Intrahepatic cholangiocarcinoma arising in autosomal dominant polycystic kidney disease [3]

Virchows Archiv

Volumn 441, Issue 1, 2002, Pages 98-100

  Sasaki, Motoko ^a   Katayanagi, Kazuyoshi ^a   Watanabe, Kishichiroh ^a   Takasawa, Kazuya ^a   Nakanuma, Yasuni ^a  

^a KANAZAWA UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCE   (Japan)

Author keywords

Intrahepatic cholangiocarcinoma; Polycystic kidney disease

Indexed keywords

TUMOR MARKER;

AGED; BILE DUCT CARCINOMA; CANCER INVASION; CASE REPORT; CHRONIC KIDNEY FAILURE; CLINICAL FEATURE; FAMILY HISTORY; HEMODIALYSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; KIDNEY HYPERTROPHY; KIDNEY POLYCYSTIC DISEASE; LABORATORY TEST; LETTER; MALE; PHYSICAL EXAMINATION; PRIORITY JOURNAL;

AGED; BILE DUCT NEOPLASMS; BILE DUCTS, INTRAHEPATIC; CHOLANGIOCARCINOMA; FATAL OUTCOME; HUMANS; MALE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT;

EID: 0036302423     PISSN: 09456317     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00428-002-0635-8     Document Type: Letter

References (10)

1. Cholangiocarcinoma in association with multiple biliary microhamartomas
2. Biology of polycystic kidney disease
3. Caroli's disease: A premalignant condition?
4. Risk factors of the development of hepatic cysts in autosomal dominant polycystic kidney disease
5. Bile duct carcinoma associated with multiple von Meyenburg complexes in the liver
6. Cholangiocellular carcinoma associated with multiple liver cysts
7. Cystic dilatation of peribiliary glands in livers with adult polycystic disease and livers with solitary nonparasitic cysts: An autopsy study
8. Pathology of cholangiocellular carcinoma
9. Intrahepatic peribiliary glands of humans. II Pathological spectrum
10. Hilar cholangiocarcinoma (Klatskin Tumor) arising from intrahepatic peribiliary glands