Telangiectasia affected Vater's papilla in Osler Rendu syndrome.
نویسندگان
چکیده
52-years-old male diagnosed of Rendu Osler syndrome (ROS) refered dark, pasty stools and anemia (Hg: 9 g/dl). The upper endoscopy revealed a duodenum mucosa with telangiectasias. Afterwards, an enteroscopy was performed and duodenum and jejunum telangiectasias were seen and treated by Argon plasma coagulation. During the procedure one telangiectasia that affected the entire Vater’s papilla (Fig. 1A) was identified and confirmed by duodenoscopy (Fig. 1B). The treatment of this particular lesion has been performed as follows: a bile duct cannulation and a subsequent sphincterotomy were done without any incidence. A plastic pancreatic stent was placed and then, the affected papilla’s area was treated by Argon coagu lation (Fig. 2A). A plastic biliary stent was placed finally. Four days after the procedure, both two stents were removed endoscopically and the disappearance of the papillary telangiectasia was confirmed (Fig. 2B). There were no early or late complications registered (period of follow up: 13 months). The patient has decreased the need for blood transfusions.
منابع مشابه
Osler-Weber-Rendu syndrome: a case report with familial clustering.
Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems. We present a case of Osler-Weber-Rendu syndrome with 11 affected members in her family.
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عنوان ژورنال:
- Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva
دوره 104 7 شماره
صفحات -
تاریخ انتشار 2012