Q 1.24. Brainstem Syndromes: Mesencephalon

Q 1.24. Brainstem Syndromes: Mesencephalon

Mesencephalon (Midbrain):

    • The mesencephalon is the smallest part of the brainstem, located cranially.
    • Embryologically, it develops from the neural ectoderm and forms a critical connection between the cerebrum, cerebellum, and spinal cord.

 

Here’s an overview of midbrain structures and the symptoms observed with lesions in these areas:

1. Tectum:
– Comprises the superior and inferior colliculi.
– Lesions can lead to visual and auditory deficits.
– Damage to the superior colliculus can cause impaired visual reflexes, such as difficulty tracking moving objects or saccadic eye movements.
– Damage to the inferior colliculus can result in auditory processing deficits, affecting the ability to localize sound sources.

2. Tegmentum:
– Includes nuclei and fiber tracts involved in motor and sensory functions, as well as arousal and consciousness.
– Lesions in this area can lead to various motor and sensory deficits, depending on the structures affected.
– Damage to the red nucleus can result in contralateral tremors and movement disorders.
– Lesions affecting the substantia nigra can lead to Parkinsonian symptoms.
– Damage to the medial longitudinal fasciculus (MLF) can cause internuclear ophthalmoplegia (INO), characterized by impaired adduction of the ipsilateral eye on horizontal gaze.

3. Cerebral Peduncles:
– Contain descending motor fibers such as the corticospinal and corticobulbar tracts.
– Lesions can lead to contralateral motor deficits.
– Damage to the corticospinal tract can result in contralateral hemiparesis or hemiplegia, as seen in Weber syndrome.

4. Crus Cerebri:
– Houses motor and sensory fibers traveling to and from the cerebrum.
– Lesions can lead to various motor and sensory deficits, depending on the structures affected.
– Damage to the oculomotor nerve (CN III) can result in ipsilateral ptosis, diplopia, and impaired extraocular movements, as seen in Weber, Benedict, and Claude syndromes.
– Compression of the oculomotor nerve can also cause dilation of the pupil (mydriasis) and loss of pupillary light reflex.

 

Some of the wellknown mesencephalon syndromes are:

 

Weber Syndrome:

  •    Characterized by:

     – Ipsilateral oculomotor nerve (CN III) palsy.

     – Contralateral hemiparesis or hemiplegia due to involvement of the cerebral peduncle.

  •    Often caused by:

     – Occlusion of the posterior cerebral artery.

 

Internuclear Ophthalmoplegia (INO):

  •    Characterized by:

     – Impaired adduction of the ipsilateral eye on attempted horizontal gaze.

     – Convergence usually unaffected.

  •    Typically caused by:

     – Lesions affecting the medial longitudinal fasciculus (MLF), often due to multiple sclerosis.

 

Benedict Syndrome:

  •    Characterized by:

     – Ipsilateral oculomotor nerve (CN III) palsy.

     – Contralateral cerebellar ataxia.

  •    Resulting from:

     – Lesions affecting the midbrain tegmentum, often due to vascular events or tumors.

 

Claude Syndrome:

  •    Characterized by:

     – Ipsilateral oculomotor nerve (CN III) palsy.

     – Contralateral ataxia and tremor.

  •    Usually resulting from:

     – Lesions affecting the tegmentum of the midbrain, commonly due to vascular pathology.

 

Parinaud Syndrome:

  •    Characterized by:

     – Vertical gaze palsy, often with an upward gaze palsy.

     – Convergence-retraction nystagmus.

     – Light-near dissociation of pupils.

  •    Typically due to:

     – Compression or damage to the dorsal midbrain, often by tumors or pineal gland masses.

 

________________________

Remember the Rule of 4:

      • 4 structures in the midbrain (CN III, IV, V, VI).
      • 4 structures in the pons (CN V, VI, VII, VIII).
      • 4 structures in the medulla (CN IX, X, XI, XII).
    • This simplified approach helps localize the affected artery and understand the distinguishing features of each syndrome.

 

References:

(1)ncbi.nlm.nih.gov

(2)researchgate.net

(3)radiopaedia.org

Одобрено от Dr. Petya Stefanova

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