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Journal of the Korean Liver Cancer Study 2002;2(1):88-92.
Published online July 31, 2002.
5 Case Reports of Hepatic Epithelioid Hemangioendothelioma
Beom Jin Kim1, Moon Seok Choi1, Kwang Cheol Koh1, Seung Woon Paik1, Won Jae Lee2, Cheol Keun Park3
1Department of Internal Medicine, Sungkyunkwan University School of Medicine, Seoul, Korea
2Departments of Radiology, Sungkyunkwan University School of Medicine, Seoul, Korea
3Departments of Pathology, Sungkyunkwan University School of Medicine, Seoul, Korea
Correspondence:  Moon Seok Choi,
Email: hongy@unitel.co.kr
Copyright ©2002 by The Korean Liver Cancer Association
Abstract
Background/Aims: Hepatic epithelioid hemangioendothelioma is a rare vascular tumor of the liver. It poses special difficulties for clinicians in its diagnosis and treatment. Its clinical course and prognosis are variable. However, there are only a few case reports in Korea. Therefore we studied the clinical characteristics of hepatic epithelioid hemangioendothelioma which had been diagnosed and treated in our hospital. Methods: The clinical, radiological and pathologic characteristics of 5 cases were reviewed retrospectively. Results: The patients included three males and two females and the mean age was 48.6 years. The chief complaints were asymptomatic (4 cases) or abdominal pain (1 case). Blood chemistry test was abnormal in one patient. CT scan showed multiple hypoattenuated masses in the periphery of the liver. Ultrasound-guided liver biopsy was done for all cases. On the immunohistochemical staining, factor Ⅷ was positive in three cases, CD34 was positive in three cases. In the treatment, conservative management was done for all cases. There was no significant disease progression during the follow-up period of 25.4 months. Conclusions: Hepatic epithelioid hemangioendothelioma presents nonspecific symptoms and shows low grade malignancy and slow disease progression. Radiologic studies such as CT with biopsy may give the clue for the diagnosis.
Key Words: Hepatic epithelioid hemangioendothelioma; Factor Ⅷ; CD34
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