Colangiocarcinoma hiliar (tumor de Klatskin)
نویسندگان
چکیده
منابع مشابه
EXTRAHEPATIC BILIARY CYSTADENOCARCINOMA MIMICKING KLATSKIN TUMOR Cistoadenocarcinoma biliar extra-hepático mimetizando tumor de Klatskin
Biliary cystadenocarcinoma (BCAC) is a very rare malignant cystic neoplasm. Some authors think this particular neoplasm was conversion of biliary cystadenoma over several years of evolution. In the majority of the cases, it habitually occurs in the liver parenchyma (intrahepatic cystadenocarcinoma); sometimes can be observed extrahepatic biliary origin3,4,6,7,8,10,11 extrahepatic biliary cystad...
متن کاملHilar Cholangiocarcinoma (Klatskin tumor)
......................................... Received: 23-05-11 Accepted: 01-06-11 Abstract This is a clinical case of a 71-year-old man with an obstructive lesion of the hepatic hilum, the clinical, imaging studies and the lab tests suggest a Klatskin tumor, which was managed by percutaneous biliary drainage to relieve the jaundice. In this review we consider the pathogenetic factors of these tum...
متن کاملExtrahepatic bile duct neurilemmoma mimicking Klatskin tumor.
Neurilemmoma rarely develops in the biliary tree. Here, we report a 39-year-old Iranian woman with neurilemmoma in the extrahepatic bile duct presenting with progressively deepening jaundice. On the basis of clinical and radiological features, this tumor was initially suspected as Klatskin tumor. Histologically, the tumor was a typical neurilemmoma. Immunostaining showed that tumor cells were s...
متن کاملKlatskin tumor--results of surgical therapy.
Between January 1st 1990 and December 31st 1999, 24 patients affected by Klatskin tumor underwent operation in our department of surgery. According to Bismuth's classification, there were 0 (0%) type I, 5 (21%) type II, 6 (25%) type IIIa, 4 (17%) type IIIb and 9 (37%) type IV tumors. Five patients (21%) were treated by curative resection (group I) while in 14 patients (58%) palliative surgical ...
متن کاملAutoimmune cholangitis mimicking a klatskin tumor: a case report
INTRODUCTION Autoimmune cholangitis remains an elusive manifestation of immunoglobulin G4-associated systemic disease most commonly encountered in patients with autoimmune pancreatitis. No strict diagnostic criteria have been described to date and diagnosis mainly relies on a combination of clinical and histopathologic findings. It is hence even more challenging to diagnose autoimmune cholangit...
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ژورنال
عنوان ژورنال: Revista Clínica de Medicina de Familia
سال: 2014
ISSN: 1699-695X
DOI: 10.4321/s1699-695x2014000100013