Year 2015 / Volume 107 / Number 3
Notas
Ultrasound-guided percutaneous drainage and sclerotherapy in a patient with isolated autosomal dominant polycystic liver disease

178-181

Miguel ángel Sánchez Martos, José Manuel Gomis Díaz, José Manuel Sarabia Marín, Manuel Moya Ramón y Adolfo Aracil Marco

Abstract
Isolated polycystic liver disease (IPLD) is a rare genetic condition characterized by the presence of multiple liver cysts with no association with polycystic kidney disease. Most patients are asymptomatic and acute complications (cyst torsion, bleeding, infection) are uncommon. Imaging techniques, including abdominal ultrasounds, computerized axial tomography, and magnetic resonance imaging, represent a vital diagnostic modality. They are also useful for therapy support in this disease. Below we report a peculiar case of a female patient recently diagnosed with IPLD who, having received treatment with ultrasound- guided percutaneous drainage and sclerotherapy for a giant liver cyst, showed symptom and laboratory improvement.
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Miguel ángel Sánchez Martos, José Manuel Gomis Díaz, José Manuel Sarabia Marín, Manuel Moya Ramón y Adolfo Aracil Marco. Ultrasound-guided percutaneous drainage and sclerotherapy in a patient with isolated autosomal dominant polycystic liver disease. 178-181


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The Spanish Journal of Gastroenterology is the official organ of the Sociedad Española de Patología Digestiva, the Sociedad Española de Endoscopia Digestiva and the Asociación Española de Ecografía Digestiva
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