Interactive Transcript
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This is a FLAIR image from an MR
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of the brain in an adolescent
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with tuberous sclerosis complex and seizures.
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We can see multifocal areas of cortical
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dysplasia throughout both
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cerebral hemispheres,
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we can see some of these have
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a cystic component.
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So these are classic findings of
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tuberous sclerosis complex. Now,
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it's important to note there are two different
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genes involved in the tuberous sclerosis complex.
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There's the TSC1 gene and the TSC2 gene,
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the TSC1 and TSC2 genes produce
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the proteins tuberin and,
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and hamartin which come
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together and together,
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they are a regulatory protein
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in the mTOR pathway.
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They suppress that pathway
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that mTOR pathway. So,
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if you have an abnormality in
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either tuberin or hamartin,
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that that dimer no longer will suppress the
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mTOR pathway and you will get unregulated
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action of that pathway or incompletely
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regulated action.
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That's one of the reasons why exogenous mTOR
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inhibitors can be used to treat some of the
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findings in tuberous sclerosis complex.
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In particular,
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the subependymal giant cell astrocytoma. Now,
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patients with defects in the TSC2 gene,
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often not always,
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often have more severe brain abnormalities
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and more severe and more difficult
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to control seizures. Now,
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one of the things that is an interesting and
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important association to be aware of even
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though it goes outside the brain is this.
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Now,
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we know that tuberous sclerosis complex is
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associated with cystic renal disease and
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associated with formation of renal angiomyolipoma.
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Those renal angiomyolipomas can hemorrhage when
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they get large. But these cysts here,
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this is more than just cystic renal
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disease of tuberous sclerosis complex.
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This is actually autosomal dominant
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polycystic kidney disease. Well,
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it turns out that the gene for autosomal
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dominant polycystic kidney disease is very
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closely located to the TSC2 gene.
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So this patient actually has dual disease due
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to the genetic proximity of the TSC2
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gene and the autosomal dominant polycystic
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kidney disease gene. So,
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right there from imaging,
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we pretty much can be certain that this
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patient has an abnormality of the TSC2 gene.
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Now,
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that's not something typically that you would
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need a radiologist to be able to make the
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diagnosis. There are genetic tests for that.
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But understanding that relationship and
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understanding that there are different gene
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subtypes of tuberous sclerosis complex and
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potentially different management is something
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that's helpful and important to convey
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to the referring physician,
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whether it be a neuro epilepsy, neurologist,
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whether it be a nephrologist,
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an oncologist that you understand what's going
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on with these patients and with
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this disease process.
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So this patient again has tuberous sclerosis
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complex related to TSC2 gene and also an
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abnormality resulting in autosomal
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dominant polycystic kidney disease.
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