Tando
Online ISSN : 1883-6879
Print ISSN : 0914-0077
ISSN-L : 0914-0077
Case Reports
Three cases of Biliary Neuroendocrine Tumor
Hiroyuki MatsubayashiHirotoshi IshiwatariRyo AshidaKatsuhisa OgiYusuke YamamotoYukiyasu OkamuraTakaaki ItohTeichi SugiuraKeiko SasakiYuko KakudaKatsuhiko Uesaka
Author information
JOURNAL FREE ACCESS

2020 Volume 34 Issue 2 Pages 205-213

Details
Abstract

Medical information about neuroendocrine tumors (NETs) of the bile duct is incomplete due to their rarity. We herein report three cases of bile duct NETs. Case 1: CT demonstrated an isovascular mass in the lower bile duct. A transpapillary biopsy revealed neuroendocrine carcinoma (NEC). A pancreatoduodenectomy (PD) was performed, followed by adjuvant chemotherapy (CPT-11+CDDP); however, the patient died due to disease progression 32 months later. Case 2: A well-enhanced hepatic hilar tumor, not definitively diagnosed by the forceps biopsy, was resected and pathologically diagnosed as a NET (G2). Case 3: CT showed a 38mm, ill-enhanced tumor in the lower bile duct. A transpapillary forceps biopsy showed adenocarcinoma; however, the surgical specimens demonstrated NEC. Adequate tissue acquisition is necessary for the diagnosis of bile duct NEC.

Content from these authors
© 2020 Japan Biliary Association
Previous article Next article
feedback
Top