Initial evaluation

SYMPTOMS AND SIGNS:
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Brain tumors present in two patterns, not necessarily mutually exclusive. One consists of nonfocal symptoms of increased intracranial pressure, such as headaches, nausea, vomiting, confusion, and lethargy. The other consists of symptoms or signs of focal brain dysfunction, such as hemianopia, hemiparesis, cranial nerve palsies, or focal seizures. Such signs of focal brain dysfunction may have convincing localizing value even before an image of the brain is made by computed tomography (CT) or magnetic resonance imaging (MRI). Some tumors that arise in neurologically “silent” areas, such as the parietal or frontal association cortices, may produce only nonfocal generalized symptoms of headache, confusion, behavioral change, or, eventually, a seizure, despite growing to a considerable size. Although the capacity to reach early diagnosis by CT or MRI has greatly reduced the numbers of patients in whom symptoms of increased intracranial pressure represent initial complaints, examples still remain, especially in association with fast-growing tumors and in children. The latter are particularly likely to have tumors in the posterior fossa that tend to obstruct spinal fluid pathways earlier than do supratentorial tumors. The tempo with which a brain tumor grows also influences the presenting symptoms. Despite the fixed space within the skull (once infantile sutures have closed), the human brain possesses a remarkable capacity to make room for a slowly growing tumor. Because of this, and even allowing for the relative rapidity of growth of aggressive brain tumors, such as glioblastomas, the patient usually appears better clinically than might be expected from the degree of abnormality seen on CT or MRI scan.

FOCAL CLINICAL MANIFESTATIONS OF BRAIN TUMORS

Frontal lobe
Generalized
seizures
Focal motor
seizures (contralateral)
Expressive aphasia
(dominant side)
Behavioral changes
Dementia
Gait disorders,
incontinence
Basal ganglia
Hemiparesis (contralateral)
Movement disorders
rare
Parietal lobe
Receptive aphasia
(dominant side)
Spatial
disorientation (nondominant side)
Cortical sensory
dysfunction (contralateral)
Hemianopia (contralateral)
Occipital lobe
Hemianopia (contralateral)
Visual disturbances
(unformed)
Temporal lobe
Complex partial
(psychomotor) seizures
Generalized
seizures
Behavioral changes
Olfactory and
complex visual auras
Corpus callosum
Dementia (anterior)
Behavioral changes
(posterior)
Asymptomatic (mid)
Thalamus
Sensory loss (contralateral)
Behavioral changes
Language disorder
(dominant side)
Midbrain/pineal
Paresis of vertical
eye movements
Pupillary
abnormalities
Precocious puberty
(boys)
Sella/optic nerve/pituitary
Endocrinopathy
Bitemporal
hemianopia
Monocular visual
defects
Pons/medulla
Cranial nerve
dysfunction
Ataxia, nystagmus
Weakness, sensory
loss
Spasticity
Cerebellopontine angle
Deafness (ipsilateral)
Loss of facial
sensation (ipsilateral)
Facial weakness (ipsilateral)
Ataxia
Cerebellum
Ataxis (ipsilateral)
Nystagmus

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