Symptoms and signs may include gait impairment, visual blurring due to nystagmus, unclear (“scanning”) speech, hand incoordination, and tremor with movement. Differential diagnosis: Unsteady gait associated with vertigo from vestibular nerve or labyrinthine disease can resemble gait instability of cerebellar disease but produces a perception of movement, dizziness, or light-headedness. Sensory disturbances also can simulate cerebellar disease; with sensory ataxia, imbalance dramatically worsens when visual input is removed (Romberg sign). Bilateral proximal leg weakness also can rarely mimic cerebellar ataxia.
APPROACH TO THE PATIENT: Ataxia
Causes are best grouped by determining whether ataxia is symmetric or focal and by the time course (Table 184-1). Also important to distinguish whether ataxia is present in isolation or is part of a multisystem neurologic disorder. Acute symmetric ataxia is usually due to medications, toxins including alcohol, viral infection, or a postinfectious syndrome (especially varicella). Subacute or chronic symmetric ataxia can result from hypothyroidism, vitamin deficiencies, infections (Lyme disease, tabes dorsalis, prions), alcohol, other toxins, or an inherited condition (see below). An immune-mediated progressive ataxia is associated with antigliadin antibodies; biopsy of the small intestine may reveal villous atrophy of gluten enteropathy. Elevated serum anti–glutamic acid decarboxylase (GAD) antibodies have been associated with a progressive ataxic syndrome affecting speech and gait. Progressive nonfamilial cerebellar ataxia after age 45 suggests a paraneoplastic syndrome, either subacute cortical cerebellar degeneration (ovarian, breast, lung, Hodgkin’s) or opsoclonus-myoclonus (neuroblastoma, breast, lung).
Unilateral ataxia suggests a focal lesion in the ipsilateral cerebellar hemisphere or its connections. An important cause of acute unilateral ataxia is stroke. Mass effect from cerebellar hemorrhage or swelling from cerebellar infarction can compress brainstem structures, producing altered consciousness and ipsilateral pontine signs (small pupils, sixth or seventh nerve palsies); limb ataxia may not be prominent. Other diseases producing asymmetric or unilateral ataxia include tumors, multiple sclerosis, progressive multifocal leukoencephalopathy (immunodeficiency states), and congenital malformations.
TABLE 184-1ETIOLOGY OF CEREBELLAR ATAXIA |Favorite Table|Download (.pdf) TABLE 184-1ETIOLOGY OF CEREBELLAR ATAXIA
|Symmetric and Progressive Signs ||Focal and Ipsilateral Cerebellar Signs |
|Acute (Hours to Days) ||Subacute (Days to Weeks) ||Chronic (Months to Years) ||Acute (Hours to Days) ||Subacute (Days to Weeks) ||Chronic (Months to Years) |
Intoxication: alcohol, lithium, phenytoin, barbiturates (positive history and toxicology screen)
Acute viral cerebellitis (CSF supportive of acute viral infection)
Intoxication: mercury, solvents, gasoline, glue; cytotoxic chemotherapeutic, hemotherapeutic drugs
Alcoholic-nutritional (vitamin B1 and B12 deficiency)
Antigliadin antibody syndrome
Tabes dorsalis (tertiary syphilis)
Vascular: cerebellar infarction, hemorrhage, or subdural hematoma
Infectious: cerebellar abscess (mass lesion on MRI/CT, history in support of lesion)
Neoplastic: cerebellar glioma or metastatic tumor (positive for neoplasm on MRI/CT)
Demyelinating: multiple sclerosis (history, CSF, and MRI are consistent)
AIDS-related multifocal leukoencephalopathy (positive HIV test and CD4+ cell count for AIDS)
Stable gliosis secondary to vascular lesion or demyelinating plaque (stable lesion on MRI/CT ...