|prognosis = Varies by type and severity; anencephaly is fatal, while mild spina bifida may have normal lifespan
|frequency =
|frequency = ~1 in 1,000 births globally (varies by region and folate intake)
|deaths =
|deaths = High mortality in severe forms (e.g., anencephaly is incompatible with life)
}}
}}
'''Colpocephaly''' is a [[cephalic disorder]] involving the disproportionate enlargement of the [[Posterior horn of lateral ventricle|occipital horns]] of the [[lateral ventricles]] and is usually diagnosed early after birth due to [[Epileptic seizures|seizures]]. It is a nonspecific finding and is associated with multiple [[neurological disorder|neurological syndromes]], including [[agenesis of the corpus callosum]], [[Chiari malformation]], [[lissencephaly]], and [[microcephaly]].<ref name=volpe>{{cite journal|last=Volpe|first=P|author2=Paladini, D.|author3=Resta, M.|author4=Stanziano, A.|author5=Salvatore, M.|author6=Quarantelli, M.|author7=Gentile, M.|title=Characteristics, associations and outcome of partial agenesis of the corpus callosum in the fetus.|journal=Ultrasound in Obstetrics & Gynecology |year=2006|volume=27|issue=5|pages=509–516|doi=10.1002/uog.2774|pmid=16619387}}</ref> Although the exact cause of colpocephaly is not known yet, it is commonly believed to occur as a result of [[neuronal migration disorders]] during early brain development, [[Uterus|intrauterine]] disturbances, perinatal injuries, and other [[central nervous system]] disorders.<ref name=puvab>{{cite journal|last=Puvabanditsin |first=Surasak |author2=Garrow, Eugene |author3=Ostrerov, Yuliya |author4=Trucanu, Dumitru |author5=Ilic, Maja |author6=Cholenkeril, John V.|title=Colpocepepahly:a case report|journal=American Journal of Perinatology|year=2006|volume=23|issue=5|pages=295–297|doi=10.1055/s-2006-947161}}</ref> Individuals with colpocephaly have various degrees of motor disabilities, visual defects, [[spasticity]], and moderate to severe [[intellectual disability]].<ref name=bodensteiner>{{cite journal|last=Bodensteiner|first=J|author2=Gay, C.T|title=Colpocephaly: pitfalls in the diagnosis of a pathologic entity utilizing neuroimaging techniques|journal=Journal of Child Neurology|year=1990|volume=5|issue=2|pages=166–168|doi=10.1177/088307389000500221|pmid=2345283}}</ref>
No specific treatment for colpocephaly exists, but patients may undergo certain treatments to improve their motor function or intellectual disability.
== Symptoms ==
[[File:Agenesis.jpg|thumb|alt= Agenesis of the corpus callosum |Agenesis of the corpus callosum]]
There are various symptoms of colpocephaly and patients can experience effects ranging from mild to severe. Some patients do not show most of the symptoms related to colpocephaly, such as psychomotor abnormalilities and agenesis of the corpus callosum. In some cases, signs appear later on in life and a significant number of children suffer only from minor disabilities.
[[File:Agenesis.jpg|thumb|alt= Agenesis of the corpus callosum |Agenesis of the corpus callosum|left]]
The following list includes common symptoms of colpocephaly.<ref name=bodensteiner /><ref name=landman>{{cite journal|last=Landman|first=J|author2=Weitz, R.|author3=Dulitzki, F.|author4=Shuper, A.|author5=Sirota, L.|author6=Aloni, D.|author7=Gadoth, N.|title=Radiological colpocephaly: a congenital malformation or the result of intrauterine and perinatal brain damage|journal=Brain Development|year=1989|volume=11|issue=5|pages=313–316|doi=10.1016/s0387-7604(89)80059-2}}</ref><ref>{{cite journal|last=Noorani|first=P|author2=Bodensteiner, J. B. |author3=Barnes, P. D |title=Colpocephaly: frequency and associated findings|journal=Journal of Child Neurology|year=1988|volume=3|issue=2|pages=100–104|doi=10.1177/088307388800300204|pmid=3259595}}</ref>
'''Colpocephaly''' is a rare [[neurological disorder]] characterized by an abnormal enlargement of the occipital horns of the [[lateral ventricles]] in the [[brain]]. This condition is often associated with a reduction in the white matter of the posterior cerebrum, leading to a distinctive appearance on [[neuroimaging]] studies.
