Superior canal dehiscence syndrome

Source: Wikipedia, the free encyclopedia.
Superior canal dehiscence syndrome
Other namesSCDS
SpecialtyNeurotology, neurology, ENT

The semicircular canal dehiscence (SCD) is a category of rare

neurotological diseases/disorders affecting the inner ears, which gathers the superior SCD, lateral SCD and posterior SCD. These SCDs induce SCD syndromes (SCDSs), which define specific sets of hearing and balance symptoms.[1][2]
This entry mainly deals with the superior SCDS.

The superior semicircular canal dehiscence syndrome (SSCDS) is a set of hearing and balance symptoms that a rare disease/disorder of the

superior semicircular canal of the vestibular system. There is evidence that this rare defect, or susceptibility, is congenital.[6][7] There are also numerous cases of symptoms arising after physical trauma to the head. It was first described in 1998 by Lloyd B. Minor of Johns Hopkins University in Baltimore.[8]

Symptoms

The superior canal dehiscence can affect both hearing and balance to different extents in different people.[citation needed]

Symptoms of the SCDS include:

  • Autophony – person's own speech or other self-generated noises (e.g. heartbeat, eye movements, creaking joints, chewing) are heard unusually loudly in the affected ear
  • superior semicircular canal
  • Tullio phenomenon – sound-induced vertigo, disequilibrium or dizziness, nystagmus and oscillopsia
  • Pulse-synchronous oscillopsia
  • Hyperacusis – the over-sensitivity to sound
  • Low-frequency conductive hearing loss
  • A feeling of fullness in the affected ear
  • Brain fog
  • Fatigue
  • Headache/migraine
  • Tinnitus – high pitched ringing in the ear

Symptoms in detail

Causes

According to current research, in approximately 2.5% of the general population the bones of the head develop to only 60–70% of their normal thickness in the months following birth. This genetic predisposition may explain why the section of temporal bone separating the superior semicircular canal from the cranial cavity, normally 0.8 mm thick, shows a thickness of only 0.5 mm, making it more fragile and susceptible to damage through physical head trauma or from slow erosion. An explanation for this erosion of the bone has not yet been found.[citation needed]

Diagnosis

The presence of dehiscence can be detected by a high definition (0.6 mm or less) coronal

VNG), electrocochleography (ECOG) and the rotational chair test. An accurate diagnosis is of great significance as unnecessary exploratory middle ear surgery may thus be avoided. Several of the symptoms typical to SCDS (e.g. vertigo and Tullio) may also be present singly or as part of Ménière's disease, sometimes causing the one illness to be confused with the other. There are reported cases of patients being affected by both Ménière's disease and SCDS concurrently.[citation needed
]

As SCDS is a very rare and still a relatively unknown condition, obtaining an accurate diagnosis of this distressing (and even disabling) disease may take some time as many health care professionals are not yet aware of its existence and frequently dismiss symptoms as being mental health-related.[12]

Treatment

Once diagnosed, the gap in the temporal bone can be repaired by surgical resurfacing of the affected bone or plugging of the superior semicircular canal.[13][unreliable source?][14] These techniques are performed by accessing the site of the dehiscence either via a middle fossa craniotomy or via a canal drilled through the transmastoid bone behind the affected ear. Bone cement has been the material most often used, in spite of its tendency to slippage and resorption, and a consequent high failure rate; recently, soft tissue grafts have been substituted.[15]

Eponym

Occasionally this disorder has been referred to as Minor's syndrome, after its discoverer, Lloyd B. Minor. However, that eponym has also been given to an unrelated condition, the paralysis and anaesthesia following a spinal injury, which is named after the Russian neurologist, Lazar Minor (1855–1942). In the latter case this term is now nearly obsolete.[16]

Known cases

References

  1. PMID 21124219
    .
  2. .
  3. .
  4. .
  5. .
  6. ^ Murray, Melissa (March 8, 1999). "Old Bone Collection Reveals Basis for Some Dizziness". The Johns Hopkins Gazette. 28 (25).
  7. ^ Duffy, Jim (1999). "The Clue in the Old Bones". Hopkins Medical News. Archived from the original on 2016-06-05. Retrieved 2008-01-20.
  8. PMID 9525507
    .
  9. .
  10. ^ "Symptoms of Superior Canal Dehiscence Syndrome". Johns Hopkins Medicine. 16 October 2021.
  11. PMID 31920911
    .
  12. .
  13. ^ "superior semicircular canal dehiscence - superior canal dehiscence syndrome". www.otosurgery.org. Archived from the original on 2017-08-24. Retrieved 2008-01-20.
  14. ^ Kertesz, Thomas R; Shelton, Clough; Wiggins, Richard; Galstonbury, Christine; Layton, Bryan J.; Worthington, Don W.; Harnsberger, H. Ric (October 2001). "Superior semi-circular canal dehiscence: Resurfacing with calcium phosphate bone cement". Australian Journal of Otolaryngology. 4 (3): 167–173.
  15. S2CID 8313147
    .
  16. Who Named It?

External links