Zusammenfassung
Es handelt sich bei den Klatskin-Tumoren um eine Subgruppe der Gallengangkarzinome, die aufgrund ihrer besonderen Lokalisation eine chirurgische Herausforderung darstellt. Histomorphologisch zeigen Gallengangkarzinome keine lokalisationsabhängigen Unterschiede auch in Bezug auf ihre Vorläuferläsionen. Auch molekularbiologisch gibt es nur wenige Unterschiede. Wichtig für die Therapie und Prognoseabschätzung ist eine genau Diagnosestellung und bei Resektabilität eine standardisierte Aufarbeitung des Operationspräparats, um die Resektionsränder genau zu beurteilen. Ebenso wichtig ist eine regionäre Lymphknotendissektion. Molekularbiologisch sind bei dieser relativ seltenen Tumorerkrankung weitere Untersuchungen zu fordern, um eine individualisierte Therapie, wie sie derzeit für andere gastrointestinale Tumoren bereits durchgeführt wird, zu ermöglichen.
Abstract
Klatskin tumors are a distinct subgroup of cholangiocarcinomas which are a surgical challenge due to their special localization. Different localizations do not show great differences concerning histomorphology and precursor lesions. With respect to molecular alterations there are only small differences. Accurate clinical and histomorphological diagnosis is important for therapy and especially the prediction of prognosis as well as standardized processing of the resection specimen if the carcinoma is resectable. Additionally, accurate lymph node dissection is necessary. Concerning molecular markers further investigations are needed to develop individualized therapy regimes.
Literatur
Allen PJ, Reiner AS, Gonen M et al (2008) Extrahepatic cholangiocarcinoma: a comparison of patients with resected proximal and distal lesions. HPB 10:341–346
Anonymous (2003) General rules for surgical and pathological studies on cancers of biliary tract. Kanehara, Tokyo, Japan
Benckert C, Jonas S, Cramer T et al (2003) Transforming growth factor beta 1 stimulates vascular endothelial growth factor gene transcription in human cholangiocellular carcinoma cells. Cancer Res 63:1083–1092
Bismuth H, Corlette MB (1975) Intrahepatic cholangioenteric anastomosis in carcinoma of the hilus of the liver. Surg Gynecol Obstet 140:170–178
Bosman FT, Carneiro F, Hruban RH (Hrsg) (2010) WHO classification of tumours of the digestive system. World Health Organization
Deoliveira ML, Cunningham SC, Cameron JL et al (2007) Cholangiocarcinoma: thirty-one-year experience with 564 patients at a single institution. Ann Surg 245:755–762
Devaney K, Goodman ZD, Ishak KG (1994) Hepatobiliary cystadenoma and cystadenocarcinoma. A light microscopic and immunohistochemical study of 70 patients. Am J Surg Pathol 18:1078–1091
Endo K, Yoon BI, Pairojkul C et al (2002) ERBB-2 overexpression and cyclooxygenase-2 up-regulation in human cholangiocarcinoma and risk conditions. Hepatology 36:439–450
Esposito I, Schirmacher P (2008) Pathological aspects of cholangiocarcinoma. HPB 10:83–86
Gatto M, Alvaro D (2010) New insights on cholangiocarcinoma. World J Gastrointest Oncol 2:136–145
Jarnagin WR, Fong Y, Dematteo RP et al (2001) Staging, resectability, and outcome in 225 patients with hilar cholangiocarcinoma. Ann Surg 234:507–517
Klatskin G (1965) Adenocarcinoma of the hepatic duct at its bifurcation within the porta hepatis. An unusual tumor with distinctive clinical and pathological features. Am J Med 38:241–256
Kuroki T, Tajima Y, Matsuo K et al (2005) Genetic alterations in gallbladder carcinoma. Surg Today 35:101–105
Miller G, Socci ND, Dhall D et al (2009) Genome wide analysis and clinical correlation of chromosomal and transcriptional mutations in cancers of the biliary tract. J Exp Clin Cancer Res 28:62
Munding J, Tannapfel A (2011) Anatomy of the liver. What does the radiologist need to know? Radiologe 51:655–660
Murakami Y, Uemura K, Sudo T et al (2011) Prognostic factors after surgical resection for intrahepatic, hilar, and distal cholangiocarcinoma. Ann Surg Oncol 18:651–658
Nakazawa K, Dobashi Y, Suzuki S et al (2005) Amplification and overexpression of c-erbB-2, epidermal growth factor receptor, and c-met in biliary tract cancers. J Pathol 206:356–365
Nakeeb A, Pitt HA, Sohn TA et al (1996) Cholangiocarcinoma. A spectrum of intrahepatic, perihilar, and distal tumors. Ann Surg 224:463–473
Rashid A, Ueki T, Gao YT et al (2002) K-ras mutation, p53 overexpression, and microsatellite instability in biliary tract cancers: a population-based study in China. Clin Cancer Res 8:3156–3163
Rizzi PM, Ryder SD, Portmann B et al (1996) p53 Protein overexpression in cholangiocarcinoma arising in primary sclerosing cholangitis. Gut 38:265–268
Roa JC, Roa I, Correa P et al (2005) Microsatellite instability in preneoplastic and neoplastic lesions of the gallbladder. J Gastroenterol 40:79–86
Rocha FG, Matsuo K, Blumgart LH et al (2010) Hilar cholangiocarcinoma: the Memorial Sloan-Kettering Cancer Center experience. J Hepatobiliary Pancreat Sci 17:490–496
Sasaki R, Takeda Y, Funato O et al (2007) Significance of ductal margin status in patients undergoing surgical resection for extrahepatic cholangiocarcinoma. World J Surg 31:1788–1796
Schottenfeld D, Beebe-Dimmer J (2006) Chronic inflammation: a common and important factor in the pathogenesis of neoplasia. CA Cancer J Clin 56:69–83
Shimada K, Sano T, Sakamoto Y et al (2007) Surgical outcomes of the mass-forming plus periductal infiltrating types of intrahepatic cholangiocarcinoma: a comparative study with the typical mass-forming type of intrahepatic cholangiocarcinoma. World J Surg 31:2016–2022
Tannapfel A, Benicke M, Katalinic A et al (2000) Frequency of p16(INK4A) alterations and K-ras mutations in intrahepatic cholangiocarcinoma of the liver. Gut 47:721–727
Tannapfel A, Sommerer F, Benicke M et al (2003) Mutations of the BRAF gene in cholangiocarcinoma but not in hepatocellular carcinoma. Gut 52:706–712
Uenishi T, Hirohashi K, Kubo S et al (2001) Histologic factors affecting prognosis following hepatectomy for intrahepatic cholangiocarcinoma. World J Surg 25:865–869
Wise C, Pilanthananond M, Perry BF et al (2008) Mechanisms of biliary carcinogenesis and growth. World J Gastroenterol 14:2986–2989
Wittekind C, Meyer HJ (2010) TNM Klassifikation maligner Tumore. Wiley, Weinheim
Interessenkonflikt
Der korrespondierende Autor gibt an, dass kein Interessenkonflikt besteht.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Munding, J., Tannapfel, A. Anatomisch-pathologische Besonderheiten der Klatskin-Tumoren. Chirurg 83, 208–214 (2012). https://doi.org/10.1007/s00104-011-2175-8
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00104-011-2175-8