* partial or complete agenesis of the corpus callosum
==Pathophysiology==
* intellectual disability
Colpocephaly results from an abnormal development of the [[cerebral cortex]] and the [[ventricular system]] during fetal development. The condition is thought to arise due to a disturbance in the normal migration of [[neurons]] during the second trimester of pregnancy. This disruption can lead to a disproportionate enlargement of the occipital horns of the lateral ventricles, while the frontal horns remain normal or are less affected.
* motor abnormalities
* visual defects such as, crossing of the eyes, missing visual fields, and [[optic nerve hypoplasia]]
* spasticity
* [[Epileptic seizures|seizures]]
* [[cerebral palsy]]
Intracranial abnormalities include:
==Clinical Features==
Individuals with colpocephaly may present with a variety of [[neurological symptoms]], which can vary in severity. Common clinical features include:
* [[Microcephaly]]
* [[Microcephaly]]
* [[Agenesis of the corpus callosum]]
* [[Intellectual disability]]
* [[Spina Bifida|Meningomyelocele]]
* [[Seizures]]
* [[Lissencephaly]]
* [[Motor skill]] impairments
* [[Periventricular leukomalacia]] (PVL)
* [[Visual impairment]]
* Enlargement of the [[cisterna magna]]
* [[Cerebellar hypoplasia]]
== Causes ==
The severity of symptoms often correlates with the extent of the underlying brain malformation.
There is no known definitive single mechanism that causes colpocephaly. However, researchers believe there are many possible causes of colpocephaly. It is a common symptom of other [[neurology|neurological]] disorders in newborns, can be caused as a result of shunt treatment of [[hydrocephalus]], [[developmental disorder]]s in [[premature birth|premature infants]], due to intrauterine disturbances during [[pregnancy]], genetic disorders, underdevelopment or lack of white matter in the [[cerebrum]], and exposure of the mother and the developing [[fetus]] to medications, infections, [[radiation]], or [[Poison|toxic substances]].<ref>{{cite journal|last=Cheong|first=Jin Hwan|author2=Kim, Choong Hyun |author3=Yang, Mun Sul |author4=Kim, Jae Min. |title=Atypical meningioma in the posterior fossa associated with colpocephaly and agenesis of the corpus callosum|journal=Acta Neurochirurgica. Supplement|year=2012|volume=113|pages=167–171|doi=10.1007/978-3-7091-0923-6_33|pmid=22116445|series=Acta Neurochirurgica Supplementum|isbn=978-3-7091-0922-9}}</ref> Also, it is usually more common in premature infants than in full-term infants, especially in babies born with [[cerebral hypoxia|hypoxia]] or lung immaturity.
Some of the [[central nervous system]] disorders which are associated with colpocephaly are as follows:<ref name=bodensteiner />
==Diagnosis==
* [[polymicrogyria]]
Colpocephaly is typically diagnosed through [[neuroimaging]] techniques such as [[magnetic resonance imaging]] (MRI) or [[computed tomography]] (CT) scans. These imaging modalities reveal the characteristic enlargement of the occipital horns of the lateral ventricles. In some cases, prenatal diagnosis is possible through [[ultrasound]] imaging.
* [[Periventricular leukomalacia]] (PVL)
* [[intraventricular hemorrhage]]
* [[Hydrocephalus]]
* [[schizencephaly]]
* [[microgyria]]
* [[microcephaly]]
* [[Pierre-Robin syndrome]]
* [[Neurofibromatosis]]
Often colpocephaly occurs as a result of [[hydrocephalus]]. Hydrocephalus is the accumulation of [[cerebrospinal fluid]] (CSF) in the [[Ventricular system|ventricles]] or in the [[subarachnoid space]] over the [[brain]]. The increased pressure due to this condition dilates occipital horns causing colpocephaly.
==Etiology==
The exact cause of colpocephaly is not well understood, but it is believed to be related to genetic and environmental factors that affect brain development. Some cases have been associated with [[chromosomal abnormalities]] or [[genetic syndromes]].
