffering from epidermolysis bullosa dystrophica H allopeau‐ S iemens and end‐stage renal disease. Since then, the T esio catheter inserted via the right internal jugular vein has been the functional mean of dialysis. The patient was given the opportunity to lead a quality and active life in spite of disabling disease. Several cases of successful dialysis access establishment with dialysis catheters via central veins have been reported. We report the successful establishment of long‐term dialysis access via T esio catheter and suggest this approach as ideal for these patients. This is the first report dealing with vascular access in this group of patients.