A Rare Cause of Recurrent Iron Deficiency Anemia: Osler Weber Rendu Syndrome

Year 2016, , 0 - 0, 15.03.2016

Aslı Korur , Çiğdem Gereklioğlu , Süheyl Asma , Nurhilal Büyükkurt Barış Soydaş Gürcan Erbay

https://doi.org/10.5455/tjfmpc.193253

Abstract

Osler-Weber-Rendu Syndrome (hereditary hemorrhagic telengiectasis) is a hereditary disease with autosomal dominant inheritance characterized by muco-cutaneous telengiectasis, arterio-venous malformations in internal organs. The disease is manifested by telengiectasis in oral mucosa, ear, nasal mucosa, fingertips and finger-beds and recurrent hemorrhage. Epistaxis is among the typical findings of the disease. Coexistence with arterio-venous malformations is common. It may lead to gastrointestinal hemorrhage and neurologic problems due to mucosal telengiectasis. Herein, we presented a case who had recurrent iron deficiency anemia and diagnosed with Osler-Weber-Rendu Syndrome as the result of radiologic and endoscopic examinations performed due to the presence of oral telengiectasis.

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