1.Primary hepatic tuberculosis mimicking intrahepatic cholangiocarcinoma: report of two cases.
Annals of Surgical Treatment and Research 2015;89(2):98-101
Hepatic tuberculosis (TB) is usually associated with pulmonary or miliary TB, but primary hepatic TB is very uncommon even in countries with high prevalence of TB. The clinical manifestation of primary hepatic TB is atypical and imaging modalities are unhelpful for differential diagnosis of the liver mass. Image-guided needle biopsy is the best diagnostic method for primary hepatic TB. In the cases presented here, we did not perform liver biopsy because we believed the liver masses were cholangiocarcinoma, but primary hepatic TB was ultimately confirmed by postoperative pathology. Here we report two cases of patients who were diagnosed with primary hepatic TB mimicking mass-forming intrahepatic cholangiocarcinoma.
Biopsy
;
Biopsy, Needle
;
Cholangiocarcinoma*
;
Diagnosis, Differential
;
Hepatectomy
;
Humans
;
Liver
;
Pathology
;
Prevalence
;
Tuberculosis
;
Tuberculosis, Hepatic*
;
Cholangiocarcinoma
2.Intraductal Intrahepatic Cholangiocarcinoama.
The Korean Journal of Hepatology 2003;9(1):47-48
No abstract available.
Aged
;
*Bile Duct Neoplasms/diagnosis/pathology
;
*Bile Ducts, Intrahepatic
;
*Cholangiocarcinoma/diagnosis/pathology
;
Humans
;
Male
3.A Case of Combined Hepatocellular-Cholangiocarcinoma with Underlying Schistosomiasis.
Chang Kyun HONG ; Jin Mo YANG ; Bong Koo KANG ; Jin Dong KIM ; Young Chul KIM ; U Im CHANG ; Jin Young YOO
The Korean Journal of Internal Medicine 2007;22(4):283-286
Combined hepatocellular-cholangiocarcinoma is a rare form of primary liver cancer showing features of both hepatocellular and biliary epithelial differentiation. We report here on a case with collision tumor, which apparently was the coincidental occurrence of both hepatocellular carcinoma and cholangiocarcinoma underlying schistosomiasis. A 39-year-old-Philippine female was transferred to our hospital for evaluation of a liver mass that was found on ultrasonography at a local hospital. HBsAg and Anti-HCV were negative and serum alpha-fetoprotein (AFP) level was normal. The tumor mass was histologically diagnosed as adenocarcinoma by sono-guided biopsy before the operation. Partial lobectomy was performed and we histologically identified the concurrent occurrence of hepatocellular carcinoma and cholangiocarcinoma, (a "collision type carcinoma").
Adenocarcinoma/diagnosis/pathology/surgery
;
Adult
;
Carcinoma, Hepatocellular/*diagnosis/pathology/surgery
;
Cholangiocarcinoma/*diagnosis/pathology/surgery
;
Female
;
Humans
;
Schistosomiasis/*physiopathology
4.Papillary Cholangiocarcinoma Arising from Biliary Papillomatosis.
The Korean Journal of Hepatology 2007;13(2):239-242
No abstract available.
Aged
;
Bile Duct Neoplasms/*diagnosis/pathology
;
*Bile Ducts, Intrahepatic
;
Carcinoma, Papillary/*diagnosis/pathology
;
Cholangiocarcinoma/*diagnosis/pathology
;
Female
;
Humans
6.Combined Hepatocellular-cholangiocarcinoma.
The Korean Journal of Hepatology 2007;13(4):571-575
7.Histopathology of a benign bile duct lesion in the liver: Morphologic mimicker or precursor of intrahepatic cholangiocarcinoma.
Clinical and Molecular Hepatology 2016;22(3):400-405
A bile duct lesion originating from intrahepatic bile ducts is generally regarded as an incidental pathologic finding in liver specimens. However, a recent study on the molecular classification of intrahepatic cholangiocarcinoma has focused on the heterogeneity of this carcinoma and has suggested that the cells of different origins present in the biliary tree may have a major role in the mechanism of oncogenesis. In this review, benign intrahepatic bile duct lesions—regarded in the past as reactive changes or remnant developmental anomalies and now noted to have potential for developing precursor lesions of intrahepatic cholangiocarcinoma—are discussed by focusing on the histopathologic features and its implications in clinical practice.
Bile Duct Neoplasms/*pathology
;
Bile Ducts/pathology
;
Bile Ducts, Intrahepatic
;
Cholangiocarcinoma/*pathology
;
Diagnosis, Differential
;
Humans
;
Liver/pathology
9.Combined Hepatocellular-cholangiocarcinoma.
Joon Koo HAN ; Se Hyung KIM ; Soo Jin KIM
The Korean Journal of Hepatology 2007;13(1):112-115
10.A Case of Intrahepatic Sarcomatoid Cholangiocarcinoma Mimicking Liver Abscess.
Sung Min KONG ; Kwang Min KIM ; Jae Jin LEE ; Woong Pyo HONG ; Ik Sung CHOI ; Kye Hwa JEONG ; Byung Soo KWAN ; Dong Gyu LEE
Korean Journal of Pancreas and Biliary Tract 2016;21(3):174-179
Sarcomatoid transformation of intrahepatic cholangiocarcinoma is rarely found but usually has very poor prognosis due to the lack of effective approaches for early detection and its aggressive nature. We report a case of this tumor type, in a 60-year-old man who was referred to our hospital for further evaluation of screening-detected, asymptomatic hepatic lesion. Clinical diagnosis was elusive despite performance of different imaging modalities and a transcutaneous liver biopsy. Pathology of the surgically resected tumor demonstrated intrahepatic sarcomatoid cholangiocarcinoma. In our case, tumor cells expressed strong immunoreactivity to both cytokeratin-19 and vimentin. We assume the relatively good prognosis of this patient would be expected because surgery played a critical role at an early stage of the tumor.
Biopsy
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Cholangiocarcinoma*
;
Diagnosis
;
Humans
;
Keratin-19
;
Keratins
;
Liver Abscess*
;
Liver*
;
Middle Aged
;
Pathology
;
Prognosis
;
Vimentin