The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation

Neuroradiology - Tập 52 Số 6 - Trang 447-477 - 2010
Charles Raybaud1
1Division of Neuroradiology, Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G1X8, Canada

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Rakic P, Yakovlev PI (1968) Development of the corpus callosum and cavum septi in man. J Comp Neurol 132:45–72

Déjerine J. Anatomie des Centres Nerveux, vol 1. Rueff, Paris, 1895. Masson, Paris, 1980, pp 119-120, 738-741 (reprint)

Silver J, Lorenz SE, Wahlsten D, Coughlin J (1982) Axonal guidance during development of the great cerebral commissures: descriptive and experimental studies, in vivo, on the role of preformed glial pathways. J Comp Neurol 210:10–29

Katz MJ, Lasek RJ, Silver J (1983) Ontophyletics of the nervous system: development of the corpus callosum and evolution of axon tracts. Proc Natl Acad Sci USA 80:5936–5940

Wahlsten D (1987) Defects of the fetal forebrain in mice with hereditary agenesis of the corpus callosum. J Comp Neurol 262:227–241

Hankin MH, Schneider BF, Silver J (1988) Death of the subcallosal glial sling is correlated with formation of the cavum septi pellucidi. J Comp Neurol 272:191–202

Koester SE, O’Leary DM (1994) Axons of early generated neurons in cingulate cortex pioneer the corpus callosum. J Neurosci 14:6608–6620

Livy DJ, Wahlsten D (1997) Retarded formation of the hippocampal commissure in embryos from mouse strains lacking a corpus callosum. Hippocampus 7:2–14

Shu T, Richards LJ (2001) Cortical axon guidance by the glial wedge during the development of the corpus callosum. J Neurosci 21:2749–2758

Richards LJ (2002) Axonal pathfinding mechanisms at the cortical midline and in the development of the corpus callosum. Braz J Med Biol Res 35:1431–1439

Shu T, Puche AC, Richards LJ (2003) Development of midline glial populations at the corticoseptal boundary. J Neurobiol 57:81–94

Shu T, Li Y, Keller A, Richards LJ (2003) The glial sling is a migratory population of developing neurons. Development 130:2929–2937

Richards LJ, Plachez C, Ren T (2004) Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human. Clin Genet 66:276–289

Lent R, Uziel D, Baudrimont M, Fallet C (2005) Cellular and molecular tunnels surrounding the forebrain commissures of human fetuses. J Comp Neurol 483:375–382

Ren T, Anderson A, Shen WB et al (2006) Imaging, anatomical and molecular analysis of callosal formation in the developing human fetal brain. Anat Record Part A 288A:191–204

Vulliemoz S, Raineteau O, Jahaudon D (2005) Reaching beyond the midline: why are human brains cross wired? Lancet Neurology 4:87–99

Abbie AA (1939) The origin of the corpus callosum and the fate of the structures related to it. J Comp Neurol 70:9–44

Ariëns Kappers CU, Huber GC, Crosby EC. The comparative anatomy of the nervous system of vertebrates including man, vol III. Hafner, New York, 1967

Sarnat HB, Netsky MG (1974) Evolution of the nervous system. Oxford University Press, New York

Romer AS, Parsons TS (1977) The vertebrate body. Saunders, Philadelphia

Aboitiz F (2003) Montiel J. One hundred million years of interhemispheric communication: the history of the corpus callosum Braz J Med Biol Res 36:409–420

Yakovlev PI (1968) Telencephalon “impar”, “semipar”, “totopar” (morphogenetic, tectogenetic, and architectonic definitions). Int J Neurol 6:245–265

Gloor P, Salanova V, Olivier A, Quesney LF (1993) The human dorsal hippocampal commissure. Brain 116:1249–1273

Amaral DG, Insausti R, Cowan WM (1984) The commissural connections of the monkey hippocampal formation. J Comp Neurol 224:307–336

Demeter S, Rosene DL, Van Hoesen GW (1985) Interhemispheric pathways of the hippocampal formation, presubiculum and entorhinal and posterior parahippocampal cortices in the rhesus monkey: the structure and organization of the hippocampal commissures. J Comp Neurol 233:30–47

