Adenocarcinoma of the hepatic duct junction. A reappraisal of the histologic criteria of malignancy
Open Access
- 1 April 1984
- Vol. 53 (7), 1545-1551
- https://doi.org/10.1002/1097-0142(19840401)53:7<1545::aid-cncr2820530721>3.0.co;2-n
Abstract
The morphologic distinction between benign and malignant sclerotic processes involving the hepatic duct junction may be difficult. To determine reliable histologic criteria of malignancy, the authors reviewed 18 cases of clinically suspected adenocarcinoma of the hepatic duct junction (Klatskin tumor) retrieved from our autopsy and surgical pathology files over the last decade. The lesions were compared histologically to a variety of benign sclerotic biliary duct lesions, including four cases of primary sclerosing cholangitis (PSC) treated surgically over the same time period. A diagnosis of malignancy was confirmed histologically in 16 suspected Klatskin tumors, based on the presence of severe cytologic atypia (13) and/or perineural invasion (15). The tumor patients averaged 59 years of age with a male to female ratio of 2:1. Patients with segmental tumor resection and postoperative radiotherapy have survived as a group 6 months longer (average, 15.7 months) than those treated with drainage procedures alone (average, 9.5 months) (P < 0.005), but have had extensive postoperative morbidity. In all the surgical specimens, tumor was present at one or more margins of resection. Primary sclerosing cholangitis patients were younger (average, 31 years of age) with a similar male predominance, but with a strong history of inflammatory bowel disease. All are alive up to 6.5 years since disease onset, with comparatively little postoperative morbidity. Two clinically diagnosed Klatskin tumors were not confirmed on histologic review. Both patients are alive at 1 and 3.5 years following onset of disease, having experienced little postoperative morbidity. Data indicate that Klatskin tumors are relatively aggressive malignancies, distinct from more indolent benign sclerotic disease, but occasionally mimicked by it clinically. Malignancy can be diagnosed histologically with adequate tissue sampling, thereby facilitating clinical decisions regarding radiotherapy or other palliative surgical procedures.This publication has 17 references indexed in Scilit:
- Case 6-1982New England Journal of Medicine, 1982
- Diagnosis and treatment of primary extrahepatic bile duct tumorsThe American Journal of Surgery, 1982
- Prognostic Factors in Bile Duct CarcinomaAnnals of Surgery, 1981
- Carcinoma of the hepatic duct junctionBritish Journal of Surgery, 1981
- Sclerosis of the Extrahepatic Bile DuctsArchives of Surgery, 1974
- Sclerosing Carcinoma of the Hepatic Bile DuctsSurgical Clinics of North America, 1973
- Ulcerative colitis and carcinoma of the bile ductsThe American Journal of Surgery, 1971
- Adenocarcinoma of the hepatic duct at its bifurcation within the porta hepatisAmerican Journal Of Medicine, 1965
- Carcinoma of the hepatic ducts within the liverBritish Journal of Surgery, 1962
- Sclerosing Carcinoma of the Major Intrahepatic Bile DuctsArchives of Surgery, 1957