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Lost or fragmented bony septum of the optic canal facing the sphenoid sinus: a histological study using elderly donated cadavers

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Abstract

Purpose

To histologically describe a direct contact (the so-called dehiscence) of the optic nerve (ON) and/or internal carotid artery (ICA) to the mucosa of posterior paranasal sinuses represented by the sphenoid sinus (SS).

Methods

Observations of histological sections of unilateral or bilateral skull bases (parasellar area and orbital apex) from 22 elderly cadavers were made.

Results

A bony septum was less than 300 µm between the SS and ICA and 200 µm between the SS and optic nerve. Parts of the septa were sometimes absent due to fragmentation and holes of the bony lamella (2/22 facing the ICA; 4 facing the ICA in combination with an absent bony septum facing the nerve). In these dehiscence sites, the SS submucosal tissue attached to a thick sheath (50–100 µm in thickness) enclosing the optic nerve and ophthalmic artery and/or the ICA adventitia (50–200 µm in thickness). The ICA sometimes contained a sclerotic plaque that attached to or even protruded into the SS. With or without dehiscence, the SS mucosa was always thin (50–100 µm in thickness) and accompanied no mononuclear cellular infiltration or tumor.

Conclusions

A thin bony septum of the optic nerve or ICA had been notable as a danger point during surgery, but even a 0.05-mm-thick bone lamella might be an effective barrier against cellular infiltration or bacterial invasion from the SS. Fragmentation and holes of the bony lamella in 4 cadavers might allow cellular invasion to the optic nerve. Accordingly, unknown immunological cross talks might occur to cause demyelination.

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References

  1. Akdemir G, Tekdemir I, Altin L (2004) Transethmoidal approach to the optic canal: surgical and radiological microanatomy. Surg Neurol 62:268–274

    Article  Google Scholar 

  2. Ali IK, Sansare K, Karjodkar F et al (2020) Imaging analysis of Onodi cells on cone-beam computed tomography. Int Arch Otorhinolaryngol 24:e319–e322

    Article  Google Scholar 

  3. da Silva APB, Silva RBM, Goi LD et al (2020) Experimental models of neuroimmunological disorders: a review. Front Neurol 11:389

    Article  Google Scholar 

  4. Degaga T, Zenebe AM, Wirtu AT et al (2020) Anatomographic variants of sphenoid sinus in Ethiopian population. Diagnostics 10:970

    Article  Google Scholar 

  5. DeLano M, Fun F, Zinreich S (1996) Relationship of the optic nerve to the posterior paranasal sinuses: a CT anatomic study. Am J Neuroradiol 122:293–294

    Google Scholar 

  6. Duan T, Verkman AS (2020) Experimental animal models of aquaporin-4-IgG seropositive neuromyelitis optica spectrum disorders: progress and shortcomings. Brain Pathol 30:13–25

    Article  Google Scholar 

  7. Fujii K, Chambers SM, Rhoton AL (1979) Neurovascular relationships of the sphenoid sinus. J Neurosurg 50:31–39

    Article  CAS  Google Scholar 

  8. Gagliardi F, Donofrio CA, Spina A et al (2016) Endoscope-assisted transmaxillosphenoidal approach to the sellar and parasellar regions: an anatomic study. World Neurosurg 95:246–252

    Article  Google Scholar 

  9. Gay D, Dick G, Upton G (1979) Multiple sclerosis associated with sinusitis: case-controlled study in general practice. Lancet 8485:815–819

    Google Scholar 

  10. Graber DJ, Levy M, Kerr D et al (2008) Neuromyelitis optica pathogenesis and aquaporin 4. J Neuroinflammation 5:22

    Article  Google Scholar 

  11. Hosemann W, Draf C (2013) Danger points, complications and medio-legal aspects in endoscopic sinus surgery. GMS Curr Top Otorhinolaryngol Head Neck Surg. https://doi.org/10.3205/cto000098

    Article  PubMed  PubMed Central  Google Scholar 

  12. Itagi RM, Adiga CP, Kalenahalli K et al (2017) Optic nerve canal relation to posterior paranasal sinuses in Indian ethnics: review and objectice classification. J Clin Diagn Res 11:TC01–TC03

    PubMed  PubMed Central  Google Scholar 

  13. Johnson DW, Hopkins RJ, Hanafee WN et al (1985) The unprotected parasphenoidal carotid artery studies by high-resolution computed tomography. Radiology 155:137–141

    Article  CAS  Google Scholar 

  14. Kainz J, Stammberger H (1991) Gefahrenpunkte der hinteren Rhinobasis: Anatomische, histologische und endoskopische Befunde. Laryngorhinootologie 70:479–486

    Article  CAS  Google Scholar 

  15. Kennedy DW, Zinreich SJ, Hassab MH (1990) The internal carotid artery as it relates to endonasal sphenoethmoidectomy. Am J Rhinol 4:7–12