Guénot M. Transfert interhémisphérique et agénésie du corps calleux. Capacités et limites de la commissure blanche antérieure. Neurochirurgie (Paris) 1998, 44(Suppl 1):113-115

Lamantia AS, Rakic P (1990) Cytological and quantitative characteristics of four cerebral commissures in the rhesus monkey. J Comp Neurol 291:520–537

Di Virgilio G, Clarke S, Pizzolato G, Schaffner T (1999) Cortical regions contributing to the anterior commissure in man. Exp Brain Res 124:1–7

Wilson CL, Isokawa M, Babb TL, Crandall PH. Functional connections in the human temporal lobe. I. Analysis of limbic system pathways using neuronal response evoked by electrical stimulation. Exp Brain Re 1990, 82:279-292

Wilson CL, Isokawa M, Babb TL et al (1991) Functional connections in the human temporal lobe. II. Evidence for a loss of functional linkage between contralateral limbic structures. Exp Brain Res 85:174–187

Spencer SS, Williamson PD, Spencer DD, Mattson RH (1987) Human hippocampal seizure spread studied by depth and subdural recording: the hippocampal commissure. Epilepsia 28:479–489

Phelps EA, Hirst W, Gazzaniga MS (1991) Deficits in recall following partial and complete commissurotomy. Cerebral cortex 1:492–498

Kier EL, Truwit CL (1997) The lamina rostralis: modification of concepts concerning the anatomy, embryology, and MR appearance of the rostrum of the corpus callosum. AJNR Am J Neuroradiol 18:715–722

Velut S, Destrieux C, Kakou M (1998) Anatomie morphologique du corps calleux. Neurochirurgie (Paris) 44(Suppl 1):17–30

Hofer S, Frahm J (2006) Topography of the human corpus callosum revisited—comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. NeuroImage 32:989–994

Kier L, Truwit CL (1996) The normal and abnormal genu of the corpus callosum: an evolutionary, embryologic, anatomic and MR analysis. AJNR Am J Neuroradiol 17:1631–1641

Aboitiz F, Scheibel AB, Fisher RS, Zaidel E (1992) Fiber composition of the corpus callosum. Brain Res 598:143–153

Widjaja E, Nilsson D, Blaser S, Raybaud C (2008) White matter abnormalities in children with idiopathic developmental delay. Acta Radiol 49:589–595

Jea A, Vachhrajani S, Widjaja E et al (2008) Corpus callosotomy in children and the disconnection syndromes: a review. Childs Nerv Syst 24:685–692

De Lacoste C, Kirkpatrick JB, Ross ED (1985) Topography of the human corpus callosum. J Neuropathol Exp Neurol 44:578–591

Oh JS, Park KS, Song IC et al (2005) Fractional anisotropy-based divisions of midsagittal corpus callosum. NeuroReport 16:317–320

Déjerine J. Anatomie des Centres Nerveux, vol 2, Rueff, Paris 1901. Masson, Paris 1980, pp 263-267 (reprint)

Liss L, Mervis L (1964) The ependymal lining of the cavum septi pellucidi: a histological and histochemical study. J Neuropathol Exp Neurol 23:355–367

Lancon JA, Haines DE, Lewis AI, Parent AD (1999) Endoscopic treatment of symptomatic septum pellucidum cysts: with some preliminary observations on the ultrastructure of the cyst wall: two technical reports. Neurosurgery 45:1251–1257

Ronsin E, Grosskopf D, Perre J (1997) Morphology and immunohistochemistry of a symptomatic septum pellucidum cavum Vergae cyst in man. Acta Neurochir 139:366–372

Shu T, Shen WB, Richards LJ (2001) Development of the perforating pathway: an ipsilaterally projecting pathway between the medial septum/diagonal band of Broca and the cingulate cortex that intersects the corpus callosum. J Comp Neurol 436:411–422

Yakovlev PI, Locke S (1961) nuclei of thalamus and connections of limbic cortex. III. Cortico-cortical connections of the anterior cingulate gyrus, the cingulum, and the subcallosal bundle in the monkey. Arch Neurol 5:364–400

