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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2023.3
- 수록면
- 219 - 224 (6page)
- DOI
- 10.17998/jlc.2023.02.24
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초록· 키워드
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Hepatoblastoma is an exceptionally rare malignancy in adults with just over 70 non-pediatriccases reported in literature. Recounted is a case of a 49-year-old female who presented withacute right upper quadrant abdominal pain, elevated serum alpha fetoprotein and a largeliver mass on imaging. Hepatectomy was performed under clinical suspicion of hepatocellularcarcinoma. Immunomorphologic characteristics of the tumor proved consistent withhepatoblastoma of mixed epithelial and mesenchymal type. Hepatocellular carcinomaremains to be the primary differential diagnosis for adult hepatoblastoma, however, distinguishing between these two neoplasms requires close histomorphologic assessment and immunohistochemical profiling as clinical, radiologic and gross pathologic findings typically overlap. Making this distinction is highly crucial in the timely initiation of surgical and chemotherapeutic interventions for this inherently aggressive and rapidly fatal disease.
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