| Rolandic epilepsy | |
|---|---|
| Classification and external resources | |
Diagram showing the central sulcus of the brain. |
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| ICD-10 | G40.0 |
| OMIM | 117100 |
| DiseasesDB | 33998 |
| eMedicine | neuro/641 |
| MeSH | D019305 |
In neurology and pediatrics, benign rolandic epilepsy or benign (childhood) epilepsy with centrotemporal (EEG) spikes (also known as sylvian seizures) is the most common epilepsy syndrome in childhood.[1] Most children will outgrow the syndrome (it starts around the age of 3-13 with a peak around 8–9 years and stops around age 14-18), hence the label benign.[2][3] The seizures start around the central sulcus of the brain (also called the centrotemporal area, located around the Rolandic fissure, after Luigi Rolando).[4]
Contents |
Benign rolandic epilepsy is characterized by either simple partial seizures involving the mouth and face or generalized tonic-clonic seizures. There can be one-sided somatosensory manifestations such as tingling (paresthesia) of one side of the tongue, speech arrest (anarthria), gurgling or grunting noises or drooling.[2][3] Seizures tend to occur more often during the night.[2] Psychic manifestations, auras and automatisms are lacking. The seizure frequency is often low. These children usually have normal intelligence and development.[2] Atypical features however, such as developmental delay or daytime seizures, are common.[3] There is increasing data that a subset of children with atypical EEG or clinical features appear to be at risk for cognitive and behavioral problems, thus in some children the diagnosis may not be as "benign" as previously thought. Most children however appear to do well, typically outgrowing their seizures by adolescence.
The diagnosis can be confirmed when the characteristic centrotemporal spikes are seen on electroencephalography (EEG).[5] Typically, high-voltage spikes followed by slow waves are seen.[6] Given the nocturnal activity, a sleep EEG can often be helpful. Technically, the label "benign" can only be confirmed if the child's development continues to be normal during follow-up.[3] Neuroimaging, usually with an MRI scan, is only advised for cases with atypical presentation or atypical findings on clinical examination or EEG.
Given the benign nature of the condition and the low seizure frequency, treatment is often unnecessary. If treatment is warranted or preferred by the child and its family, antiepileptic drugs can usually control the seizures easily.[2] Carbamazepine is the most frequently used first-line drug, but many other antiepileptic drugs, including valproate, phenytoin, gabapentin, levetiracetam and sultiame have been found effective as well.[3] Bedtime dosing is advised by some.[7] Treatment can be short and drugs can almost certainly be discontinued after two years without seizures and with normal EEG findings, perhaps even earlier.[3]
Benign epilepsy with centrotemporal spikes is thought to be a genetic disorder. An autosomal dominant inheritance with age dependency and variable penetrance has been reported, although not all studies support this theory.[3][8][9] Linkage studies have pointed to a possible susceptibility region on chromosome 15q14, in the vicinity of the alpha-7 subunit of the acetylcholine receptor.[10] Most studies show a slight male predominance.[3] Because of the benign course and age-specific occurrence, it is thought to represent a hereditary impairment of brain maturation.[3]
An association with ELP4 has been identified.[11]
The disorder should be differentiated from several other conditions, especially centrotemporal spikes without seizures, centrotemporal spikes with local brain pathology, central spikes in Rett syndrome and fragile X syndrome, malignant rolandic epilepsy, temporal lobe epilepsy and Landau-Kleffner syndrome.
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