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Intrahepatic clear cell cholangiocarcinoma

Date:
June 2, 2010
Source:
World Journal of Gastroenterology
Summary:
Clear cell intrahepatic cholangiocarcinoma is a rare cancer. There is not enough information about the patients' underlying diseases, choice of treatment and prognosis. A Japanese medical team reported a rare case with detailed radiologic and pathologic examination and a comparison with previous reports. The cancer behaves as a low malignancy, but information is still lacking. Therefore, careful follow-up and acquisition of cases are necessary.

Intrahepatic cholangiocarcinoma (ICC) is a cancer of the bile duct in the liver. The clear cell subtype of ICC is a rare cancer; until now, only 8 cases have been reported. The number of reports is so small that a detail description of clear cell ICC is valuable.

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A case report will be published on May 28, 2010 in the World Journal of Gastroenterology addresses this question. The diagnostic pathology team led by Associate Professor Dr. Hayashi at the Department of Pathology, Nagasaki University Hospital in Japan collaborated with Professor Nagayasu, Department of the 1st Surgery and Professor Uetani, Department of Radiology, to investigate how the specific "clear cell" change occurs, a patient's underlying disease and choice of chemotherapy, and the prognosis for future patients of this rare cancer.

The patient was a 56-year-old Japanese man with a 3-year histry of hepatitis B virus (HBV) infection. The follow-up echo revealed a tumor of the liver. CT and MRI suggested hepatocellular carcinoma (HCC); a cancer of liver cells. The patient had surgery and the tumor was diagnosed as the rare "clear cell ICC," not a conventional HCC.

Unlike reported cases, this patient had HBV infection as the underlying disease. The cell of conventional ICC is usually small and its nucleus occupies a large part of the cell. Clear cell ICC consists of larger cells with copious cytoplasm possibly caused by mucin, lipid, glycogen or by another unknown reason. Therefore the cells look clear. The cancer cells originating from bile ducts often produce much mucin, however the clear cells in this case did not contain mucin, and had a little glycogen.

The literature review disclosed that the risk of metastasis or recurrence is low after the removal of the cancer. There is not enough evidence for the use of any particular treatment including chemotherapy. Therefore, careful follow-up and the acquisition of more case records are important to obtain more evidence on this cancer.


Story Source:

The above story is based on materials provided by World Journal of Gastroenterology. Note: Materials may be edited for content and length.


Journal Reference:

  1. Toriyama E, Nanashima A, Hayashi H, Abe K, Kinoshita N, Yuge S, Nagayasu T, Uetani M, Hayashi T. A case of intrahepatic clear cell cholangiocarcinoma. World Journal of Gastroenterology, 2010; 16 (20): 2571 DOI: 10.3748/wjg.v16.i20.2571

Cite This Page:

World Journal of Gastroenterology. "Intrahepatic clear cell cholangiocarcinoma." ScienceDaily. ScienceDaily, 2 June 2010. <www.sciencedaily.com/releases/2010/06/100602094509.htm>.
World Journal of Gastroenterology. (2010, June 2). Intrahepatic clear cell cholangiocarcinoma. ScienceDaily. Retrieved October 25, 2014 from www.sciencedaily.com/releases/2010/06/100602094509.htm
World Journal of Gastroenterology. "Intrahepatic clear cell cholangiocarcinoma." ScienceDaily. www.sciencedaily.com/releases/2010/06/100602094509.htm (accessed October 25, 2014).

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