Page 41 - WNS 2022 Exhibitors E-Program Booklet
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Spontaneous Resolution of Chiari I Malformation in an Adult. A Case
             Report and Literature Review
             Barbara Lazio, MD, FAANS, Providence-Swedish NeurosurgeryWestern
             Washington
             Co-authors: Dahlia Scher, BSc, University of California San Diego
             Introduction:
             With the wide availability of magnetic resonance imaging for brain and cervi-
             cal spine complaints, adult patients are diagnosed with Chiari I malformation
             more  frequently.    While  there  are  few  reports  of  spontaneous  resolution  of
             Chiari I malformation in adults, it is important to consider when choosing con-
             servative versus surgical management in minimally symptomatic and asymp-
             tomatic patients.
             Case Report:
             A woman presented to a neurosurgeon at age 55 with a two-year history of
             left-sided  headaches  and  left  facial  numbness.  She  had  no  association  of
             headache with position, cough, or Valsalva. MRI brain demonstrated cerebel-
             lar  tonsillar  ectopia  12  mm  below  the  foramen  magnum.      Due  to  atypical
             symptoms, surgical management was not recommended.  She presented ten
             years later with dizziness and gait disturbance.  MRI cervical spine showed
             resolution of cerebellar tonsillar ectopia and no syringomyelia.
             Methods:
             A comprehensive literature review was conducted on PubMed, Google Schol-
             ar and Web of Science with keywords “Chiari I malformation,” “spontaneous
             resolution,”  and  “adult.”   Articles including  exclusively  pediatric  patients  and
             patients  treated  surgically  were  excluded.    Articles  including  treatment  for
             other intracranial pathologies were excluded.
             Results and Conclusions:
             We identified sixteen cases of spontaneous regression of adult Chiari I mal-
             formation in the literature. The case presented was similar to the 16 previous-
             ly  reported cases  in the  nonoperative treatment.  Unlike  the  previous  cases,
             this  patient  never  had  symptoms  attributable  to  Chiari  I  malformation.    The
             natural history of minimally and asymptomatic Chiari I malformation in adults
             is  not  well  documented  radiographically.  This  case  illustrates  radiographic
             resolution  of  cerebellar  tonsillar  ectopia  and  strengthens  the  argument  for
             conservative  management  in  patients  with  radiographic  cerebellar  tonsillar
             ectopia and atypical symptoms.
             Figure  1.    A.  Sagittal  T1  brain  MRI  2011  demonstrating  12  mm  cerebellar
             tonsillar ectopia B. Sagittal T2 cervical spine MRI 2021 demonstrating resolu-
             tion of cerebellar tonsillar ectopia


            A                             B












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