Chiari malformation

Findings are due to brainstem and lower cranial nerve dysfunction. The onset of symptoms is less likely to be present during adulthood in most patients. Younger children generally have a substantially different presentation of clinical symptoms from older children. Younger children are more likely to have a more rapid neurological degeneration with profound brainstem dysfunction over several days. Headache is the most common symptom in those with Chiari malformation type 1 (in which only the cerebellar tonsils descend below the foramen magnum). This headache is usually occipital or sub-occipital in location (but may also present in other cranial areas), is usually dull or throbbing and is characteristically associated with Valsalva maneuvers (such as bearing down, coughing, sneezing, bending over, or forcefully exhaling against a closed airway). Considering a headache is one of the most common symptoms, it is important to note that a tension headache is also a common repetitive sign before diagnosis. Symptoms that may be due to Chiari malformations include: • Neurogenic dysphagia: Difficulty swallowing. • Cyanosis: Bluish discoloration of skin while feeding. • Weak crying • Facial weakness • Aspiration • Headaches aggravated by Valsalva maneuvers • Tinnitus (ringing in the ears) • Lhermitte's sign (electrical sensation that runs down the back and into the limbs) • Vertigo (dizziness) • Nausea • Schmahmann's syndrome • Nystagmus (irregular eye movements; typically, so-called "downbeat nystagmus") • Facial pain • Muscle weakness • Impaired gag reflex • Dysphagia (difficulty swallowing) • Restless leg syndrome • Sleep apnea • Sleep disorders • Impaired coordination • Severe cases may develop all the symptoms and signs of a bulbar palsy • Paralysis due to pressure at the Cervico-medullary junction may progress in a so-called "clockwise" fashion, affecting the right arm, then the right leg, then the left leg, and finally the left arm; or the opposite way around. • Papilledema on fundoscopic exam due to increased intracranial pressure • Pupillary dilation • Dysautonomia: tachycardia (rapid heart), syncope (fainting), polydipsia (extreme thirst), chronic fatigue • Apnea: Sudden pause of breathing, usually during sleep. • Opisthotonos: Spasm of the head which causes the head to arch backwards. More common in infants than in adults. • Stridor The blockage of cerebrospinal fluid (CSF) flow may also cause a syrinx to form, eventually leading to syringomyelia. Central cord symptoms such as hand weakness, dissociated sensory loss, and, in severe cases, paralysis may occur. Syringomyelia Syringomyelia is most often a chronic progressive degenerative disorder characterized by a fluid-filled cyst located in the spinal cord. However, there can also be cases where the syrinx, in terms of size and extent of symptoms, actually stays stable throughout a lifetime. Syringomyelia symptoms include pain, weakness, numbness, and stiffness in the back, shoulders, arms or legs. Other symptoms include headaches, the inability to feel changes in temperature, sweating, sexual dysfunction, and loss of bowel and bladder control. It is usually seen in the cervical region but can extend into the medulla oblongata and pons, or it can reach downward into the thoracic or lumbar segments. Syringomyelia is often associated with type I Chiari malformation and is commonly seen between the C-4 and C-6 levels. The exact development of syringomyelia is unknown, but many theories suggest that the herniated tonsils in type I Chiari malformations cause a "plug" to form, which does not allow an outlet of CSF from the brain to the spinal canal. Syringomyelia is present in 25% of patients with type I Chiari malformations. ==Pathophysiology==

The most common pathophysiological mechanism by which Chiari type I malformations occur is due to a congenitally small posterior fossa. Another pathophysiological mechanism by which Chiari malformations form is by negative pressure or a pulling force from below the foramen magnum, which pulls against the brain, causing the cerebellar tonsils to herniate past the foramen magnum. Causes of this negative or pulling pressure include a tethered cord or an excessively tense Filum terminale, a cerebrospinal fluid leak creating a negative pressure around the spinal cord as the fluid surrounding the cord leaks out, or a CSF-venous fistula, in which the CSF leaks into a nearby vein. Traumatic brain injury may cause delayed acquired Chiari malformation, but the pathophysiology of this is unknown. This is due to the fact that the condition can go asymptomatic for years and a diagnosis is often led through testing for a variety of symptoms. Additionally, ectopia may be present but asymptomatic until a whiplash injury causes it to become symptomatic. Other conditions linked to Chiari malformations include X-linked vitamin D-resistant rickets, and neurofibromatosis type I. ==Diagnosis==