The most generally accepted theory is that of neuronal migration disorders occurring during the second to fifth months of fetal life. Neuronal migration disorders are caused by abnormal [[cell migration|migration]], [[cell proliferation|proliferation]], and organization of [[neuron]]s during early brain development. During the seventh week of [[gestation]], neurons start proliferating in the germinal matrix which is located in the [[subependymal zone|subependymal]] layer of the walls of the lateral ventricles. During the eighth week of gestation, the neurons then start migrating from the germinal zone to [[cerebral cortex|cortex]] along specialized radial [[neuroglia|glial fibers]]. Next, neurons organize themselves into layers and form synaptic contacts with other neurons present in the cortex. Under normal conditions, the neurons forming a [[germ layer|germinal layer]] around ventricles migrate to the surface of the brain and form the [[cerebral cortex]] and [[basal ganglia]]. If this process is abnormal or disturbed it could result in the enlargement of the occipital horns of the lateral ventricles. Common prenatal disturbances that have been shown to disturb the neuronal migration process include the following:<ref name=bodensteiner /><ref name=landman/><ref name=sonoworld>{{cite web|last=Joffe|first=Gary|title=Colpocephaly|url=http://www.sonoworld.com/fetus/page.aspx?id=100}}</ref><ref name=singhal />
==Management==
There is no cure for colpocephaly, and treatment is primarily supportive and symptomatic. Management strategies may include:
* continuation of [[oral contraceptive pill|oral contraceptives]]
* [[Anticonvulsant]] medications for seizure control
* exposure to alcohol
* [[Physical therapy]] to improve motor skills
* intrauterine [[malnutrition]]
* [[Occupational therapy]]
* intrauterine infections such as [[toxoplasmosis]]
* [[Speech therapy]]
* maternal drug ingestion during early pregnancy such as [[corticosteroid]]s, [[salbutamol]], and [[theophylline]]
* Educational support for cognitive and learning difficulties
Researchers also believe that these factors can cause destruction of neural elements that have previously been normally formed.<ref name=patnaik>{{cite journal|last=Patnaik|first=A|author2=Mishra SS|author3=Mishra S|author4=Das S.|title=A rare case of colpocephaly with macrocephaly successfully treated with ventriculo-peritoneal shunting|journal=Journal of Pediatric Neurosciences|year=2012|volume=7|issue=2|pages=150–1|doi=10.4103/1817-1745.102585|pmid=23248702|pmc=3519080}}</ref>
It is suggested that the underdevelopment or lack of white matter in the developing fetus could be a cause of colpocephaly. The partial or complete absence of white matter, also known as [[agenesis of the corpus callosum]] results in anatomic malformations that can lead to colpocephaly. This starts to occur around the middle of the second month to the fifth month of [[pregnancy]]. The lateral ventricles are formed as large cavities of the [[cerebrum|telencephalic vesicle]]. The size of the ventricles are decreased in normal development after the formation of the [[Median aperture|Foramen of Magendie]], which decompresses the ventricular cavities. [[Myelination]] of the ventricular walls and [[association fibers]] of the [[corpus callosum]] and the [[calcarine fissure]] helps shape the occipital horns. In cases where this developmental process is interrupted, occipital horns are disproportionately enlarged.<ref name=landman/>
==Prognosis==
The prognosis for individuals with colpocephaly varies widely depending on the severity of the condition and the presence of associated abnormalities. Some individuals may lead relatively normal lives with mild symptoms, while others may have significant disabilities.
