Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis (81 page)

BOOK: Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis
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References
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HUNTINGTON DISEASE

Huntington disease (HD) is a neurodegenerative disease presenting with choreiform movements, psychiatric disorder, and dementia (see HD in the section on Disorders of Movement).

DISORDERS OF ALTERED MENTAL STATE
COMA AND STUPOR
   Definition

Coma is defined as unconsciousness lasting for more than 6 hours. There is no response to external stimuli, including pain and no voluntary movements. Stupor is defined as a decreased level of consciousness in which there is only response to pain.

   Clinical Presentation

Patients with coma or stupor are poorly or nonresponsive to external stimuli. The causes are many and can be divided into several etiologic categories (see “Causes” below). The goal of diagnostic testing is to identify treatable conditions including infection, metabolic abnormalities, seizures, intoxications/overdose, and surgical lesions as rapidly as possible. Diagnosis is made on physical and neurologic examination, history, neuroimaging, and laboratory testing.
1,2

   Causes
Poisons, Drugs, or Toxins
   Sedatives (especially alcohol, barbiturates)
   Enzyme inhibitors (especially salicylates, heavy metals, organic phosphates, cyanide)
   Other (e.g., paraldehyde, methyl alcohol, ethylene glycol)

Cerebral Disorders

   Brain contusion, hemorrhage, infarction, seizure, or aneurysm
   Brain mass (e.g., tumor, hematoma, abscess, parasites)
   Subdural or epidural hematoma
   Venous sinus occlusion

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