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The Korean Journal of Gastroenterology ; : 301-305, 2013.
Article in Korean | WPRIM | ID: wpr-171341

ABSTRACT

Neuroendocrine tumors of the extrahepatic biliary tree are extremely rare malignancies accounting for 0.2-2.0% of all gastrointestinal carcinoid tumors. Neuroendocrine tumors obstructing the biliary tree are extremely difficult to diagnose preoperatively and nearly impossible to differentiate from cholangiocarcinoma. Statistically, the most common anatomic location in the biliary tree is the common bile duct, followed by the perihilar region. Herein, we present a case of a small cell neuroendocrine carcinoma of the hilum in a 79-year-old man following laparotomy. To our knowledge, this is the first case of small cell type neuroendocrine carcinoma of hilar bile duct reported in Korea.


Subject(s)
Aged , Humans , Male , Bile Duct Neoplasms/diagnosis , Cholangiopancreatography, Endoscopic Retrograde , Diagnosis, Differential , Hepatic Duct, Common/pathology , Neuroendocrine Tumors/diagnosis , Tomography, X-Ray Computed
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