Diagnosis is made through a combination of patient history, neurological examination, and medical imaging. Magnetic resonance imaging (MRI) is considered the preferred imaging modality for Chiari malformation. The MRI visualizes neural tissue such as the cerebellar tonsils and spinal cord as well as bone and other soft tissues. CT and CT myelography are other options and were used prior to the advent of MRI, unfortunately the resolution of CT based modalities do not characterize syringomyelia and other neural abnormalities as well. By convention, the cerebellar tonsil position is measured relative to the basion-opisthion line, using sagittal T1 MRI images or sagittal CT images. The selected cutoff distance for abnormal tonsil position is somewhat arbitrary, as not every person will be symptomatic at a certain amount of tonsil displacement, and the probability of symptoms and syrinx increases with greater displacement; however, greater than 5 mm is the most frequently cited cutoff number, though some consider 3–5 mm to be "borderline"; pathological signs and syrinx may occur beyond that distance. One study showed little difference in cerebellar tonsil position between standard recumbent MRI and upright MRI for patients without a history of whiplash injury. The diagnosis of a Chiari II malformation can be made prenatally, through ultrasound. Classification In the late 19th century, Austrian pathologist Hans Chiari described seemingly related anomalies of the hindbrain, the so-called Chiari malformations I, II and III. Later, other investigators added a fourth (Chiari IV) malformation. The scale of severity is rated I–IV, with IV being the most severe. Types III and IV are very rare. Since Dr. Chiari's original descriptions Chiari 0, 1.5, 3.5, and 5 have been described in the medical literature. Types of Chiari malformation Other conditions sometimes causally associated with Chiari malformation include hydrocephalus, syringomyelia, spinal curvature, tethered spinal cord syndrome, and connective tissue disorders such as Ehlers–Danlos syndrome and Marfan syndrome. Chiari malformation is the most frequently used term for this set of conditions. The use of the term "Arnold–Chiari malformation" has fallen somewhat out of favor over time, although it is used to refer to the type II malformation. Current sources use "Chiari malformation" to describe its four specific types, reserving the term "Arnold–Chiari" for type II only. Some sources still use "Arnold–Chiari" for all four types. Chiari malformation type 1 emerges during skull and brain development, often without symptoms until late childhood or adulthood. In contrast, the pediatric forms include type 2 and type 3, which are present from birth, making them congenital conditions. Chiari malformation or Arnold–Chiari malformation should not be confused with Budd–Chiari syndrome, a hepatic condition also named for Hans Chiari. In Pseudo-Chiari Malformation, leaking of CSF may cause displacement of the cerebellar tonsils and similar symptoms sufficient to be mistaken for a Chiari I malformation. ==Treatment==

While there is no current cure, the treatments for Chiari malformation are surgery and management of symptoms. Treatment is directed at the occurrence of clinical symptoms rather than the radiological findings. The presence of a syrinx is known to give specific signs and symptoms that vary from dysesthetic sensations to algothermal dissociation to spasticity and paresis. These are important indications that decompressive surgery is needed for patients with Chiari Malformation Type II. Type II patients have severe brainstem damage and rapidly diminishing neurological response. Decompressive surgery Re-operation may be needed in up to 6.8% of patients, and possible causes of re-operation include incomplete decompression and dural scarring. ==Epidemiology==

The incidence of congenital Chiari I malformation was previously believed to be in the range of one per 1000 births, but is likely much higher. Women are three times more likely than men to have a congenital Chiari malformation. Type II malformations are more prevalent in people of Celtic descent. Typically, an infant's brain weighs around 400g at birth and triples to 1100-1400g by age 11. At the same time, the cranium triples in volume from 500 cm3 to 1500 cm3 to accommodate the growing brain. During human evolution, the skull underwent numerous changes to accommodate the growing brain. The evolutionary changes included increased size and shape of the skull, decreased basal angle, and basicranial length. These modifications resulted in a significant reduction of the size of the posterior fossa in modern humans. In normal adults, the posterior fossa comprises 27% of the total intracranial space, while in adults with Chiari Type I, it is only 21%. H. neanderthalensis had platycephalic (flattened) skulls. Some cases of Chiari are associated with platybasia (flattening of the skull base). ==History==

The history of Chiari malformation: • 1883: Cleland was the first to describe Chiari II or Arnold–Chiari malformation on his report of a child with spina bifida, hydrocephalus, and anatomical alterations of the cerebellum and brainstem. • 1891: Hans Chiari, a Viennese pathologist, described the case of a 17-year-old female with elongation of the tonsils into cone-shaped projections which accompany the medulla and are crammed into the spinal canal. • 1932: Van Houweninge Graftdijk was the first to report the surgical treatment of Chiari malformations. All patients died from surgery or postoperative complications. • 1935: Russell and Donald suggested that decompression of the spinal cord at the foramen magnum might facilitate the CSF circulation. • 1940: Gustafson and Oldberg diagnosed Chiari malformation with syringomyelia. • 1974: Bloch et al. described the tonsils position to be classified between 7 mm and 8 mm below cerebellum. • 1985: Aboulezz used MRI for discovery of extension ==Society and culture==

The condition was brought to the mainstream on the series CSI: Crime Scene Investigation in the tenth-season episode "Internal Combustion" on February 4, 2010. Notable people • Rosanne Cash – U.S. singer-songwriter; daughter of Johnny Cash • Julia Clukey – U.S. luge competitor for Team USA in 2010 Vancouver Winter Olympics • Joanna David – British television and stage actress • J. B. Holmes – U.S. professional golfer • Marissa Irwin – U.S. fashion model with Chiari secondary to Ehlers–Danlos syndrome • Bobby Jones – U.S. World Golf Hall of Fame golfer and founder of the Augusta National Golf Club • Allysa Seely – U.S. Gold Medalist at the 2016 Summer Paralympics in the paratriathlon • Leah Shapiro – U.S. drummer for the band Black Rebel Motorcycle Club • Michelle Stilwell – Canadian wheelchair racer and politician • Rachid Taha – Algerian singer • Sabre Norris – Australian skateboarder and surfer ==See also==