l-B. Dysmetria, dysdiachokinesia, intention tremor, and nystagmus are classic cerebellar signs.
In the finger-to-nose test, the patient past-points on the side of the lesion. The medial medulla
has no cerebellar pathways. In contrast, the lateral medulla has cerebellar pathways; lesions re-
sult in cerebellar ataxia and could be misdiagnosed as a cerebellar hemispheric lesion. The
globus pallidus, a basal ganglion, is atrophied in Huntington disease and in Wilson disease, and
it is damaged bilaterally by carbon monoxide intoxication.
2-A. Purkinje cells project inhibitory axons to all cerebellar nuclei: fastigial, globose, embo-
liform, and dentate. In addition, they project to all vestibular nuclei: lateral, superior, medial,
and inferior. The superior olivary nucleus is an auditory relay nucleus, and the inferior olivary
nucleus is a cerebellar relay nucleus. The arcuate nucleus is an ectopic pontine nucleus that lies
next to the pyramidal tract; its function is unknown. The ventral lateral thalamic nucleus re-
ceives input from the dentate nucleus.
3. The most common cause of the anterior ver- mis syndrome is (A) alcohol abuse (B) an abscess (C) a tumor (D) vascular occlusion (E) lead intoxication
3-A. Anterior vermis syndrome is a result of chronic alcohol abuse. Patients present with dys-
taxia of the lower limb and trunk. Posterior vermis syndrome involves the flocculonodular lobe;
it is most frequently caused by an ependymoma or a medulloblastoma. Patients have truncal dys-
taxia. Hemispheric syndrome usually is the result of a tumor (astrocytoma) or abscess; patients
have arm, leg, trunk, and gait dystaxia.
4. The most common cerebellar tumor in chil- dren is (A) astrocytoma (B) ependymoma (C) glioblastoma multiforme (D) oligodendrocytoma (E) medulloblastoma
4-A. Astrocytomas (30%) are the most common cerebellar tumors in children; they are followed by medulloblastomas (20%) and ependymomas (10%).
5-E. Medulloblastomas are derived from the external granular layer of the cerebellar cortex.
Medulloblastomas give rise to posterior vermis syndrome.
6. The inferior cerebellar peduncle contains all of the following afferent connections EXCEPT the (A) cuneocerebellar tract (B) ventral spinocerebellar tract (C) dorsal spinocerebellar tract (D) olivocerebellar tract (E) trigeminocerebellar fibers
6-B. The ventral spinocerebellar tract enters the cerebellum via the superior cerebellar peduncle.
7-E. The inferior cerebellar peduncle includes the restiform body and the juxtarestiform body.
The juxtarestiform body contains vestibulocerebellar, cerebellovestibular, and cerebelloreticular
fibers.
8-A. The vestibulocerebellum (archicerebellum) plays a role in the maintenance of posture and
balance and in the coordination of head and eye movements.
9-B. The red nucleus gives rise to the crossed rubrospinal tract, which has its primary effect on
distal muscle groups. The red nucleus is a way station in the paravermal spinocerebellar path-
way, a system dedicated to distal motor control and ongoing execution of motor acts.
10-A. In the neocerebellar pathway, the dentate nucleus projects to the contralateral ventral lat-
eral nucleus of the thalamus, which in turn projects to the motor cortex. The motor cortex gives
rise to the crossed corticopontocerebellar tract, which then modifies further cerebellar output to
the neocortex, as well as to the corticospinal and corticobulbar tracts. The neocerebellum thus
expresses itself via the corticospinal (pyramidal) and corticobulbar (corticonuclear) tracts.
11. Signs of cerebellar dysfunction include all of the following EXCEPT (A) hypotonia (B) slurred or scanning speech (C) resting static pill-rolling tremor (D) dysdiadochokinesia (E) decomposition of movement
11-C. Cerebellar signs include hypotonia, disequilibrium, muscle incoordination (dyssynergia),
and nystagmus. Intention tremor is a variation of dysmetria (inability to estimate distances cor-
rectly) and is commonly seen in lesions of the cerebellar hemispheres or their central projections.
Dysdiadochokinesia is the inability to perform rapid alternating movements. Decomposition of
movement is a breakdown of smooth muscular movement into a number of component steps. A
resting static pill-rolling tremor is seen in Parkinson disease.
12-C. The emboliform and globose nuclei are called the interposed nucleus. The fastigial nucleus
projects to the vestibular nuclei via the uncinate fasciculus (a component of the superior cere-
bellar peduncle) and via the juxtarestiform body (a component of the inferior cerebellar peduncle). The dentate nucleus, the largest of the cerebellar nuclei, gives rise to the bulk of the axons
in the superior cerebellar peduncle.
13-B. The cerebellum is attached to the brainstem by three pairs of cerebellar peduncles: Su-
perior cerebellar peduncles connect to the pons and midbrain; middle cerebellar peduncles con-
nect to the pons; and inferior cerebellar peduncles attach to the medulla.
14-D. The superior olivary nucleus is a relay nucleus of the auditory system and does not pro-
ject to the cerebellum. The inferior olivary nucleus of the medulla projects to the cerebellum via
the inferior cerebellar peduncle.
15. All of the following statements concerning the cerebellum are correct EXCEPT (A) it is derived from the alar plate (B) it develops from the rhombic lips (C) it is part of the metencephalon (D) it is part of the rhombencephalon (E) it is part of the brainstem
15-E. The cerebellum develops from the rhombic lips of the alar plates. The metencephalon (af-
terbrain) consists of the pons and cerebellum, and the rhombencephalon (hindbrain) includes the
metencephalon and the myelencephalon (medulla oblongata). The brainstem (truncus cerebri) in-
cludes the midbrain, pons, and medulla oblongata; some authorities also include the diencephalon.
16-D. The dentate nucleus is innervated by climbing and mossy fibers and receives inhibitory in-
put from the Purkinje cells of the cerebellar cortex. It gives rise to most of the fibers in the supe-
rior cerebellar peduncle (i.e., the dentatorubrothalamic tract). The dentate nucleus projects to the
ventral lateral and ventral posterolateral nuclei of the thalamus; these thalamic nuclei project to
the motor cortex. The fascia dentata (dentate gyrus) is a structure of the hippocampal formation.
17-C. Friedreich ataxia is transmitted as an autosomal recessive trait. It is the most common
of the hereditary ataxias.
18-C. With cerebello-olivary atrophy, there is no loss of cells in the substantia nigra. With olivo-
pontocerebellar atrophy, there is frequently a loss of neurons in the substantia nigra.