Interactive Transcript
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We have just reviewed a variety
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of cases of patients with the different manifestations
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of neurofibromatosis type 1.
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This is a good reminder that
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neurofibromatosis type 1 is a single disease entity,
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but every single patient is different.
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Every single patient's clinical
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course is different.
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They get different manifestations of NF 1.
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Hopefully, at some point,
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we'll understand more about the genetics of it
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to figure out what manifestations
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different patients will get.
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Some patients get optic pathway gliomas.
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Some patients get intracranial neoplasms.
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Some patients get moyamoya vasculopathy.
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Some patients get plexiform neurofibromas,
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and they get combinations therein.
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These findings may not be present at first.
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They may develop over time.
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They may develop slowly,
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incrementally over the course of multiple studies.
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They may develop after just years and years
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of quiescence and then growth.
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We don't know.
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We can't predict it yet.
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It's important to do detailed follow
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up examinations on these patients,
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to look closely at the prior studies,
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not just the most recent prior study,
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but older prior studies.
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And it's important to recognize that
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the clinical pathway and decisions,
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a lot of times will depend upon what we find.
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So, be in communication with the referring doctors.
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And also, in terms of the imaging surveillance,
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sometimes it's performed every year,
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sometimes every two years.
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Sometimes it's just a brain.
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Sometimes it's a brain in orbits.
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It may involve a spine.
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Reach out to your pediatrician,
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your geneticists that are helping
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manage these patients,
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and figure out what is the most appropriate
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for that given patient.
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Some of these guidelines change over time,
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and they're changing as we speak.
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But
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what we need to do is just be a part of the
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team helping take care of these patients,
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and hopefully,
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we can be a valuable part of
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helping management.
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