Colpocephaly has been associated with [[chromosomal abnormalities]] such as [[trisomy 8|trisomy 8 mosaic]] and [[trisomy 9]] mosaic.<ref name=landman /> A few reports of genetically transmitted colpocephaly are also found in literature. Some of these are of two siblings, [[monozygotic]] twins, and non-identical twins. The authors suggest a genetic origin with an autosomal or [[X-linked recessive inheritance]] rather than resulting from early prenatal disturbances.<ref name=cerullo>{{cite journal|last=Cerullo|first=A|author2=Marini, C. |author3=Cevoli, S. |author4=Carelli, V. |author5=Montagna, P. |author6=Tinuper, P. |title=Colpocephaly in two siblings: further evidence of a genetic transmission|journal=Developmental Medicine & Child Neurology|year=2000|volume=42|issue=4|pages=280–282|doi=10.1017/s0012162200000487|pmid=10795569}}</ref><ref name=kang>{{cite journal|last=Kang|first=Y|author2=Kim, J. |author3=Park, M. |title=P05.10:Colpocephaly in non-identical twin following IVF-ET: a case report|journal=Ultrasound in Obstetrics & Gynecology|year=2010|volume=36|series=1|pages=187|doi=10.1002/uog.8372}}</ref>
==Related pages==
== Diagnosis ==
* [[Lissencephaly]]
* [[Holoprosencephaly]]
===Presentation===
* [[Microcephaly]]
[[File:Slide1oo.JPG|thumb|alt= Corpus callosum |Corpus callosum]]
* [[Ventriculomegaly]]
Colpocephaly is characterized by disproportionately large occipital horns of the lateral ventricles (also frontal and temporal ventricles in some cases). MRI and CT scans of patients demonstrate abnormally thick [[gray matter]] with thin poorly myelinated [[white matter]]. This happens as a result of partial or complete absence of the [[corpus callosum]]. Corpus callosum is the band of white matter connecting the two [[cerebral hemispheres]]. The corpus callosum plays an extremely important role in interhemispheric communication, thus lack of or absence of these neural fibers results in a number of disabilities.<ref name=herskowitz>{{cite journal|last=Herskowitz|first=J|author2=Rosman, N. P. |author3=Wheeler, C. B. |title=Colpocephaly: clinical, radiologic, and pathogenetic aspects|journal=Neurology|year=1985|volume=35|issue=11|pages=1594–1968|doi=10.1212/wnl.35.11.1594}}</ref>
The lemon sign on CT scans of patients refers to the shape of the fetal skull when the frontal bones lose their normal convex contour and appear flattened or inwardly scalloped. This gives the skull a shape similar to that of a lemon. The sign is seen on transverse [[medical ultrasonography|sonograms]] of the fetal cranium obtained at the level of the ventricles.
A special case is found in literature where [[lissencephaly]], colpocephaly, and [[Septo-optic dysplasia|septal agenesis]] are all present together. The CT scans of the patient shows the ventricular system having a unique appearance of a crown of a king. This is referred to as the 'CROWN SIGN'.<ref name=singhal>{{cite journal|last=Singhal |first=Namit |author2=Agarwal, Sunil |title=Septal agenesis and lissencephaly with colpocephaly presenting as the 'Crown Sign'|journal=Journal of Pediatric Neurosciences|year=2010|volume=5|issue=2|pages=121–123|doi=10.4103/1817-1745.76106|pmid=21559156|pmc=3087987}}</ref>
=== Prenatal ===
Diagnosing colpocephaly prenatally is difficult because in many cases signs start to appear after birth. Prenatal diagnosis is made by detecting enlargement of either or both occipital horns of the lateral ventricles. Usually prenatal ultrasounds don't show cephalic abnormalities and in cases that they do show abnormality is of low accuracy, making it difficult to diagnose colpocephaly. Often, abnormalities in prenatal ultrasounds can be misdiagnosed as hydrocephalus.<ref name=puvab />
=== Postnatal ===
After birth, MR imaging can be done to look for cephalic abnormalities. This is the most commonly used method for diagnosing colpocephaly. Physicians look for abnormally large occipital horns of the lateral ventricles and diminished thickness of white matter.<ref name=herskowitz /> [[Lumbar puncture|Spinal tapping]] is not a preferred method for diagnosis because newborn babies with colpocephaly or hydrocephaly have open [[fontanelle]]s which makes it difficult to collect CSF. Also, colpocephaly is not associated with increased pressure.<ref name="ReferenceA">de Grauw, Ton. Pediatric Neurosciences</ref>
== Treatment ==
