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Genomic Spine
Disease
Case Presentations |
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Disc Herniation Producing Cauda Equina Compression
in a 15 year old girl
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Shown above are some remarkable MRI scans of a 15 year old female high
school student showing classic evidence of JDD and associated degenerative
changes. A large disc herniation at L4-5 level has produced marked
compression of the nerve roots of the cauda equina, as shown on the right.
This student's mother also had JDD and unsuccessful spine surgery earlier
in her life. At the time of decompressive surgery on this patient
segmental instability was documented at the L4-5 level and restorative
spine surgery using a single posterior titanium cage and dorso-lateral
strut stabilization was carried out. |
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Disc Herniation Producing Complete Foot Drop and Bladder Impairment
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R. M. is a 48 year old police chief with back pain over 20 years due to
a genomic spine condition. He underwent discectomy in 1977 and in
February 2002 developed complete foot drop on the right associated with
bladder problems. At the time of this discectomy a dorso-lateral
strut was placed from L3 to the sacrum to address multi-level segmental
instability. A 3-D reconstruction CT image performed 1½
years following surgery is shown. Patient experienced complete
recovery of motor and sensory function and for the first time in many
decades was free of back and leg pain (see questionnaire). This is
an example where restorative surgical techniques were employed to provide
long-lasting, more physiologic, and effective results for a genomic
condition. |
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D.K. is a 50 year old whose multi-level genomic disease process was finally
documented in 2003. Like many patients with genomic problems D.K. experienced
herniated lumbar discs for which he had surgery in 1984 and 1986.
Because of continuing back pain he was seen by a scoliosis/deformity spine
specialist who performed a rigid 3 level pedicle
screw instrumented posterior and an interbody fusion
in 1996. Patient's pain and disability were not improved and he was
referred to a Pain Management Clinic where a morphine pump was implanted in
year 2000. Because the intrathecal catheter caused thoracic adhesive
arachnoiditis producing catheter obstruction the morphine pump and catheter
had to be removed. D.K. remains incapacitated and continues to take strong narcotic
medications to help him make it through the day.
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The case presented above is true. Unfortunately, this story is not a
unique one. The on-going failure to properly diagnose and
appropriately treat multi-level degenerative problems associated with
genomic conditions, are responsible for many similar treatment disasters.
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