Skip to main content

Advertisement

Log in

White-matter commissures: a clinically focused anatomical review

  • Review
  • Published:
Surgical and Radiologic Anatomy Aims and scope Submit manuscript

Abstract

Purpose

The objective of this review is to provide a structured approach to the main white matter commissures, their anatomic and radiological definition and disease implications.

Methods

The Pubmed database and The JAMA Network were used for the literature review and the following terms were searched using Sort by: Best Match and Sort by: Most Recent: telencephalic commissure, forebrain commissure anatomy, fornix anatomy, commissure of fornix, posterior commissure, corpus callosum, commissural agenesis, Probst bundle, corpus callosum disorders review, corpus callosum diseases review, Marchiafava–Bignami, Alzheimer’s disease and Forel commissure; 36 papers were selected, one excluded due to the language barrier.

Results

The interhemispheric communication in the brain is achieved via the brain commissures, bundles of white matter linking the two cerebral hemispheres. Anterior white commissure (AWC)—related with olfactory and non-visual communication, hippocampal commissure—main efferent pathway of the hippocampus, connecting the hippocampal formation to structures beyond the temporal lobe, crucial in declarative memory formation and consolidation—and the corpus callosum (CC)—from the anterior commissure to the hippocampal commissure—are the main telencephalic commissures. Supramammilary commissure, posterior commissure, supraoptic commissure and habenular commissure are diencephalic commissures—unknown function, probably related to involuntary eye movements. Commissural agenesis (AWC is absent or impossible to recognize), Alzheimer’s Disease (hippocampal commissure may contribute for disease dissemination) and agenesis of corpus callosum are some of the disturbances that involve the telenchephalic commissures.

Conclusions

A comprehensive understanding of the clinic–anatomic correlation is pivotal to understand the pathology and therefore improve our diagnostic accuracy and treatment options, in the background of all patient management.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10

Similar content being viewed by others

References

  1. Acosta-Cabronero J, Nestor P (2014) Diffusion tensor imaging in Alzheimer’s disease: insights into the limbic-diencephalic network and methodological considerations. Front Aging Neurosci 2(6):266. https://doi.org/10.3389/fnagi.2014.00266. (eCollection 2014)

    Article  Google Scholar 

  2. Arbelaez A, Pajon A, Castillo M (2003) Acute Marchiafava-Bignami disease: MR findings in two patients. AJNR Am J Neuroradiol 24(10):1955–1957

    PubMed  PubMed Central  Google Scholar 

  3. Behpour Y (2012) Brain commissural anomalies. In: Mantamadiotis T (ed) When things go wrong—diseases and disorders of the human brain. InTech, Rijeka. https://doi.org/10.5772/33444

    Chapter  Google Scholar 

  4. Bénézit A, Hertz-pannier L, Dehaenelambertz G, Monzalvo K, Germanaud D, Duclap D, Guevara P, Mangin JF, Poupon C, Moutard ML, Dubois J (2015) Organising white matter in a brain without corpus callosum fibres. Cortex 63:155–171

    Article  PubMed  Google Scholar 

  5. Carrilho PE, Santos MB, Piasecki L, Jorge AC (2013) Marchiafava-Bignami disease: a rare entity with a poor outcome. Revista Brasileira de Terapia Intensiva 25(1):68–72

    Article  PubMed  PubMed Central  Google Scholar 

  6. Chiappedi M, Fresca A, Baschenis IM (2012) Complete corpus callosum agenesis: can it be mild?. Case Rep Pediatr 2012:752751

    PubMed  PubMed Central  Google Scholar 

  7. Christiansen K, Aggleton JP, Parker GD, O’sullivan MJ, Vann SD, Metzlerbaddeley C (2016) The status of the precommissural and postcommissural fornix in normal ageing and mild cognitive impairment: an MRI tractography study. Neuroimage 130:35–47

    Article  PubMed  Google Scholar 

  8. Christiansen K, Metzler-baddeley C, Parker GD, Muhlert N, Jones DK, Aggleton JP, Vann SD (2017) Topographic separation of fornical fibers associated with the anterior and posterior hippocampus in the human brain: an MRI diffusion study. Brain Behav 7(1):e00604

