Azriel Amit, Gogos Andrew, Rogers TeWhiti, Moscovici Samuel, Lo Patrick, Drummond Katharine
Department of Neurosurgery, The Royal Melbourne Hospital, Parkville, Victoria, Australia; Department of Surgery, The University of Melbourne, Parkville, Victoria, Australia.
Department of Neurosurgery, The Royal Melbourne Hospital, Parkville, Victoria, Australia; Department of Surgery, The University of Melbourne, Parkville, Victoria, Australia.
J Clin Neurosci. 2019 Feb;60:153-155. doi: 10.1016/j.jocn.2018.10.083. Epub 2018 Oct 24.
Tuberous sclerosis complex (TSC) is a multisystem, autosomal dominant disorder with a wide clinical spectrum. The most common brain tumor associated with TSC is the low grade subependymal giant cell astrocytoma. Reports of high grade primary brain tumors in patients with TSC are rare. TSC1/2 mutation has been identified in glioblastoma (GBM) even though it probably does not increase the overall risk for GBM in patients with TSC. We present a 58-year-old patient with known TSC, admitted for new neurological symptoms, diagnosed with a large heterogeneous tumor involving most of the corpus callosum. Stereotactic needle brain biopsy confirmed the diagnosis to be GBM. Five previously reported similar cases are reviewed, reflecting diversity in clinical and radiological findings and indicating that a high index of clinical suspicion must be maintained in patients with TSC.
结节性硬化症(TSC)是一种多系统常染色体显性疾病,临床谱广泛。与TSC相关的最常见脑肿瘤是低级别室管膜下巨细胞星形细胞瘤。TSC患者发生高级别原发性脑肿瘤的报道很少。尽管TSC1/2突变可能不会增加TSC患者发生胶质母细胞瘤(GBM)的总体风险,但在胶质母细胞瘤中已发现该突变。我们报告一名58岁已知患有TSC的患者,因出现新的神经系统症状入院,诊断为累及大部分胼胝体的大型异质性肿瘤。立体定向针吸脑活检确诊为GBM。我们回顾了之前报道的5例类似病例,反映了临床和影像学表现的多样性,并表明对TSC患者必须保持高度的临床怀疑。