1. Gastrointestinal Manifestations of Autosomal-Dominant Polycystic Kidney Disease 
Adam E. Mikolajczyk, Helen S. Te, Arlene B. Chapman 
Clinical Gastroenterology and Hepatology 
Volume 15, Issue 1, Pages (January 2017)
DOI: /j.cgh
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2. Figure 1
The Gigot Criteria for classifying polycystic liver disease. Type I is characterized by a liver that has <10 large (>10 cm) cysts. Type II is characterized by diffuse parenchymal involvement by multiple medium-sized cysts with large areas of noncystic parenchyma. Type III is characterized by large numbers of small and medium-sized cysts spread diffusely throughout the parenchyma with only minimal, normal areas.
Clinical Gastroenterology and Hepatology  , 17-24DOI: ( /j.cgh )
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3. Figure 2
Algorithm for the medical and surgical management of polycystic liver disease, which incorporates the Schnelldorfer classification (types A–D).
TACE, transarterial chemotherapy embolization.
Clinical Gastroenterology and Hepatology  , 17-24DOI: ( /j.cgh )
Copyright © 2017 AGA Institute Terms and Conditions