    Article  PubMed  Google Scholar 

  9. Corcoba A, Steullet P, Duarte JM, Van de Looij Y, Monin A, Cuenod M, Gruetter R, Do KQ (2015) Glutathione deficit affects the integrity and function of the fimbria/fornix and anterior commissure in mice: relevance for schizophrenia. Int J Neuropsychopharmacol 19(3):1–11

    Google Scholar 

  10. (2017) “Defining ‘peerness’ in peer-delivered health and wellness interventions for serious mental illness”: Correction to Muralidharan et al. (2017) Psychiatric Rehab J 40(2):215

  11. Di ieva A, Fathalla H, Cusimano MD, Tschabitscher M (2015) The indusium griseum and the longitudinal striae of the corpus callosum. Cortex 62:34–40

    Article  PubMed  Google Scholar 

  12. Fabri M, Pierpaoli C, Barbaresi P, Polonara G (2014) Functional topography of the corpus callosum investigated by DTI and fMRI. World J Radiol 6(12):895–906

    Article  PubMed  PubMed Central  Google Scholar 

  13. Fernández-Miranda JC, Rhoton AL, Álvarez-Linera J, Kakizawa Y, Choi C, de Oliveira EP (2007) Three dimensional microsurgical and tractographic anatomy of the white matter of the human brain. Neurosurgery 62(6):989–1028

    Google Scholar 

  14. Gerrish AC, Thomas AG, Dineen RA (2014) Brain white matter tracts: functional anatomy and clinical relevance. Semin Ultrasound CT MRI 35(5):432–444

    Article  Google Scholar 

  15. Heinrich A, Runge U, Khaw AV (2004) Clinicoradiologic subtypes of Marchiafava-Bignami disease. J Neurol 251(9):1050–1059

    Article  PubMed  Google Scholar 

  16. Huber GC, Crosby EC (1929) Somatic and visceral connections of the diencephalon. Arch Neurol Psychiatry 22(2):187–229

    Article  Google Scholar 

  17. Jang SH, Lee HD (2016) Compensatory neural tract from contralesional fornical body to ipsilesional medial temporal lobe in a patient with mild traumatic brain injury: a case report. Am J Phys Med Rehabil 95(2):e14–e17

    Article  PubMed  Google Scholar 

  18. Kasasbeh AS, Smyth MD, Steger-May K, Jalilian L, Bertrand M, Limbrick DD (2014) Outcomes after anterior or complete corpus callosotomy in children. Neurosurgery 74(1):17–28; (discussion 28)

    Article  PubMed  Google Scholar 

  19. Krupa K, Bekiesinska-Figatowska M (2013) Congenital and acquired abnormalities of the corpus callosum: a pictorial essay. Biomed Res Int. 2013:265619

    Article  PubMed  PubMed Central  Google Scholar 

  20. Lee SK, Mori S, Kim DJ, Kim SY, Kim SY, Kim DI (2004) Diffusion tensor MR imaging visualizes the altered hemispheric fiber connection in callosal dysgenesis. Am J Neuroradiol 25(1):25–28

    CAS  PubMed  PubMed Central  Google Scholar 

  21. Lövblad KO, Schaller K, Vargas MI (2014) The fornix and limbic system. Semin Ultrasound CT MRI 35(5):459–473

    Article  Google Scholar 

  22. Magis-weinberg L, Blakemore SJ, Dumontheil I (2017) Social and nonsocial relational reasoning in adolescence and adulthood. J Cogn Neurosci 29(10):1739–1754

    Article  PubMed  PubMed Central  Google Scholar 

  23. Montine T, Phelps C, Beach T, Bigio E, Cairns N, Dickson D (2012) National institute on Aging-Alzheimer’s association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach. Acta Neuropathol 123:1–11

    Article  CAS  PubMed  Google Scholar 

  24. Nelson P, Alafuzoff I, Bigio E, Bouras C, Braak H, Cairns N (2012) Correlation of Alzheimer disease neuropathologic changes with cognitive status: a review of the literature. J Neuropathol Exp Neurol 71:362–381

    Article  PubMed  Google Scholar 

  25. Nieuwenhuys R, Voogd J, van Huijzen C (1978) The human central nervous system. Springer, Berlin

    Book  Google Scholar 

  26. Nir T, Jahanshad N, Villalon-Reina J, Toga A, Jack C, Weiner M (2013) Effectiveness of regional DTI measures in distinguishing Alzheimer’s disease, MCI, and normal aging. NeuroImage Clin 3:180–195

