Neuroanatomy, Corpus Callosum

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Andrea Goldstein
Benjamin Covington

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Fassil Mesfin

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6/28/2019 10:30:00 PM


The corpus callosum is the primary commissural region of the brain consisting of white matter tracts that connect the left and right cerebral hemispheres. It is composed of approximately 200 million heavily myelinated nerve fibers that form homotopic or heterotopic projections to contralateral neurons in the same anatomical layer. [1] During infancy, the corpus callosum expands rapidly due to an increase in the number of axons, axon diameter, and myelin. Although the development of the corpus callosum is complete by age four, growth continues until the third decade of life at a much slower rate. [1] Anatomically from anterior to posterior, the corpus callosum is composed of four parts based on previous histological findings: the rostrum, genu, body, and splenium, each responsible for connecting distinct areas of the cortex. The isthmus refers to the narrow region between the body and splenium in the posterior aspect of the corpus callosum. [2] Fibers of the genu cross over and give rise to the forceps minor, a connection between regions of the frontal cortices. [2] The fibers of the splenium move posteriorly and contribute to the forceps major, providing a connection between the occipital lobes. [3] The body fibers form the corona radiata as well as other large white matter pathways as they move transversely through the cerebral cortex. Finally, the orbital regions of the frontal lobes are connected via the rostral fibers. [3] Due to its anatomical location, the corpus callosum is strongly related to the fornix and lateral ventricles. In conjunction with the fornix, the corpus callosum forms a physical barrier to separate the two lateral ventricles. [3]

Structure and Function

Its main function is to integrate and transfer information from both cerebral hemispheres to process sensory, motor, and high-level cognitive signals. Advances have been made in learning more about the corpus callosum's role by studying callosotomy patients with partial or total hemispheric disconnection. [4] Based on these observations, the corpus callosum seems to be topographically organized, involved in the transfer of visual, auditory, and somatosensory information in posterior regions, and higher cognition is processing anteriorly. [4] There is evidence for the idea that the anterior callosal fibers transfer motor information between the frontal lobes, and the posterior fibers are involved in the processing of somatosensory (posterior midbody), auditory (isthmus) and visual (splenium) cues by connecting the parietal, temporal, and occipital lobes. [3] As the brain matures and white matter develops, the corpus callosum seems to play a crucial role in refining motor movements and cognitive functions. [3] Additional studies have shown that the corpus callosum has an inhibitory effect that normally prevents alien-hand syndrome and uncoordinated hand-motor behavior. [4]


The axons that form the corpus callosum arise primarily from neurons in neocortical layers II/III, V, and VI. [5] At 12 to 13 weeks of gestation, nerve fibers begin to cross the midline, giving rise to connections that later become the corpus callosum. By 18 weeks, all four components of the corpus callosum can be visualized using transvaginal sonogram. [6] There is some debate about the anatomic direction in which development progresses; some data support the hypothesis that the corpus callosum develops in the cranial/caudal direction while others have observed the opposite developmental pattern. Interestingly, the corpus callosum is present in all primates and evolved with the neocortex. [7]

Blood Supply and Lymphatics

The internal carotid artery network provides arterial blood supply to most of the corpus callosum, specifically via the pericallosal artery (a branch of the anterior cerebral artery). The splenium is the exception as it receives vascular input from the vertebrobasilar system. The terminal and choroidal branches of the posterior cerebral artery supply the splenium with arterial blood. Venous drainage occurs via the callosal and callosal cingular veins and ultimately the internal cerebral veins. [7]

Physiologic Variants

Physiologic variants of the corpus callosum include agenesis or hypoplasia. Agenesis of the corpus callosum is an uncommon brain malformation that either leads to a partial or total absence of the corpus callosum. Though rare, it is one of the more frequently occurring congenital malformations, affecting three to seven people per 1000 births. [7] A diagnosis can be made using prenatal ultrasound and can be concurrent with malformations in midline structures like cavum septum pellicidum, as well as cortical and posteror fossa abnormalities. [7] In part, it is the result of multiple developmental abnormalities, affecting steps as early as midline telencephalic patterning to later neuronal differentiation and axonal guidance. [5] The cause is unknown, but appears to be sporadic and possibly non-genetic. Despite the corpus callosum's crucial role in normal cognition, patients with isolated agenesis of the corpus callosum typically have good prognoses. Common deficits observed in this population include difficulty with problem-solving and socializing, often placing patients on the autism spectrum. [8] These deficits, known as "disconnection syndrome," are different from those observed in commissurotomy patients, who most notably have impaired bimanual coordinated motor activity. [5]  Currently, 55% to 70% of agenesis of the corpus callosum cases are not identified based on clinical features. Hypoplasia is most benign when the rostrum is absent and often is not clinically significant. Therefore, it is commonly an incidental finding in an MRI obtained for other clinical reasons. [5]

