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Cranial nerve vascular compression syndromes of the trigeminal, facial and vago-glossopharyngeal nerves: comparative anatomical study of the central myelin portion and transitional zone; correlations with incidences of corresponding hyperactive dysfunctional syndromes

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Abstract

Objective

The aim of this study was to evaluate the anatomy of the central myelin portion and the central myelin-peripheral myelin transitional zone of the trigeminal, facial, glossopharyngeal and vagus nerves from fresh cadavers. The aim was also to investigate the relationship between the length and volume of the central myelin portion of these nerves with the incidences of the corresponding cranial dysfunctional syndromes caused by their compression to provide some more insights for a better understanding of mechanisms.

Methods

The trigeminal, facial, glossopharyngeal and vagus nerves from six fresh cadavers were examined. The length of these nerves from the brainstem to the foramen that they exit were measured. Longitudinal sections were stained and photographed to make measurements. The diameters of the nerves where they exit/enter from/to brainstem, the diameters where the transitional zone begins, the distances to the most distal part of transitional zone from brainstem and depths of the transitional zones were measured. Most importantly, the volume of the central myelin portion of the nerves was calculated. Correlation between length and volume of the central myelin portion of these nerves and the incidences of the corresponding hyperactive dysfunctional syndromes as reported in the literature were studied.

Results

The distance of the most distal part of the transitional zone from the brainstem was 4.19 ± 0.81 mm for the trigeminal nerve, 2.86 ± 1.19 mm for the facial nerve, 1.51 ± 0.39 mm for the glossopharyngeal nerve, and 1.63 ± 1.15 mm for the vagus nerve. The volume of central myelin portion was 24.54 ± 9.82 mm3 in trigeminal nerve; 4.43 ± 2.55 mm3 in facial nerve; 1.55 ± 1.08 mm3 in glossopharyngeal nerve; 2.56 ± 1.32 mm3 in vagus nerve.

Correlations (p < 0.001) have been found between the length or volume of central myelin portions of the trigeminal, facial, glossopharyngeal and vagus nerves and incidences of the corresponding diseases.

Conclusion

At present it is rather well-established that primary trigeminal neuralgia, hemifacial spasm and vago-glossopharyngeal neuralgia have as one of the main causes a vascular compression. The strong correlations found between the lengths and volumes of the central myelin portions of the nerves and the incidences of the corresponding diseases is a plea for the role played by this anatomical region in the mechanism of these diseases.

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References

  1. Auger RG (1990) Whisnant JP: hemifacial spasm in Rochester and Olmsted County, Minnesota, 1960 to 1984. Arch Neurol 47(11):1233–1234

    PubMed  CAS  Google Scholar 

  2. Burchiel KJ (1980) Abnormal impulse generation in focally demyelinated trigeminal roots. J Neurosurg 53(5):674–683

    Article  PubMed  CAS  Google Scholar 

  3. Chawla JC, Falconer MA (1967) Glossopharyngeal and vagal neuralgia. Br Med J 3(5564):529–531

    Google Scholar 

  4. Dandy WE (1934) Concerning the cause of trigeminal. Am J Surg 24:447–495

    Article  Google Scholar 

  5. De Ridder D, Møller A, Verlooy J, Cornelissen M, De Ridder L (2002) Is the root entry/exit zone important in microvascular compression syndromes? Neurosurgery 51(2):427–434

    PubMed  Google Scholar 

  6. Gardner WJ, Miklos MV (1959) Response of trigeminal neuralgia to decompression of sensory root; discussion of cause of trigeminal neuralgia. J Am Med Assoc 170(15):1773–1776

    PubMed  CAS  Google Scholar 

  7. Gardner WJ (1962) Concerning the mechanism of trigeminal neuralgia and hemifacial spasm. J Neurosurg 19:947–958

    Article  PubMed  CAS  Google Scholar 

  8. Guclu B, Meyronet D, Simon E, Streichenberger N, Sindou M, Mertens P (2009) Structural anatomy of cranial nerves (V, VII, VIII, IX, X). Neurochirurgie 55(2):92–98

    Article  PubMed  CAS  Google Scholar 

  9. Guevara N, Deveze A, Buza V, Laffont B, Magnan J (2008) Microvascular decompression of cochlear nerve for tinnitus incapacity: pre-surgical data, surgical analyses and long-term follow-up of 15 patients. Eur Arch Otorhinolaryngol 265(4):397–401