    Article  PubMed  PubMed Central  Google Scholar 

  27. Ozdemir NG (2015) The anatomy of the posterior commissure. Turkish Neurosurg 25(6):837–843

    Google Scholar 

  28. Paidipati GMK (2014) Magnetic resonance imaging in marchiafava-bignami syndrome: a cornerstone in diagnosis and prognosis. Case Rep Radiol 2014:609708

    Google Scholar 

  29. Pearce JM (2007) Corpus callosum. Eur Neurol 57(4):249–250

    Article  CAS  PubMed  Google Scholar 

  30. Pescatori L, Tropeano MP, Manfreda A, Delfini R, Santoro A (2017) Three dimensional anatomy of the white matter fibers of the temporal lobe: surgical implications. World Neurosurg 100:144–158

    Article  PubMed  Google Scholar 

  31. Plowey ED, Ziskin JL (2016) Hippocampal phospho-tau/MAPT neuropathology in the fornix in Alzheimer disease: an immunohistochemical autopsy study. Acta Neuropathol Commun 4(1):114

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Raybaud C (2010) The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation. Neuroradiology 52(6):447–477

    Article  PubMed  Google Scholar 

  33. Schmahmann JD, Smith EE, Eichler FS, Filley CM (2008) Cerebral white matter: neuroanatomy, clinical neurology, and neurobehavioral correlates. Ann N Y Acad Sci 1142:266–309

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Thomas AG, Koumellis P, Dineen RA (2011) The fornix in health and disease: an imaging review. Radiographics 31(4):1107–1121

    Article  PubMed  Google Scholar 

  35. Utsunomiya H, Yamashita S, Takano K, Okazaki M (2006) Arrangement of fiber tracts forming Probst bundle in complete callosal agenesis: report of two cases with an evaluation by diffusion tensor tractography. Acta Radiol 47(10):1063–1066

    Article  CAS  PubMed  Google Scholar 

  36. Van der Knap LJ, Van der Ham IJ (2011) How does the corpus callosum mediate interhemispheric transfer? A review. Behav Brain Res 223(1):211221

    Google Scholar 

  37. Wilde EA, Bigler ED, Haider JM, Chu Z, Levin HS, Li X, Hunter JV (2006) Vulnerability of the anterior commissure in moderate to severe pediatric traumatic brain injury. J Child Neurol 21(9):769–776

    Article  PubMed  Google Scholar 

  38. Winter TJ, Franz EA (2014) Implication of the anterior commissure in the allocation of attention to action. Front Psychol 5:432

    Article  PubMed  PubMed Central  Google Scholar 

  39. Yeo SS, Jang SH (2013) Neural reorganization following bilateral injury of the fornix crus in a patient with traumatic brain injury. J Rehabil Med 45(6):595–598

    Article  PubMed  Google Scholar 

  40. Zemmoura I, Velut S, François P (2012) The choroidal fissure: anatomy and surgical implications. Adv Tech Stand Neurosurg 38:97–113

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

LJP: Protocol/project development, Manuscript writing/editing. FV: Data collection or management. LM: Data collection or management. AI: Data collection or management. RM: Data collection or management. OE: Manuscript writing/editing. KVA: Manuscript writing/editing. NL: Data collection or management, Protocol/project development. AA: Data collection or management. AA: Data collection or management. UA: Data collection or management. CJ: Data collection or management. CM: Data collection or management. AM: Data collection or management. LM: Data collection or management. SN: Data collection or management. OR: Data collection or management. PR: Data collection or management. BS: Data collection or management. NS: Data collection or management.

Corresponding author

Correspondence to José Pedro Lavrador.

Ethics declarations

Conflict of interest

The authors whose names are listed immediately above certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Collaborators: Afonso de Almeida, Afonso Amorim, António Urbano, João Chaves, Mafalda Cardoso, Mariana Almeida, Miguel Lança, Nuno Soares, Raquel Oliveira, Raquel Pinto, Sara Brito, Sara Nabais.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lavrador, J.P., Ferreira, V., Lourenço, M. et al. White-matter commissures: a clinically focused anatomical review. Surg Radiol Anat 41, 613–624 (2019). https://doi.org/10.1007/s00276-019-02218-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00276-019-02218-7

Keywords

Navigation