Vascular access for chronic hemodialysis in a patient with epidermolysis bullosa dystrophica Hallopeau‐Siemens

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 rena...

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Veröffentlicht in:Hemodialysis international 2013-01, Vol.17 (1), p.126-129
Hauptverfasser: Sakan, Sanja, Basic‐Jukic, Nikolina, Tomasevic, Boris, Kes, Petar, Bandic Pavlovic, Daniela, Peric, Mladen
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Sprache:eng
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Zusammenfassung: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 Tesio catheter in a young woman suffering from epidermolysis bullosa dystrophica Hallopeau‐Siemens and end‐stage renal disease. Since then, the Tesio 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 Tesio catheter and suggest this approach as ideal for these patients. This is the first report dealing with vascular access in this group of patients.
ISSN:1492-7535
1542-4758
DOI:10.1111/j.1542-4758.2012.00699.x