Metachronous Type I pleuropulmonary blastoma and atypical choroid plexus papilloma in a young child

被引:4
|
作者
Liu, David J. [1 ]
Perrier, Renee [2 ,6 ]
Wei, Xing-Chang [3 ]
Joseph, Jeffrey T. [4 ]
Strother, Douglas [5 ,6 ]
机构
[1] Univ Alberta, Fac Med & Dent, MD Program, Edmonton, AB, Canada
[2] Univ Calgary, Dept Med Genet, Cumming Sch Med, Calgary, AB, Canada
[3] Univ Calgary, Dept Radiol, Cumming Sch Med, Calgary, AB, Canada
[4] Univ Calgary, Dept Pathol, Cumming Sch Med, Calgary, AB, Canada
[5] Univ Calgary, Dept Oncol, Cumming Sch Med, Calgary, AB, Canada
[6] Univ Calgary, Dept Pediat, Cumming Sch Med, Calgary, AB, Canada
关键词
atypical choroid plexus papilloma; brain tumor; pleuropulmonary blastoma; DICER1;
D O I
10.1002/pbc.26160
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pleuropulmonary blastoma (PPB) is a rare childhood tumor, often associated with germline DICER1 mutations and a risk for development of other benign and malignant tumors, a constellation termed DICER1 syndrome. A 1-year-old male was diagnosed with Type I PPB and screened regularly thereafter for detection of intrathoracic and intraabdominal disease. Ten months after diagnosis of PPB, he presented with headaches and vomiting. He was diagnosed with atypical choroid plexus papilloma, a lesion not previously reported with PPB. The presence of central nervous system symptoms in patients with PPB or a phenotype suggestive of DICER1 syndrome should prompt early intracranial imaging.
引用
收藏
页码:2240 / 2242
页数:3
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