    Article  PubMed  Google Scholar 

  10. Jannetta PJ (1967) Arterial compression of the trigeminal nerve at the pons in patients with trigeminal neuralgia. J Neurosurg 26(1):Suppl:159–162

    Google Scholar 

  11. Jannetta PJ (1975) Neurovascular cross-compression in patients with hyperactive dysfunction symptoms of the eighth cranial nerve. Surg Forum 26:467–469

    PubMed  CAS  Google Scholar 

  12. Jannetta PJ (1979) Microsurgery of cranial nerve cross-compression. Clin Neurosurg 26:607–615

    PubMed  CAS  Google Scholar 

  13. Jannetta PJ, Møller MB, Møller AR (1984) Disabling positional vertigo. N Engl J Med 310(26):1700–1705

    Google Scholar 

  14. Katusic S, Beard CM, Bergstralh E, Kurland LT (1990) Incidence and clinical features of trigeminal neuralgia, Rochester, Minnesota, 1945–1984. Ann Neurol 27(1):89–95

    Article  PubMed  CAS  Google Scholar 

  15. Laha RK, Jannetta PJ (1977) Glossopharyngeal neuralgia. J Neurosurg 47(3):316–320

    Article  PubMed  CAS  Google Scholar 

  16. Kommerell G, Mehdorn E, Ketelsen UP (1985) Oculomotor paralysis with cyclic spasms; electromyographic and electron microscopic indications of chronic peripheral nerve irritation. Fortschr Ophthalmol 82(2):203–204

    PubMed  CAS  Google Scholar 

  17. Mikami T, Minamida Y, Ohtsuka K, Houkin K (2005) Resolution of superior oblique myokymia following microvascular decompression of trochlear nerve. Acta Neurochir (Wien) 147(9):1005–1006

    Article  CAS  Google Scholar 

  18. Møller AR (1999) Vascular compression of cranial nerves: II: pathophysiology. Neurol Res 21(5):439–443

    PubMed  Google Scholar 

  19. Møller MB, Møller AR, Jannetta PJ, Jho HD (1993) Vascular decompression surgery for severe tinnitus: selection criteria and results. Laryngoscope 103(4 Pt 1):421–417

    Article  PubMed  Google Scholar 

  20. Møller MB, Møller AR, Jannetta PJ, Jho HD, Sekhar LN (1993) Microvascular decompression of the eighth nerve in patients with disabling positional vertigo: selection criteria and operative results in 207 patients. Acta Neurochir (Wien) 125(1–4):75–82

    Article  Google Scholar 

  21. Obersteiner H, Redlich E (1984) Uber Wesen und Pathogenese der Tabischen Hinterstrangsdegeneration. Arb Neurol Inst Wien Univ 1–3:158–172

    Google Scholar 

  22. Patel A, Kassam A, Horowitz M, Chang YF (2002) Microvascular decompression in the management of glossopharyngeal neuralgia:analysis of 217 cases. Neurosurgery 50(4):705–711

    Article  PubMed  Google Scholar 

  23. Peker S, Kurtkaya O, Uzün I, Pamir MN (2006) Microanatomy of the central myelin-peripheral myelin transition zone of the trigeminal nerve. Neurosurgery 59(2):354–359

    Article  PubMed  Google Scholar 

  24. Ryu H, Yamamoto S, Sugiyama K, Nozue M (1998) Neurovascular compression syndrome of the eighth cranial nerve. What are the most reliable diagnostic signs? Acta Neurochir (Wien) 140(12):1279–1286

    Article  CAS  Google Scholar 

  25. Sakas DE, Panourias IG, Stranjalis G, Stefanatou MP, Maratheftis N, Bontozoglou N (2007) Paroxysmal otalgia due to compression of the intermediate nerve: a distinct syndrome of neurovascular conflict confirmed by neuroimaging. Case report. J Neurosurg 107(6):1228–1230

    Article  PubMed  Google Scholar 

  26. Samii M, Rosahl SK, Carvalho GA, Krzizok T (1998) Microvascular decompression for superior oblique myokymia: first experience. Case report. J Neurosurg 89(6):1020–1024

    Article  PubMed  CAS  Google Scholar 

  27. Scharwey K, Krzizok T, Samii M, Rosahl SK, Kaufmann H (2000) Remission of superior oblique myokymia after microvascular decompression. Ophthalmologica 214(6):426–428

    Article  PubMed  CAS  Google Scholar 

  28. Sindou M, Quoex C, Baleydier C (1974) Fiber organization at the posterior spinal cord-rootlet junction in man. J Comp Neurol 153(1):15–26

