Aphasia

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Aphasia
ICD-10	F80.0-F80.2, R47.0
ICD-9	315.31, 784.3
DiseasesDB	4024
MedlinePlus	003204
MeSH	D001037

Template:Search infobox Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor(s)-In-Chief: Leah Biller

Overview

Aphasia (or aphemia) is a loss of the ability to produce and/or comprehend language, due to injury to brain areas specialized for these functions. It is not a result of deficits in sensory, intellect, or psychiatric functioning. It is also not due to muscle weakness or a cognitive disorder.

Depending on the area and extent of the damage, someone suffering from aphasia may be able to speak but not write, or vice versa, or display any of a wide variety of other deficiencies in language comprehension and production, such as being able to sing but not speak. Aphasia may co-occur with speech disorders such as dysarthria or apraxia of speech, which also result from brain damage.

Causes

Usually, aphasias are a result of damage (lesions) to the language centres of the brain (like Broca's area). These areas are almost always located in the left hemisphere, and in most people this is where the ability to produce and comprehend language is found. However, in a very small number of people language ability is found in the right hemisphere. In either case, damage to these language areas can be caused by a stroke, traumatic brain injury, or other head injury. Aphasia may also develop slowly, as in the case of a brain tumor or progressively neurological disease. It may also be caused by a sudden hemorrhagic event within the brain.

Causes of Aphasia in Alphabetical Order

• Alexia (disorder)
• Alzheimer's dementia
• Aortic Arch Syndrome
• Arcuate fasciculus damage
• Brain abscess
• Brain tumor
• Cerebral arteriovenous malformation
• Cerebral atrophy
• Cerebral venous sinus thrombosis
• Cerebrovascular accident
• Dementia
• Dissociative state
• Frontotemporal dementia
• Frontotemporal lobar degeneration
• Gerstmann syndrome
• Hemispatial neglect
• Hemorrhage
• Herpes Encephalitis
• Hypoglycemia
• Insulin shock therapy
• Intracranial space-occupying lesion
• Landau-Kleffner syndrome
• Malignant Astrocytomas
• MASA syndrome
• Migraine
• Motor neuron disease
• Multi-infarct dementia
• Multiple sclerosis
• Nonconvulsive status epilepticus
• Pick's disease
• Postconcussion syndrome
• Rasmussen's encephalitis
• Santonin
• Schilder's disease
• Sedative-hypnotic drug intoxication
• Semantic dementia
• Senile dementia
• Stroke
• Subdural hematoma
• Temporal lobe abscess
• Temporal lobe atrophy
• Tertiary syphilis
• Thromboangitis obliterans
• Transient ischemic attack
• Trauma
• Traumatic brain injury
• Wernicke syndrome
• Wernicke's encephalopathy

Prognosis

The prognosis of those with aphasia varies widely, and is dependent upon age of the patient, site and size of lesion, and type of aphasia.

Diagnosis

Aphasia can be assessed in a variety of ways, from quick clinical screening at the bedside to several-hour-long batteries of tasks that examine the key components of language and communication.

Symptoms

Any of the following can be considered symptoms of aphasia:

• Inability to comprehend language
• Inability to pronounce, not due to muscle paralysis or weakness
• Inability to speak spontaneously
• Inability to form words
• Inability to name objects
• Poor enunciation
• Excessive creation and use of personal neologisms
• Inability to repeat a phrase
• Persistent repetition of phrases
• Paraphasia (substituting letters, syllables or words)
• Agrammatism (inability to speak in a grammatically correct fashion)
• Dysprosody (alterations in inflexion, stress, and rhythm)
• Uncompleted sentences
• Inability to read
• Inability to write

Laboratory Findings

The following laboratory tests are suggested:

• Complete blood count (CBC)
• Calcium
• Glucose
• Blood urea nitrogen (BUN)/creatinine
• Vitamin B12
• Rapid plasma reagin (RPR)

Electrolyte and Biomarker Studies

• Electrolytes

MRI and CT

• Cerebral imaging critical.
• MRI has highest specificity and sensitivity

Other Imaging Findings

• Electroencephalogram (EEG)

Other Diagnostic Studies

• Psychometric testing (dementia)
• Toxicology screen
• Cerebrospinal fluid (CSF) analysis

Classification of aphasia

Classifying the different subtypes of aphasia is difficult and has led to disagreements among experts. The locationist model is the original model, but modern anatomical techniques and analyses have shown that precise connections between brain regions and symptom classification don't exist. The neural organization of language is complicated; language is a comprehensive and complex behavior and it makes sense that it isn't the product of some small, circumscribed region of the brain.
No classification of patients in subtypes and groups of subtypes is adequate. Only about 60% of patients will fit in a classification scheme such as fluent/nonfluent/pure aphasias. There is a huge variation among patients with the same diagnosis, and aphasias can be highly selective. For instance, patients with naming deficits (anomic aphasia) might show an inability only for naming buildings, or people, or colors.

The locationist model

Cortex

The locationist model attempts to classify the aphasia by major characteristics and then link these to areas of the brain in which the damage has been caused. The initial two categories here were devised by early neurologists working in the field, namely Paul Broca and Carl Wernicke. Other researchers have added to the model, resulting in it often being referred to as the "Boston-Neoclassical Model". The most prominent writers on this topic have been Howard Goodglass and Edith Kaplan.