Surgical Considerations

A corpus callosotomy is a surgical procedure for patients with refractory disorders despite maximum medical managements. Also, it is the preferred surgical procedure for patients with refractory seizure disorder with drop attacks. Though controversial, some advocate for the surgical resection of the corpus callosum to treat low-grade gliomas as the migration patterns of these tumors typically involve the invasion of white matter tracts. 

Clinical Significance

The most common pathology associated with the corpus callosum is multiple sclerosis, resulting in demyelinating lesions in the corpus callosum and pericallosal region. Corpus callosum congenital anomalies are often associated with other brain defects, so evidence of an abnormality in corpus callosum development should prompt a workup for other potentially serious defects. In addition to the physiologic variants, corpus callosum lipomas are considered to be congenital malformations of the primitive meninges. Corpus callosum lipomas are classified as either curvilinear, which are usually located posteriorly and are asymptomatic, and tubolonodular, which are found anteriorly and associated with serious frontal abnormalities. Ischemia of the corpus callosum is uncommon due to vascular inputs from three main arteries: the anterior communicating, anterior pericallosal, and posterior cerebral arteries. However, ischemia can be caused by emboli, stenosis resulting from atherosclerotic plaques, or vasospasm of the supplying arteries. Ruptured aneurysms in the anterior cerebral or pericallosal arteries typically cause hemorrhages of the corpus callosum. Consequently, hematomas located in the anterior corpus callosum should be investigated using CT angiography or three-dimensional time of flight MR angiography. The corpus callosum has been implicated in many other pathologies as well. Marchiava-Bignami disease involves acute demyelination and necrosis of the corpus callosum, most commonly observed in the body region of the corpus callosum in patients with chronic alcoholism. Other toxins like carbon monoxide and drugs like cocaine and heroin have also been associated with demyelination and lesions in the corpus callosum. Other pathologies that can cause corpus callosum lesions and demyelination include exposure to certain viruses, metabolic dysfunction, and traumatic brain injury. The most common tumors found in the corpus callosum are glioblastomas, as well as lymphomas and metastases. [7]

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Neuroanatomy, Corpus Callosum - Questions

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Which of the following statements about the corpus callosum is incorrect?

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What is the term for the broad band of fibers connecting the two cerebral hemispheres?

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In the normal anatomy, which of the following is not an anatomical region of the corpus callosum?

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Neuroanatomy, Corpus Callosum - References


Developmental trajectory of the corpus callosum from infancy to the juvenile stage: Comparative MRI between chimpanzees and humans., Sakai T,Mikami A,Suzuki J,Miyabe-Nishiwaki T,Matsui M,Tomonaga M,Hamada Y,Matsuzawa T,Okano H,Oishi K,, PloS one, 2017     [PubMed]
Intra- and Inter-hemispheric Connectivity Supporting Hemispheric Specialization, Tzourio-Mazoyer N,,, 2016     [PubMed]
Neuroanatomy, neurophysiology, and central auditory assessment. Part III: Corpus callosum and efferent pathways., Musiek FE,, Ear and hearing, 1986 Dec     [PubMed]
Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes., Edwards TJ,Sherr EH,Barkovich AJ,Richards LJ,, Brain : a journal of neurology, 2014 Jun     [PubMed]
Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity., Paul LK,Brown WS,Adolphs R,Tyszka JM,Richards LJ,Mukherjee P,Sherr EH,, Nature reviews. Neuroscience, 2007 Apr     [PubMed]
The corpus callosum: white matter or terra incognita., Fitsiori A,Nguyen D,Karentzos A,Delavelle J,Vargas MI,, The British journal of radiology, 2011 Jan     [PubMed]
The corpus callosum: normal fetal development as shown by transvaginal sonography., Malinger G,Zakut H,, AJR. American journal of roentgenology, 1993 Nov     [PubMed]
Developmental changes in the corpus callosum from infancy to early adulthood: a structural magnetic resonance imaging study., Tanaka-Arakawa MM,Matsui M,Tanaka C,Uematsu A,Uda S,Miura K,Sakai T,Noguchi K,, PloS one, 2015     [PubMed]


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