Johnston TB (1934) A note on the peduncle of the flocculus and the posterior medullary velum. J Anat 68:471–479

Raybaud C, Girard N. Etude anatomique par IRM des agénésies and dysplasies commissurales télencéphaliques. Corrélations cliniques et interprétation morphogénétique. Neurochirurgie (Paris) 1998, 44(Suppl 1):38-60

Larroche JC, Baudey J (1961) septi pellucidi, cavum Vergae, cavum veli interpositi: cavités de la ligne médiane. Etude anatomique et pneumoencéphalographique dans la période néonatale. Biol Neonate 3:193–236

Shaw CM, Alvord EC (1969) Cava septi pellucidi et Vergae: their normal and pathological states. Brain 92:213–224

Scoffings DJ, Kurian KM (2008) Congenital and acquired lesions of the septum pellucidum. Clin Radiol 63:210–219

Auer RN, Gilbert JJ (1982) Cavum Vergae without cavum septi pellucidi. Arch Pathol Lab Med 106:462–463

Blakemore WF, Jolly RD (1972) The subependymal plate and associated ependyma in the dog. An ultrastructural study J Neurocytol 1:69–84

Hopewell JW (1975) The subependymal plate and the genesis of gliomas. J Pathol 117:101–103

Nishio S, Fujiwara S, Tashima T et al (1990) Tumors of the lateral ventricular wall, especially the septum pellucidum: clinical presentation and variations in pathological features. Neurosurgery 27:224–230

Aldur MM, Çelik HH, Sargon MF et al (1997) Unreported anatomical variation of septum pellucidum. Clin Anat 10:245–249

Bayer SA (2006) Altman J. Atlas of central nervous system development. The human brain during the late first trimester. CRC, Boca Raton

Bayer SA (2005) Altman J. Atlas of Central Nervous System Development. The human brain during the second trimester. CRC, Boca Raton

Shen WB, Plachez C, Mongi AS, Richards LJ (2006) Identification of candidate genes at the corticoseptal boundary during development. Gene Expres Patterns 6:471–481

Silver J, Ogawa MY (1983) Postnatally induced formation of the corpus callosum in acallosal mice on glia-coated cellulose bridges. Science 220:1067–1069

Tessier-Lavigne M, Goodman CS (1996) The molecular biology of axon guidance. Science 274:1123–1133

Lanier LM, Gates MA, Witke W et al (1999) Mena is required for neurulation and commissure formation. Neuron 22:313–325

Shu T (2003) Butz KG. Plachez et al Abnormal development of forebrain midline glia and commissural projections in Nfia knock-out mice J Neurosci 23:203–212

Jovanov-Milošević N, Čuljat M, Kostović I (2009) Growth of the human corpus callosum: modular and laminar morphogenetic zones. Frontiers Neuroanat 3:1–10

Pascual M, Pozas E, Barallobre J et al (2004) Coordinated functions of netrin-1 and class 3 secreted semaphorins in the guidance of reciprocal septohippocampal connections. Mol Cell Neurosci 26:24–33

Flanagan JG, van Vactor D (1998) Through the looking glass: axon guidance at the midline choice point. Cell 92:429–432

Kaprielian Z, Imondi R, Runko E (2000) Axon guidance at the midline of the developing CNS. Anat Rec (New Anat) 261:176–197

Probst M. Über den Bau des vollständigen balkenlosen Groβhirns sowie über Microgyrie und Heterotopie den Grauen Substanz. Arch Psychiat Nervenkr 1901, 34:709-786 (quoted by [70])

Probst FP (1973) Congenital defects of the corpus callosum. Acta Radiol Suppl 331:1–152

Onufrowicz W. Das balkenlose Microcephalengehirn. Arch J Psychiat 1887, 18:305-328 (quoted by [47])

Sachs H. Das Hemisphärenmark des Menschlichen Grosshirns. I. der Hinterhauptlappen. Leipzig, 1892 (quoted by [2])

Nakata Y, Barkovich AJ, Wahl M et al (2009) Diffusion abnormalities and reduced volume of the ventral cingulum bundle in agenesis of the corpus callosum: a 3T imaging study. AJNR Am J Neuroradiol 30:1142–1148