    Article  PubMed  CAS  Google Scholar 

  29. Sindou M, Henry JF, Blanchard P (1991) Idiopathic neuralgia of the glossopharyngeal nerve. Study of a series of 14 cases and review of the literature. Neurochirurgie 37(1):18–25

    PubMed  CAS  Google Scholar 

  30. Sindou M, Chiha M, Mertens P (1995) Anatomical findings in microsurgical vascular decompression for trigeminal neuralgia. Correlations between topography of pain and site of the neuro-vascular conflict. Acta Neurochir Suppl 64:125–127

    PubMed  CAS  Google Scholar 

  31. Sindou M, Howeidy T, Acevedo G (2002) Anatomical observations during microvascular decompression for idiopathic trigeminal neuralgia (with correlations between topography of pain and site of the neurovascular conflict). Prospective study in a series of 579 patients. Acta Neurochir (Wien) 144(1):1–13

    Article  CAS  Google Scholar 

  32. Sindou MP (2005) Microvascular decompression for primary hemifacial spasm. Importance of intraoperative neurophysiological monitoring. Acta Neurochir (Wien) 147(10):1019–1026

    Article  CAS  Google Scholar 

  33. Sindou M, Leston J, Decullier E, Chapuis F (2007) Microvascular decompression for primary trigeminal neuralgia: long-term effectiveness and prognostic factors in a series of 362 consecutive patients with clear-cut neurovascular conflicts who underwent pure decompression. J Neurosurg 107(6):1144–1153

    Article  PubMed  Google Scholar 

  34. Sindou M, Leston JM, Decullier E, Chapuis F (2008) Microvascular decompression for trigeminal neuralgia: the importance of a noncompressive technique—Kaplan-Meier analysis in a consecutive series of 330 patients. Neurosurgery 63(4 Suppl 2):341–351

    Article  PubMed  Google Scholar 

  35. Sindou M, Keravel Y (2009) Neurosurgical treatment of vago-glossopharyngeal neuralgia. Neurochirurgie 55(2):231–235

    Article  PubMed  CAS  Google Scholar 

  36. Sindou M, Keravel Y (2009) Functional neurosurgery in the cranial nerve hyperactivity syndromes. Neurochirurgie 55(2):75–291

    Article  PubMed  CAS  Google Scholar 

  37. Sindou M, Keravel Y (2009) Neurosurgical treatment of primary hemifacial spasm with microvascular decompression. Neurochirurgie 55(2):236–247

    Article  PubMed  CAS  Google Scholar 

  38. Skinner HA (1931) Some histological features of the cranial nerves. Arch Neurol Psychiatry 25:356–372

    Google Scholar 

  39. Słoniewski P, Korejwo G, Zieliński P, Moryś J, Krzyzanowski M (1999) Measurements of the Obersteiner-Redlich zone of the vagus nerve and their possible clinical applications. Folia Morphol (Warsz) 58(1):37–41

    Google Scholar 

  40. Spurling RG, Grantham EG (1942) Glossopharyngeal neuralgia. South Med J 35:509–512

    Article  Google Scholar 

  41. Tarlov IM (1937) Structure of the nerve root. I. Nature of the junction between the central and the peripheral nervous system. Archs Neurol Psychiat 37:555–583

    Google Scholar 

  42. Tarlov IM (1937) Structure of the nerve root. II. Differentiation of sensory from motor roots; observations on identification of function in roots of mixed cranial nerves. Arch Neurol Psychiatry 37:1338–1355

    Google Scholar 

  43. Tomii M, Onoue H, Yasue M, Tokudome S, Abe T (2003) Microscopic measurement of the facial nerve root exit zone from central glial myelin to peripheral Schwann cell myelin. J Neurosurg 99(1):121–124

    PubMed  Google Scholar 

  44. Vasama JP, Moller MB, Moller AR (1998) Microvascular decompression of the cochlear nerve in patients with severe tinnitus. Preoperative findings and operativeoutcome in 22 patients. Neurol Res 20(3):242–248

    PubMed  CAS  Google Scholar 

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Correspondence to Bulent Guclu.

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Guclu, B., Sindou, M., Meyronet, D. et al. Cranial nerve vascular compression syndromes of the trigeminal, facial and vago-glossopharyngeal nerves: comparative anatomical study of the central myelin portion and transitional zone; correlations with incidences of corresponding hyperactive dysfunctional syndromes. Acta Neurochir 153, 2365–2375 (2011). https://doi.org/10.1007/s00701-011-1168-1

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