• S H Blaas, G Röckelein, J Wilke, J D Weinerth, J Dobroschke, J Schölmerich, and U Müller-Ladner.
• Klinik und Poliklinik für Innere Medizin I, Klinikum der Universität Regensburg. stefan.blaas@klinik.uni-regensburg.de
• Dtsch. Med. Wochenschr. 2006 Aug 18; 131 (33): 1803-6.

HistoryA 52-year-old woman with chronic anaemia presented with recurrent epistaxis, telangiectasias and haemangiomas, suggesting the presence of hereditary haemorrhagic telangiectasia (Osler-Rendu-Weber disease). Moreover, previous investigations had also shown multiple polyps of the stomach.InvestigationsA severe microcytic iron deficiency anaemia in combination with hepatic haemangiomas and duodenal angio-dysplasia were detected. Gastrointestinal endoscopy revealed multiple juvenile polyps in the gastric fundus and body, indicating the diagnosis of hereditary haemorrhagic telangiectasia in combination with juvenile polyposis.Therapy And CourseA gastrectomy was performed because of recurrent gastrointestinal bleeding and the malignant potential of juvenile gastric polyposis. Histopathology confirmed the diagnosis and did not reveal any malignancy.ConclusionThe association of hereditary haemorrhagic telangiectasia and juvenile polyposis, as seen in this patient, has been reported repeatedly. A diagnosis of one of the described entities should initiate the screening for evidence of the other one to prevent (life-threatening) complications.

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