Seizures and Epilepsy



Seizures and Epilepsy







A seizure reflects a transient neurologic event caused by the sudden abnormal discharge of a group of cerebral neurons. In general, seizures are a symptom of underlying brain disease—not a diagnosis. Epilepsy is the condition of repeated spontaneous and unprovoked seizures. Epilepsy has a variety of causes, both genetically determined and acquired.

Epilepsy means a state of recurring, unprecipitated seizures, and has no other implications.


TYPES OF SEIZURES

Seizures are categorized into two major types, depending on the presumed source: partial (focal) seizures or generalized seizures (Table 20.1).

In partial (focal) seizures, the initial discharge comes from a specific part of the brain. Such patients have symptoms that depend on the area of cortex involved. Thus, patients whose seizures begin with their right hand shaking or with an aura of smelling “burned candy” have a partial seizure disorder, attributable to a lesion in the frontal or temporal lobe, respectively. Partial
seizures with impairment of consciousness are known as complex partial seizures. Remember, a seizure can begin focally and then generalize. This may happen so quickly that it is impossible to see the focality clinically, and the patient can recall no aura. Nonetheless, the electroencephalogram (EEG) usually shows the focality, and historical clues (brain tumor, arteriovenous malformation [AVM]) may suggest a focal origin. Partial seizure disorders are usually secondary to local pathology (e.g., trauma, tumor, vascular lesions, or congenital abnormalities).








TABLE 20.1. Classification of Seizures















Partial (Focal)


Generalized


Simple partial


Absence


Complex partial


Myoclonic, tonic, atonic, etc.


Tonicclonic (secondary)


Tonicclonic (primary)


It is important to recognize that partial complex seizures may be manifest only by unusual and paroxysmal changes in behavior, without loss of consciousness or convulsive motor activity. This is especially true in the elderly, in which the incidence of epilepsy is increasing dramatically, and in which the manifestations of seizures can be unusual.

In generalized seizures, there are no focal sites of seizure origin. There is no aura, and there are no focal features during the seizure. Examples of generalized seizures include absence seizures (previously called petit mal) and idiopathic tonicclonic seizures (previously called grand mal). A tonicclonic seizure is a major motor seizure involving all extremities, and having tonic (stiffening) and clonic (rhythmic jerking) movements. Myoclonic jerks (rapid individual muscle movements) also may be seen in primary generalized epilepsy, often as a syndrome in teenage years, combined with absence seizures and rare tonicclonic seizures (juvenile myoclonic epilepsy of Janz).

Note: Seizures may follow unusual stress (“precipitated convulsions”) and are not considered epilepsy.

Precipitated convulsions do not equal epilepsy.

Establish whether the seizure disorder is focal or generalized.


HISTORY

Is there a history of unusual behavior, with or without loss of consciousness, which is not explained by other medical diagnoses?
Does the patient remember the event? Is there any retrograde amnesia? Is there confusion after the event?



  • Exactly how did the seizure start? Find a witness. Did the head and eyes turn? Were there other focal features? Was there an aura?


  • At what age did the seizures begin? This is important. Primary generalized seizures rarely begin before age 3 years or after age 18. “Absence seizures” that begin during adulthood, are usually complex partial seizures of temporal lobe origin.


  • Is there a family history of seizures? This may be present in both types, but is more characteristic of generalized seizure disorders.


  • Was there focal trauma at birth, or during an accident (head trauma)? Is there a history of a previous neurologic insult (e.g., stroke, encephalitis, meningitis)?


  • Does the patient have abdominal pains, nausea, dizziness, behavioral disturbances, or automatisms (frequent features of temporal lobe epilepsy)? Are there déjà vu phenomena (vivid memories of prior experiences)? Does the patient smell an odd smell for a few moments (a common symptom of seizures from the mesial temporal lobe)?


  • Have there been brief staring spells not followed by postictal confusion, or fatigue (absence seizures)?


EXAMINATION



  • Look for post-ictal paralysis (Todd paralysis) by checking for asymmetry of reflexes, hemiparesis, an upgoing toe, or hemiparetic posturing of a leg.


  • Look for asymmetry of fingernail, toe, and limb size (a clue to early damage to the contralateral hemisphere).


  • Absence seizures (a primary generalized seizure of childhood) can be precipitated by hyperventilation. Have the patient breathe deeply for 5 minutes, and watch for a brief, transient cessation of activity and “glassy stare.”


  • Examine the skin carefully. Neurocutaneous disorders such as neurofibromatosis, tuberous sclerosis, and Sturge-Weber disease may present with seizures.


LABORATORY AIDS IN DIAGNOSIS



  • In addition to baseline laboratory studies (including glucose, blood urea nitrogen, calcium, sodium), perform an EEG,
    a magnetic resonance imaging (MRI) scan, or computed tomography (CT) scan for any unexplained first seizure. An MRI is more sensitive than a CT scan in locating the etiology in focal seizures.


  • Obtain a sleep-deprived EEG if a focal seizure disorder is suspected. Frequently, it will bring out the spike focus. In some cases, the spike focus can be seen only with special (e.g., anterior temporal or sphenoidal) EEG leads.


  • MRI is accurate in detecting small tumors, focal gliosis, cortical dysgenesis, and mesial temporal sclerosis, all of which may cause partial seizures. Coronal thin slices through the temporal lobes using fluid-attenuation inversion recovery (FLAIR) sequences increase the yield of MRI in focal epilepsies.

Many patients with epilepsy do not have structural lesions on imaging. This in no way stands against the diagnosis of epilepsy.


WHAT ETIOLOGIC FACTORS ARE INVOLVED?

Drug withdrawal (from alcohol, barbiturates, and other sedatives) is a common cause of seizures in adults. Alcohol withdrawal seizures occur 12 to 48 hours after the cessation of drinking (see Chapter 27). Alcoholics with post-traumatic epilepsy secondary to frequent falls may have an exacerbation of seizures when intoxicated.

Exacerbation of a known seizure disorder is common. Persons with a controlled seizure disorder, who come to the hospital because of a recurrence, usually have:

Oct 20, 2016 | Posted by in NEUROLOGY | Comments Off on Seizures and Epilepsy

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