    Article  Google Scholar 

  16. Lang S, Michael Brainin, Neuhold A et al (1991) Multiple sclerosis associated with sinusitis: a case-controlled MRI study. Proceedings of the XIV symposium neuroradiologicum. pp 121–122

  17. Lennon VA, Kryzer TJ, Pittock SJ et al (2005) IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel. J Exp Med 202:473–477

    Article  CAS  Google Scholar 

  18. Locatelli M, Di Cristofori A, Draghi R et al (1991) Multiple sclerosis associated with sinusitis: a case-controlled MRI study. In: du Boulay G, Molyneux A, Moseley I (eds) Proceedings of the XIV symposium neuroradiologicum. Springer, Berlin.

  19. Lu Y, Pan J, Qi S, Shi J et al (2011) Pneumatization of the sphenoid sinus in Chinese: the differences from Caucasian and its application in the extended transsphenoidal approach. J Anat 219:132–142

    Article  Google Scholar 

  20. Ozturan O, Yenigun A, Degirmeci N et al (2013) Co-existence of the Onodi cell with the variation of perisphenoidal structures. Eur Arch Otorhinolaryngol 270:2057–2063

    Article  Google Scholar 

  21. Pandit L, Cox LM, Malli C et al (2021) Clostridium bolteae elevated in neuromyelitis optica spectrum disorder in India and shares sequence similarity with AQP4. Neurol Neuroimmunol Neuroinflamm 8:e907

    Article  Google Scholar 

  22. Papadopoulos MC, Bennett JL, Verkman AS (2014) Treatment of neuromyelitis optica: state-of-the-art and emerging therapies. Nat Rev Neurol 10:493–506

    Article  CAS  Google Scholar 

  23. Papadopoulos MC, Verkman AS (2012) Aquaporin 4 and neuromyelitis optica. Lancet Neurol 11:535–544

    Article  CAS  Google Scholar 

  24. Rahmati A, Ghafari R, AnjomShoa M (2016) Normal variations of sphenoid sinus and the adjacent structures detected in cone beam computed tomography. J Dent 17:32–37

    Google Scholar 

  25. Ratelade J, Verkman AS (2012) Neuromyelitis optica: aquaporin-4 based pathogenesis mechanisms and new therapies. Int J Biochem Cell Biol 44:1519–1530

    Article  CAS  Google Scholar 

  26. Ren Z, Wang Y, Duan T et al (2012) Cross-immunoreactivity between bacterial aquaporin-Z and human aquaporin-4: potential relevance to neuromyelitis optica. J Immunol 189:4602–4611

    Article  CAS  Google Scholar 

  27. Srikajon J, Siritho S, Ngamsombat C et al (2018) Differences in clinical features between optic neuritis in neuromyelitis optica spectrum disorders and in multiple sclerosis. Mult Scler J 4:1–12

    Google Scholar 

  28. Suzuki H, Oku H, Horie T et al (2014) Changes in expression of aquaporin-4 and aquaporin-9 in optic nerve after crushing in rats. PLoS One 9:e114694

    Article  Google Scholar 

  29. Winter A, Chwalisz B (2020) MRI characteristics of NMO, MOG and MS related optic neuritis. Semin Ophthalmol 35:333–342

    Article  Google Scholar 

  30. Zhang H, Liu X, Cheng Y et al (2013) A new method of locating the optic canal based on structures in sella region: computed tomography study. J Craniofac Surg 24:1011–1015

    Article  Google Scholar 

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Acknowledgements

The authors wish to sincerely thank those who donated their bodies to science so that anatomical research could be performed. Results from such research can potentially improve patient care and increase overall knowledge for the benefit of all mankind. These donors and their families deserve and have our highest gratitude. This work was supported by JSPS KAKENHI grants (Grant numbers: no. JP20K09895 [S.A.], and JP20K10191 [M.Y.]) and by the Tokyo Dental College Research Branding project.

Funding

This work was supported by JSPS KAKENHI grants (Grant numbers: JP20K09895 [S.A.] and JP20K10191 ([M.Y.]) and by the Tokyo Dental College Research Branding Project.

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Contributions

GM designed the study. KHC, TM, JS, JI, KH performed the experiments. MY, KK analysed the results. MY, GM, and SA prepared the manuscript.

Corresponding author

Correspondence to Kwang Ho Cho.

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Cho, K.H., Machida, T., Yamamoto, M. et al. Lost or fragmented bony septum of the optic canal facing the sphenoid sinus: a histological study using elderly donated cadavers. Surg Radiol Anat 44, 511–519 (2022). https://doi.org/10.1007/s00276-022-02910-1

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  • DOI: https://doi.org/10.1007/s00276-022-02910-1

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