Intracranial metastasis in fibrolamellar hepatocellular carcinoma

被引:6
|
作者
Hammond, William J. [1 ,2 ]
Lalazar, Gadi [2 ]
Saltsman, James A. [1 ,2 ]
Farber, Benjamin A. [1 ,2 ]
Danzer, Enrico [1 ]
Sherpa, Tshering C. [2 ]
Banda, Charles D. [2 ]
Andolina, Jeffrey R. [3 ]
Karimi, Sasan [4 ]
Brennan, Cameron W. [5 ,6 ]
Torbenson, Michael S. [7 ]
La Quaglia, Michael P. [1 ]
Simon, Sanford M. [2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Serv Pediat, 1275 York Ave, New York, NY 10065 USA
[2] Rockefeller Univ, Lab Cellular Biophys, New York, NY 10065 USA
[3] Univ Rochester, Med Ctr, Dept Pediat, Golisano Childrens Hosp, Rochester, NY 14642 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, New York, NY 10065 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Neurosurg, New York, NY 10065 USA
[7] Mayo Clin, Div Anat Pathol, Dept Pathol, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
adolescent and young adult tumors; brain; fibrolamellar; liver; rare tumors; tumors; tumor biology; LIVER; DNAJB1-PRKACA; DIAGNOSIS; PROGNOSIS; THERAPY; PATIENT; TUMORS;
D O I
10.1002/pbc.26919
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fibrolamellar hepatocellular carcinoma (FLHCC) is a rare liver malignancy in adolescents and young adults. Surgery is the mainstay of therapy for primary and metastatic disease. Most patients relapse, with development of both local and distant metastases. Brain metastases from solid tumors are rare in the pediatric and young adult population. Here, we document three patients with brain metastases from FLHCC, confirmed by histology and molecular characterization of the chimeric fusion DNAJB1-PRKACA, each necessitating neurosurgical intervention. These observations highlight the ability of FLHCC to metastasize to the brain and suggest the need for surveillance neuroimaging for patients with advanced-stage disease.
引用
收藏
页数:5
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