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Are disc bulges or central disc
herniations clinically significant findings when revealed on
anatomical studies such as MRI or CT scanning, when there is
clinical correlation on physical examination? While this is a
controversy in some circles, clearly the scientific literature
supports that central/paracentral disc herniation or bulge without
neural impingement as significant when there is clinical correlation.
Recent studies with CT/discography have shown that there is an
entity of internal disc disruption that can cause the patient
pain prior to disc protrusion that may be evident on MRI or CT
scans.1,2,3 Bogduk has published similar work where he describes
"internal disc disruption" based on CT discography
studies.4 CT discography is an invasive diagnostic test whereby
dye is injected into the nucleus of a disc and subsequent CT
scans are obtained to see if and where there are leaks and whether
or not there is pain-provocation and reproduction of symptoms.
These studies show that not only
can disc herniation or bulge cause pain without nerve root compression,
but there can be internal disc disruption of the annulus with
apparent MR/CT changes that can cause pain. The annulus of the
disc has been shown by Bogduk and others to be well innervated
with both sensory and autonomic/sympathetic fibers of the sinuvertebral
nerve.5,6 There are mechanoreceptors, nociceptors, and chemoreceptors
that can detect all types of mechanical and biomechanical changes
occurring in the periphery of the disc. So a bulge or herniation
can cause c-nocipection by mechanical distension or the disc
and irritation of the sinuvertebral nerve branches that have
been demonstrated in the periphery of the annulus to a one-third
depth.
Other studies by researchers
have shown that chemicals and enzymes are present with disc protrusion
(phospholipise A, bradykinin, stromeolysn, histamine, VIP, and
substance P) that all can cause a patient to have pain by chemoreceptors.7
So disc herniation or bulge can cause a release of vasoactive
substances that cause pain. This must be present because studies
by Wiesel and others have shown that up to 30 percent of patients
that are asymptomatic will have MRI or CT changes consistent
with herniation, indicating it is an inactive disc protrusion
since the patient is asymptomatic.8 A research study by Olmarker
et al., showed that when they injected autologous nucleous pulpusis
material into the spinal canal of rabbits, nerve conduction latency
delays were noted to occur. This suggests that a herniated disc
can cause electrodiagnostic changes despite no nerve root compression.9
Another study by Jinkins et al.,
published their findings on 250 patients with disc herniation
without nerve root compromise. They found referred pain zones
in the back and extremities that were not dermatomal but were
actually autonomic referred pain zones due to irritation of the
sympathetic nerves of the sinuvertebral nerve.10 Again this study
shows that nerve root compression is not always necessary for
the disc to be considered active and pain producing.
In a single blinded study I published
in Manual Medicine,11 a group of patients with MRI documented
disc herniations and bulges were correlated with infra-red thermography.
The infra-red thermography scans showed good sensitivity for
documenting nerve irritation in the lower extremity. Since CT,
discography, MRI are anatomical tests, clinical correlation and
neurophysiologic tests are needed to determine the definitive
diagnosis and treatment approach. CT discography is highly invasive
and is not done on a regular basis. Neurophysiologic tests that
can be used include NCV, EMG, SSEP, and thermography. Infra-red
thermography is not painful, risk free, noninvasive, and can
help identify if a disc bulge or herniation is an active one.
Infra-red thermography can pick up somatosympathetic nociception
and activation due to innervation of the annulus by the sinuvertebral
nerve.
Another test which may be useful
is SSEP and DSSEP. Studies are beginning to be published on the
utility of segmental and dermatomal evoked potentials since these
techniques measure sensory dysfunction. A recent study by Green
et al., found that infra-red thermography has a high sensitivity
and specificity when compared to SEP/CT/EMG and NCV.12
- References
- 1.Ninomuya M: Pathoanatomy of
lumbar disc herniation as demonstrated by CT-discography. Spine,
17(11):1316, 1992.
- 2.Burki G: MRI signal patterns
of lumbar discs with low back pain. Spine, 17(2):1199, 1992.
- 3.Bernard TN: Lumbar discography
followed by CT. Spine 15(7):690, p.690, 1990.
- 4.Bogduk N: Pathology of lumbar
disc pain. Manual Medicine, 5:72-70, 1990.
- 5.Bogduk N: Innervation of the
cervical disc. Spine 11:873-878, 1988.
- 6.Yamashita T: Mechanosensitive
afferent units in the lumbar disc and adjacent muscle. Spine,
18(15):2252, 1993.
- 7.Saal JS, Franson RC: High
levels of inflammatory phospholipase A in lumbar disc herniation.
Spine, 15(7):674-678, 1990.
- 8.Weisel S: A study of CT incidence
of positive CAT scans in an asymptomatic group of patients. Spine
(9):549-551, 1984.
- 9.Olmarker K, Rydevik B: Autologous
nucleus pulposis induces neurophysiologic changes in procine
cauda equina nerve roots. Spine, 18(11):1425-1432, 1993.
- 10.Jinkins JR, Whittemore AR:
Anatomic basis of vertebrogenic pain and the autonomic syndrome
associated with lumbar disc extrusion. Am J of Radiology, 152:1277-1289,
June 1989.
- 11.BenEliyahu DJ, Silber BA:
Infra-red thermographic imaging of lumbar dysautonomia. Manual
Medicine, 6:130-135, 1991.
- 12.Green J et al. Efficacy of
neurodiagnostic studies. Pain Digest 2:213-217, 1992.
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