Neurofibromatosis with cholangiocarcinoma: A Case Report
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Case report

Neurofibromatosis with cholangiocarcinoma: A Case Report

Anatol J Gen Med Res 2015;25(3):209-211 DOI: 10.5222/terh.2015.209
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Abstract

Neurofibromatosis (NF) is rare in our country; skin, nervous system, or both holds together, is a heterogeneous disease hereditary. NF type I (Von Recklinghausen disease) 2500-3000 births constituting a monitoring and genetic susceptibility to the most common neoplasms. It is a neurocutaneous disease. In association with intrahepatic cholangiocarcinoma NF type it is rare. 36 Years intrahepatic diffuse neurofibromas on the whole body of our patients who were followed by cholangiocarcinoma diagnosed; back "cafe au lait" spots on the iris and "Lisch nodules" We've found. Thus our diagnosis of NF type 1 cases, we aim to share because of its rarity.

Keywords: Neurofibromatosis, cholangiocarcinoma, Lisch nodules