Mufson EJ, Pandya DN (1984) Some observations on the course and composition of the cingulum bundle in the rhesus monkey. J Comp Neurol 225:31–43

Dávila-Gutiérrez G (2002) Agenesis and dysgenesis of the corpus callosum. Sem Ped Neurol 9:292–301

Barkovich AJ, Simon EM, Walsh CA (2001) Callosal agenesis with cyst. A better understanding and new classification. Neurology 56:220–227

Pavone P, Barone R, Baieli S et al (2005) Callosal anomalies with interhemispheric cysts: expanding the phenotype. Acta Paediat 94:1066–1072

Sener RN (1993) Septo-optic dysplasia associated with total absence of the corpus callosum: MR and CT features. Eur Radiol 3:551–553

De León GA, Radkowski MA, Gutierrez FA (1995) Single forebrain ventricle without prosencephaly: agenesis of the corpus callosum with dehiscent fornices. Acta Neuropathol 89:454–458

Aicardi J (1996) Aicardi syndrome. In: Guerrini R et al (eds) Dysplasias of cerebral cortex and epilepsy. Lippincott-Raven, Philadelphia, pp 211–216

Truwit CL, Barkovich AJ (1990) Pathogenesis of intracranial lipomas: an MR study in 42 patients. AJNR Am J Neuroradiol 11:665–674

Osaka K, Handa H, Matsumoto S, Yasuda M (1980) Development of the cerebrospinal fluid pathway in the normal and abnormal human embryo. Child’s Brain 6:26–38

McLone DG (1980) The subarachnoid space: a review. Child’s Brain 6:113–130

Tart RP, Quisling RG (1991) Curvilinear and tubulonodular varieties of lipoma of the corpus callosum: an MR and CT study. J Comput Assist Tomogr 15:805–810

Demaerel P, Van de Gaer P, Wilms G, Baert AL (1996) Interhemispheric lipoma with variable callosal dysgenesis: relationship between embryology, morphology and symptomatology. Eur Radiol 6:904–909

De Morsier G (1956) Etudes sur les dysraphies crânio-encéphaliques. III Agénésie du septum lucidum avec malformation du tractus optique La dysplasie septo-optique Schweiz Arch Neurol Psychiat 77:267–292

Fernandes M, Hébert JM (2008) The ups and downs of holoprosencephaly: dorsal versus ventral patterning forces. Clin Genet 73:413–23

Kelberman D, Dattani MT (2008) Septo-optic dysplasia—novel insights into the aetiology. Horm Res 69:257–265

Schachter KA, Krauss RS (2008) Murine models of holoprosencephaly. Curr Top Develop Biol 84:139–170

Hoyt WF, Kaplan SL, Grumbach MM, Glaser JS. Septo-optic dysplasia and pituitary dwarfism. Lancet 1970, 1:893-894 (letter)

Acers TE (1981) Optic nerve hypoplasia: septo-optic-pituitary dysplasia syndrome. Tr Am Ophth Soc 79:425–457

Barkovich AJ, Fram EK, Norman D (1989) Septo-optic dysplasia: MR imaging. Radiology 171:189–192

Williams J, Brodsky MC, Griebel M et al (1993) Septo-optic dysplasia: the clinical insignificance of an absent septum pellucidum. Dev Med Child Neurol 35:490–501

Belhocine O, André C, Khalifa G, Adamsbaum C (2005) Does asymptomatic septal agenesis exist? A review of 34 cases. Pediatr Radiol 35:410–418

Supprian T, Sian J, Heils A et al (1999) Isolated absence of the septum pellucidum. Neuroradiology 41:563–566

Raybaud C, Girard N, Levrier O et al (2001) Schizencephaly: correlation between the lobar topography of the cleft(s) and absence of the septum pellucidum. Childs Nerv Syst 17:217–222

Bodensteiner JB (1995) The saga of the septum pellucidum: a tale of unfunded clinical investigations. J Child Neurol 10:227–231

Bodensteiner JB, Schaefer GB, Craft JM (1998) Cavum septi pellucidi and cavum Vergae in normal and developmentally delayed populations. J Child Neurol 13:120–121

