1.Multidisciplinary Therapeutic Approach to Gallbladder Cancer
Korean Journal of Pancreas and Biliary Tract 2018;23(1):20-23
Gallbladder cancer is the most common of all the biliary tract cancers. Incidence gradually increases with age, and women are more likely diagnosed with gallbladder cancer. Patients with gallbladder cancer have poor prognosis due to early local and vascular invasion, extensive regional lymph node metastasis, and distant metastasis. Gallbladder cancer is also related with shorter median survival duration and shorter survival duration after recurrence in comparison with hilar cholangiocarcinoma. Complete removal with negative margins is considered as the only curative therapy for patients with gallbladder cancer. The optimal resection comprises cholecystectomy with a limited hepatic resection (segments IVB and V) and portal lymphadenectomy to include the tumor with negative margins. The optimum adjuvant therapy for patients with resected gallbladder cancer has not been confirmed. The greater benefit of radiation therapy was achieved in patients with T2 or greater stage tumors and node-positive disease. Primary options for patients with unresectable or metastatic diseases include: 1) clinical trial; 2) fluoropyrimidine-based or gemcitabine-based chemotherapy; or 3) best supportive care including biliary drainage. In patients with advanced stage and jaundice, biliary drainage should be considered before setting up chemotherapy.
Biliary Tract Neoplasms
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Cholecystectomy
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Drainage
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Drug Therapy
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Female
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Gallbladder Neoplasms
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Gallbladder
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Humans
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Incidence
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Jaundice
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Klatskin Tumor
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Lymph Node Excision
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Lymph Nodes
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Neoplasm Metastasis
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Prognosis
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Recurrence
2.Squamous Cell Carcinoma of the Extrahepatic Common Hepatic Duct
Myunghee KANG ; Na Rae KIM ; Dong Hae CHUNG ; Hyun Yee CHO ; Yeon Ho PARK
Journal of Pathology and Translational Medicine 2019;53(2):112-118
We report a rare case of hilar squamous cell carcinoma. A 62-year-old Korean woman complaining of nausea was referred to our hospital. Her biliary computed tomography revealed a 28 mm-sized protruding solid mass in the proximal common bile duct. The patient underwent left hemihepatectomy with S1 segmentectomy and segmental excision of the common bile duct. Microscopically, the tumor was a moderately differentiated squamous cell carcinoma of the extrahepatic bile duct, without any component of adenocarcinoma or metaplastic portion in the biliary epithelium. Immunohistochemically, the tumor was positive for cytokeratin (CK) 5/6, CK19, p40, and p63. Squamous cell carcinoma of the extrahepatic bile duct is rare. To date, only 24 cases of biliary squamous cell carcinomas have been reported. Here, we provide a clinicopathologic review of previously reported extrahepatic bile duct squamous cell carcinomas.
Adenocarcinoma
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Bile Ducts, Extrahepatic
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Carcinoma, Squamous Cell
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Common Bile Duct
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Drug Therapy
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Epithelial Cells
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Epithelium
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Female
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Hepatic Duct, Common
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Humans
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Keratins
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Klatskin Tumor
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Mastectomy, Segmental
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Middle Aged
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Nausea
3.Development of Brugada Syndrome Following Photodynamic Therapy in a Patient with Cholangiocarcinoma.
Duk Won BANG ; Min Su HYON ; Young Duk CHO ; Sung Koo KIM ; Young Joo KWON
The Korean Journal of Internal Medicine 2012;27(1):95-97
Brugada syndrome can be unmasked by several conditions including a febrile state, marked leukocytosis, and electrolyte disturbances. Herein, we describe a 62-year-old man with cholangiocarcinoma in the first reported case of Brugada syndrome onset following photodynamic therapy.
Bile Duct Neoplasms/*drug therapy
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*Bile Ducts, Intrahepatic
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Brugada Syndrome/diagnosis/*etiology/therapy
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Cardiopulmonary Resuscitation
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Cholangiocarcinoma/*drug therapy
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Electrocardiography
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Fatal Outcome
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Fever/etiology
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Humans
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Klatskin's Tumor/*drug therapy
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Male
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Middle Aged
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Photochemotherapy/*adverse effects
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Predictive Value of Tests
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Treatment Outcome
4.A Case of Undifferentiated (Embryonal) Liver Sarcoma Mimicking Klatskin Tumor in an Adult.
Ji Ae LEE ; Tae Wan KIM ; Jae Hoon MIN ; Sun Jung BYON ; Seung Hoon JANG ; Seung Yeon CHOI ; Hong Joo KIM
The Korean Journal of Gastroenterology 2010;55(2):144-148
Undifferentiated sarcoma is an uncommon primary malignant tumor of the liver typically occurring in older children. It is also referred to as malignant mesenchymoma, fibromyxosarcoma, or mesenchymal sarcoma. We experienced a case of undifferentiated sarcoma in 72-year-old male. Contrast enhanced liver CT scan revealed a 3.4 cm heterogeneously enhancing, ill-defined, and low attenuated mass in the left liver and subtle intrahepatic duct dilatation. And, in tubogram, there were segmental stenosis and occlusion from the hilum to the proximal common bile duct. We did ultrasonography guided liver biopsy. The pathologic finding revealed infiltrative growth of atypical cells with rhabdoid features. Some atypical cells showed clear cytoplasm, but no organoid pattern was identified. The stroma around atypical cells was filled with eosinophilic hyaline material. These tumor cells were positive for vimentin only, and the tumor was consistent with undifferentiated sarcoma of the liver.
Aged
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Bile Ducts, Intrahepatic/pathology
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Diagnosis, Differential
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Dilatation, Pathologic
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Humans
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Klatskin's Tumor/diagnosis
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Liver Neoplasms/*diagnosis/pathology/ultrasonography
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Male
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Positron-Emission Tomography
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Sarcoma/*diagnosis/pathology/ultrasonography
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Tomography, X-Ray Computed
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Tuberculosis/drug therapy/radiography
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Vimentin/metabolism