Colpocephaly is usually non-fatal. There has been relatively little research conducted to improve treatments for colpocephaly, and there is no known definitive treatment of colpocephaly yet. Specific treatment depends on associated symptoms and the degree of dysfunction. [[Anticonvulsant]] medications can be given to prevent seizure complications, and physical therapy is used to prevent contractures (shrinkage or shortening of muscles) in patients that have limited mobility. Patients can also undergo surgeries for stiff joints to improve motor function. The prognosis for individuals with colpocephaly depends on the severity of the associated conditions and the degree of abnormal brain development.<ref name="ReferenceA"/>
A rare case of colpocephaly is described in literature which is associated with [[macrocephaly]] instead of microcephaly. Increased intracranial pressure was also found in the condition. Similar symptoms (absence of corpus callosum and increased head circumference) were noted as in the case of colpocephaly that is associated with microcephaly. A bi-ventricular peritoneal shunt was performed, which greatly improved the symptoms of the condition. Ventriculo-peritoneal shunts are used to drain the fluid into the [[peritoneal cavity]].<ref name=patnaik />
== History ==
These brain abnormalities were first described by Benda in 1940 as 'vesiculocephaly'. In 1946, Yakovlev and Wadsworth coined the term colpocephaly from the Greek word ''kolpos'' (hollow) and ''kephalos'' (head).{{Source?|reason=In Greek κεφαλή is head. What is the source for this erroneous information?|date=February 2019}} It was suggested that the enlargement of ventricles occurred as a result of [[white matter]] development arrest during early fetal life.<ref name=landman /> They stated that “in the apparent dilatation of the occipital horns...it represented a failure of development of the cerebral wall with persistence of the embryonal vesicular character of the brain." Yakovlev meant for this term to apply to the end result of disturbances during the development of the brain. He suggested the term 'hydrocephalus ex vauco' to be used for enlargement of the occipital horns of the lateral ventricles as a result of damage to the brain after it is normally formed. However, today the term colpocephaly is used to describe both the situations.<ref name=sonoworld />
== Future Research ==
[[Stem cell]] therapy is considered a very promising treatment for patients with colpocephaly. [[Oligodendrocyte|Oligodendroglial cells]] can be used which will increase the production of [[myelin]] and alleviate symptoms of colpocephaly. Damage to the developing oligodendrocytes near the cerebral ventricles causes cerebral palsy as well as other [[demyelinating diseases]] such as [[multiple sclerosis]] and [[leukodystrophies]]. Demyelination reduces the speed of conduction in affected nerves resulting in disabilities in cognition, sensation, and motor. Therefore, by using oligodendrocyte stem cells the effects of cerebral palsy can be treated and other symptoms of colpocephaly can be alleviated.<ref name="ReferenceA"/>
Varies by type and severity; anencephaly is fatal, while mild spina bifida may have normal lifespan
Frequency
~1 in 1,000 births globally (varies by region and folate intake)
Deaths
High mortality in severe forms (e.g., anencephaly is incompatible with life)
Agenesis of the corpus callosum
Colpocephaly is a rare neurological disorder characterized by an abnormal enlargement of the occipital horns of the lateral ventricles in the brain. This condition is often associated with a reduction in the white matter of the posterior cerebrum, leading to a distinctive appearance on neuroimaging studies.
Colpocephaly results from an abnormal development of the cerebral cortex and the ventricular system during fetal development. The condition is thought to arise due to a disturbance in the normal migration of neurons during the second trimester of pregnancy. This disruption can lead to a disproportionate enlargement of the occipital horns of the lateral ventricles, while the frontal horns remain normal or are less affected.
Colpocephaly is typically diagnosed through neuroimaging techniques such as magnetic resonance imaging (MRI) or computed tomography (CT) scans. These imaging modalities reveal the characteristic enlargement of the occipital horns of the lateral ventricles. In some cases, prenatal diagnosis is possible through ultrasound imaging.
The exact cause of colpocephaly is not well understood, but it is believed to be related to genetic and environmental factors that affect brain development. Some cases have been associated with chromosomal abnormalities or genetic syndromes.
The prognosis for individuals with colpocephaly varies widely depending on the severity of the condition and the presence of associated abnormalities. Some individuals may lead relatively normal lives with mild symptoms, while others may have significant disabilities.
