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논문 기본 정보

자료유형
학술저널
저자정보
Jae Won Song (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Ho Soo Chun (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Jae Seung Lee (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Hye Won Lee (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Beom Kyung Kim (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Seung Up Kim (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Jun Yong Park (Department of Internal Medicine Institute of Gastroenterology Yonsei University College of Medicine) Sang Hoon Ahn (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine) Young Nyun Park (Department of Pathology Yonsei University College of Medicine) Dai Hoon Han (Department of Surgery Yonsei University College of Medicine) Do Young Kim (Department of Internal MedicineInstitute of Gastroenterology Yonsei University College of Medicine)
저널정보
대한간암학회 Journal of Liver Cancer Journal of Liver Cancer Vol.21 No.1
발행연도
2021.1
수록면
69 - 75 (7page)

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Hepatocellular carcinoma (HCC) primarily originates in the liver with hepatic differentiation. However, HCCs are not homogenous, and approximately 35% of HCC cases are classified as histopathological variants that present distinct pathologic characteristics. In particular, the lymphocyte-rich variant is the rarest subtype accounting for less than 1% of HCCs, which is not well known to date about molecular features and pathophysiology. Herein, we present a case of a patient who was suspected of metastatic liver cancer and confirmed as lymphocyterich HCC pathologically. A 78-year-old woman who underwent a right hemicolectomy for colon cancer was referred to our hospital for a newly detected liver mass. We could not make a decision because of insufficient evidence for diagnosis from imaging studies. After resection, we found that it was a lymphocyte-rich HCC. The pathologic features and prognostic trends of this subtype are also discussed.

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