Glioblastoma multiforme in a child with tuberous sclerosis complex

被引:15
|
作者
Vignoli, Aglaia [1 ]
Lesma, Elena [2 ]
Alfano, Rosa Maria [3 ]
Peron, Angela [1 ]
Scornavacca, Giulia Federica [1 ]
Massimino, Maura [4 ]
Schiavello, Elisabetta [4 ]
Ancona, Silvia [2 ]
Cerati, Michele [5 ]
Bulfamante, Gaetano [3 ]
Gorio, Alfredo [2 ]
Canevini, Maria Paola [1 ]
机构
[1] Univ Milan, Dept Hlth Sci, San Paolo Hosp, Child Neurol Unit Epilepsy Ctr, I-20142 Milan, Italy
[2] Univ Milan, Dept Hlth Sci, Labs Pharmacol, Milan, Italy
[3] San Paolo Hosp, Dept Hlth Sci, Dept Human Pathol Cytogenet & Mol Pathol, Milan, Italy
[4] Ist Nazl Tumori, Fdn IRCCS, Dept Hematol & Pediat Oncoematol, Pediat Unit, I-20133 Milan, Italy
[5] Osped Circolo Varese, Dept Pathol, Varese, Italy
关键词
children; follow-up MR; Glioblastoma multiforme; Tuberous Sclerosis Complex; TSC; tumors; GRADE GLIOMA; CELLS; TSC1; ANGIOMYOLIPOMA; RADIOTHERAPY; BIOLOGY; TISSUES; GROWTH; TUMORS; GENE;
D O I
10.1002/ajmg.a.37158
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tuberous Sclerosis Complex (TSC) is characterized by the presence of benign tumors in the brain, kidneys, heart, eyes, lungs, and skin. The typical brain lesions are cortical tubers, subependimal nodules and subependymal giant-cell astrocytomas. The occurrence of malignant astrocytomas such as glioblastoma is rare. We report on a child with a clinical diagnosis of TSC and a rapidly evolving glioblastoma multiforme. Genetic analysis identified a de novo mutation in TSC2. Molecular characterization of the tumor was performed and discussed, as well as a review of the literature where cases of TSC and glioblastoma multiforme are described. Although the co-occurrence of TSC and glioblastoma multiforme seems to be rare, this possible association should be kept in mind, and proper clinical and radiological follow up should be recommended in these patients. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:2388 / 2393
页数:6
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