Osler-Weber-Rendu disease with esophageal varices and hepatic nodular change.

A 72-year-old male visited our hospital for further evaluation of esophageal varices. Telangiectasias were present in the stomach. He had recurrent epistaxis, which was also confirmed in his family's medical history. We diagnosed this case as Osler-Weber-Rendu disease. He had concomitant with hepatic nodular change. Abdominal angiography showed arterio-portal (A-P) shunts, superior mesenteric artery (SMA)-superior mesenteric vein (SMV) shunt, extension of SMV, and dilated and meandering portal vein. Esophageal varices were treated by endoscopic variceral ligation (EVL) and argon plasma coagulation (APC) therapy for prophylaxis of bleeding.

[1]  Liang‐Kung Chen,et al.  Hereditary hemorrhagic telangiectasia. , 2020, Zhonghua yi xue za zhi = Chinese medical journal; Free China ed.

[2]  K. Hörmann,et al.  Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures , 2006, Wiener klinische Wochenschrift.

[3]  E. Buscarini,et al.  Liver involvement in hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber disease. , 2005, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

[4]  T. Shioya,et al.  Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan , 2002, Human mutation.

[5]  D. Jain,et al.  Liver disease in patients with hereditary hemorrhagic telangiectasia. , 2000, The New England journal of medicine.

[6]  K. Hisamatsu,et al.  Peripheral arterial coil embolization for hepatic arteriovenous malformation in Osler-Weber-Rendu disease; useful for controlling high output heart failure, but harmful to the liver. , 1999, Internal medicine.

[7]  M. Manns,et al.  Clinical outcome of transfemoral embolisation in patients with arteriovenous malformations of the liver in hereditary haemorrhagic telangiectasia (Weber-Rendu-Osler disease) , 1998, Gut.

[8]  J. Lammers,et al.  Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease): new insights in pathogenesis, complications, and treatment. , 1996, Archives of internal medicine.

[9]  H. Plauchu,et al.  Hepatic involvement in hereditary hemorrhagic telangiectasia: clinical, radiological, and hemodynamic studies of 11 cases. , 1993, Gastroenterology.

[10]  T. Nostrant,et al.  Clinical manifestations of hereditary hemorrhagic telangiectasia. , 1984, The American journal of gastroenterology.

[11]  G. Martini The liver in hereditary haemorrhagic teleangiectasia: an inborn error of vascular structure with multiple manifestations: a reappraisal. , 1978, Gut.