• Individuals with Broca's aphasia (also termed expressive aphasia) were once thought to have ventral temporal damage though more recent work by Nina Dronkers using imaging and 'lesion analysis' has revealed that patients with Broca's Aphasia have lesions to the medial insular cortex. Broca missed these lesions because his studies did not disect the brains of diseased patients so only the more temporal damage was visible. Individuals with Broca's aphasia often have right-sided weakness or paralysis of the arm and leg because the frontal lobe is also important for body movement.

• In contrast to Broca's aphasia, damage to the temporal lobe may result in a fluent aphasia that is called Wernicke's aphasia (also termed sensory aphasia). These individuals usually have no body weakness because their brain injury is not near the parts of the brain that control movement.

• Working from Wernicke's model of aphasia, Ludwig Lichtheim proposed five other types of aphasia but these were not tested against real patients until modern imaging made more indepth studies available. The other five types of aphasia in the locationist model are:

1. Pure word deafness
2. Conduction aphasia
3. Apraxia of speech, which is now considered a separate disorder in itself.
4. Transcortical motor aphasia
5. Transcortical sensory aphasia

• Anomia is another type of aphasia proposed under what is commonly known as the Boston-Neoclassical model, which is essentially a difficulty with naming. A final type of aphasia, global aphasia, results from damage to extensive portions of the language areas of the brain.

Fluent, non-fluent and "pure" aphasias

The different types of aphasia can be divided into three categories: fluent, non-fluent and "pure" aphasias.

• Fluent aphasias, also called receptive aphasias, are impairments related mostly to the input or reception of language, with difficulties either in auditory verbal comprehension or in the repetition of words, phrases, or sentences spoken by others. Speech is easy and fluent, but there are difficulties related to the output of language as well, such as paraphasia. Examples of fluent aphasias are: Wernicke's aphasia, Transcortical sensory aphasia, Conduction aphasia, Anomic aphasia

• Nonfluent aphasias, also called expressive aphasias are difficulties in articulating, but in most cases there is relatively good auditory verbal comprehension. Examples of nonfluent aphasias are: Broca's aphasia, Transcortical motor aphasia, Global aphasia

• "Pure" aphasias are selective impairments in reading, writing, or the recognition of words. These disorders may be quite selective. For example, a person is able to read but not write, or is able to write but not read. Examples of pure aphasias are: Alexia, Agraphia, Pure word deafness

The cognitive neuropsychological model

The cognitive neuropsychological model builds on cognitive neuropsychology. It assumes that language processing can be broken down into a number of modules, each of which has a specific function. Hence there is a module which recognises phonemes as they are spoken and a module which stores formulated phonemes before they are spoken. Use of this model clinically involves conducting a battery of assessments (usually from the PALPA), each of which tests one or a number of these modules. Once a diagnosis is reached as to where the impairment lies, therapy can proceed to treat the individual module.

A few less common subtypes include:

• Subcortical motor aphasia
• Subcortical sensory aphasia
• Mixed transcortical aphasia
• Acquired eleptiform aphasia (Landau Kleffner Syndrome)

A combination of subtypes is possible.

Primary and secondary aphasia

Aphasia can be divided into primary and secondary aphasia.

• Primary aphasia is due to problems with language-processing mechanisms.
• Secondary aphasia is the result of other problems, like memory impairments, attention disorders, or perceptual problems.

Types of Aphasia

• Anomic aphasia
• Conduction aphasia
• Expressive (Broca's) aphasia
• Receptive (Wernicke's) aphasia
• Transcortical motor aphasia
• Transcortical sensory aphasia

Treatment

• Speech therapy
• Correction of underlying etiology

Acute Pharmacotherapies

• IV acyclovir (viral encephalitis)
• Acetylcholinesterase inhibitors (dementia)
• Anticoagulation (embolic stroke)
• Antiplatelet therapy (thrombotic stroke)
• IV lorazepam, anticonvulsants (status epilepticus)
• IV or oral benzodiazepines (dissociative state)

See also

• Speech disorder
• Dysnomia disorder

Sources

Academic references

• R. Chapey (Ed.) (2001). Language Intervention Strategies in Aphasia and Related Neurogenic Communication Disorders (Fourth Edition). Philadelphia: Lippincott, Williams & Wilkins.
• Goodglass, H. & Kaplan, E. (1972). Assessment of Aphasia and Related Disorders. Philadelphia: Lea and Febinger.
• Kay, J., Lesser, R., & Coltheart, M. (1992). Psycholinguistic Assessments of Language Processing in Aphasia (PALPA). Hove: Erlbaum.
• Spreen, O. & Risser, A.H. (2003). Assessment of Aphasia. New York: Oxford University Press.

Personal experiences of aphasia

• Hale, S (2003), The Man Who Lost His Language, Penguin.
• Paul E. Berger and Stephanie Mensh, How to Conquer the World With One Hand...And an Attitude, 2nd Ed., ISBN 0-9668378-7-8
• Cindy Greatrex (2005) Aphasia in the Deaf Community.
• Dardick, Geeta (1991), Prisoner of Silence, Reader's Digest, June issue

References

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