Miller E, Widjaja E, Blaser S et al (2008) The old and the new: supratentorial MR findings in Chiari II malformation. Childs Nerv Syst 24:563–575

Vachha B, Adams RC, Rollins NK (2006) Limbic tract anomalies in pediatric myelomeningocele and Chiari II malformation: anatomic correlation with memory and learning—initial investigation. Radiology 240:194–202

Raybaud C (1982) Cystic malformations of the posterior fossa—abnormalities associated with development of the roof of the fourth ventricle and adjacent meningeal structures. J Neuroradiol 9:103–133

Michaud J, Mizrahi EM, Urich H (1982) Agenesis of the vermis with fusion of the cerebellar hemispheres, septo-optic dysplasia and associated anomalies. Report of a case Acta Neuropathol (Berl) 56:161–166

Jellinger KA (2002) Rhombencephalosynapsis. Acta Neuropathol 103:305–6

Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen MM Jr (1996) Frontonasal dysplasia: analysis of 21 cases and literature review. Int J Oral Maxillofac Surg 25:91–97

Wu E, Vargevik K, Slavotinek AM (2007) Subtypes of frontonasal dysplasia are useful in determining clinical prognosis. Am J Clin Genet Part A 143A:3069–3078

Koenig SB, Naidich TP, Lissner G (1982) The morning glory syndrome associated with sphenoidal cephalocele. Ophtalmology 89:1368–1373

Vermeulen RJ, Wilke M, Horber V, Krägeloh-Mann I (2010) Microcephaly with simplified gyral pattern. MRI classification Neurology 74:386–391

Kappeler C, Dhenain M (2007) Phan Dinh Tuy F et al. Magnetic resonance imaging and histological studies of corpus callosum and hippocampal abnormalities linked to doublecortin deficiency J Comp Neurol 500:239–254

Kitamura K, Yanazawa M, Sugiyama N et al (2002) Mutation in ARX causes abnormal development of brain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans. Nat Genet 32:359–369

Miyata H, Chute DJ, Fink J et al (2004) Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia. Acta Neuropathol 107:69–81

Sato N, Ota M, Yagishita A et al (2008) Aberrant midsagittal fiber tracts in patients with hemimegalencephaly. AJNR Am J Neuroradiol 29:823–827

Robin NH, Taylor CJ, McDonald-McGinn et al. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet Part A 2006, 140A:2416-2425

Barkovich AJ, Kuzniecky RI, Jackson GD et al (2005) A developmental and genetic classification for malformations of cortical development. Neurology 65:1873–1887

Pierson TM, Zimmerman RA, Tennekoon GI, Bönnemann CG (2008) Mega-corpus callosum, polymicrogyria, and psychomotor retardation: confirmation of a syndromic entity. Neuropediatrics 39:123–127

Online Mendelian Inheritance in Man, OMIM (TM). McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/

Schmid RS, Maness PF (2008) L1 and NCAM adhesion molecules as signaling co-receptors in neuronal migration and process outgrowth. Curr Opin Neurobiol 18:245–250

Fransen E, Van Camp G, Vits L, Willems PJ (1997) L1-associated diseases: clinical geneticists divide, molecular geneticists unite. Hum Mol Genet 6:1625–1632

Yamasaki M, Thompson P, Lemmon V (1997) CRASH syndrome: mutations in L1CAM correlate with severity of the disease. Neuropediatrics 28:175–178

Weller S, Gärtner J (2001) Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): mutations in the L1CAM gene. Hum Mutat 18:1–12

Reed UC (2009) Congenital muscular dystrophy. Part II: a review of pathogenesis and therapeutic perspectives. Arq Neuropsiquiatr 67:343–362

Raybaud C, Di Rocco C (2007) Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review. Childs Nerv Syst 23:1379–1388

Doherty P, Wlash F (1996) CAM-FGF receptor interaction: a model for axonal growth. Mol Cell Neurosci 8:99–111

Kamiguchi H, Lemmon V (1997) Neural cell adhesion molecule L1: signaling pathways and growth cone motility. J Neurosc Res 49:1–8