Difference between revisions of "Forebrain Disease"
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+ | ==The Forebrain== | ||
+ | |||
+ | * The nervous system can be classified functionally to: | ||
+ | *# The intercranial structures | ||
+ | *# The spinal cord | ||
+ | *# The peripheral nervous system. | ||
+ | * The intercranial structures can be further divided into the '''rostrotentorial''' and '''caudotentorial''' structures. | ||
+ | ** The rostrotentorial structures consist of the cerebral hemispheres, basal nuclei, diencephalon and the rostral portion of the midbrain. | ||
+ | *** Collectively, these are the forebrain. | ||
+ | * The forebrain is responsible for many functions associated with or requiring consciousness. | ||
+ | |||
+ | ==Clinical Signs== | ||
+ | |||
+ | ===Seizures=== | ||
+ | |||
+ | * Seizures are a classical sign of rostrotentorial disease. | ||
+ | |||
+ | ===Altered Mentality/ Behaviour=== | ||
+ | |||
+ | * The forebrain contains significant components of the limbic system, which are responsible for emotion. | ||
+ | ** Intercranial disease may therefore give rise to abnormal behaviour and aggression. | ||
+ | |||
+ | ===Circling, Head Pressing, Compulsive Walking=== | ||
+ | |||
+ | * These behaviours are associated with unilateral rostrotentorial disease. | ||
+ | * There is a tendency to circle '''towards''' the side of the lesion. | ||
+ | |||
+ | ===Head Aversion=== | ||
+ | |||
+ | * Head aversion is also known as head turn. | ||
+ | * Turn is usually towards the side of a unilateral lesion. | ||
+ | |||
+ | ===Menace Deficit=== | ||
+ | |||
+ | * There may be a deficit in the menace response on the opposite side to a unilateral lesion. | ||
+ | ** However, the pupillary light reflex (testing optic nerve function) and facial nerve function are found to be normal. | ||
+ | * The lack of a contralateral menace response is associated with poor or absent vision. | ||
+ | ** The menace reflex is a learned response, and requires forebrain processing of visual information. | ||
+ | ** The sign is contralateral because there is significant decussation of the visual fibres at the optic chiasm in animals. | ||
+ | * There may also be a reduction in the medial visual field in the eye ipsilateral to the lesion. | ||
+ | ** This combination of visual field abnormalities is known as '''hemianopia'''. | ||
+ | |||
+ | ===Facial Sensation Deficit=== | ||
+ | |||
+ | * There may be a deficit in facial sensation on the side contralateral to a unilateral lesion. | ||
+ | ** This is because CN V sends facial sensory signals to the opposite parietal cortex via the thalamus. | ||
+ | |||
+ | ===Hemiparesis=== | ||
+ | |||
+ | * Hemiparesis may be a sign of forebrain disease. | ||
+ | * Many tracts cross at various levels in the CNS, however functional crossover occurs at the level of the causal mesencephalon and rostral pons. | ||
+ | ** Unilateral lesions rostral to this level give contralateral hemipareis. | ||
+ | ** Unilateral lesions caudal to this level give ipsilateral hemiparesis. | ||
+ | |||
+ | ==Differential Diagnosis== | ||
+ | |||
+ | * Remember that the age and breed of the animal are important. | ||
+ | ** Animals present with congenital abnormalities within their first year of life. | ||
+ | ** Young animals are also more predisposed to: | ||
+ | *** Infections - due to their immature immune systems and lack of vaccinations. | ||
+ | *** Intoxications - due to their innate curiosity and propensity to explore with their mouths. | ||
+ | *** Traumatic injury - due to both their curiosity and lack of road sense. | ||
+ | ** Geriatric animals tend to suffer the same kind of neurological problems as other adult animals. | ||
+ | *** Infectious, inflammatory and metabolic disorders. | ||
+ | ** Elderly animals are more likely to suffer from: | ||
+ | *** Neoplasi | ||
+ | *** Vascular problems | ||
+ | *** Degenerative disorders | ||
+ | * It must be determined whether the suspected lesion is due to a systemic disease, or to a structural change in the intracranial nervous system. | ||
+ | ** Structural change can be detected by CT or MRI scanning. | ||
+ | * The following causes must be considered and eliminated. | ||
+ | |||
+ | ===Common Diseases Affecting the Forebrain=== | ||
+ | |||
+ | ====Degenerative Diseases==== | ||
+ | |||
+ | * Storage diseases | ||
+ | * Cognitive dysfunction syndrome | ||
+ | |||
+ | ====Anomalies==== | ||
+ | |||
+ | * Hydrocephalus | ||
+ | * Hydraencephaly | ||
+ | * Lissencephaly | ||
+ | |||
+ | ====Metabolic Diseases==== | ||
+ | |||
+ | * Hepatic encephalopathy | ||
+ | ** Most commonly seen with congential liver shunts or with sever liver failure. | ||
+ | * Renal encephalopathy | ||
+ | * Pancreatic disease | ||
+ | * Glucose abnormalities | ||
+ | ** Insulinoma | ||
+ | ** Diabetes Mellitus | ||
+ | * Hypo- and hyper-thyroidism | ||
+ | * Hypoxia, for example due to: | ||
+ | ** Anaemia | ||
+ | ** Cariopulmonary disease | ||
+ | ** Severe URT obstruction | ||
+ | * Hypertension | ||
+ | * Ion inbalances | ||
+ | ** Hypocalcaemia | ||
+ | ** Hypokalaemia | ||
+ | *** For example in chronic renal failure or hyperaldosteronism | ||
+ | ** Hypophosphataemia | ||
+ | ** Hypomagnesaemia | ||
+ | *** E.g. in hepatic lipidosis or re-feeding syndrome. | ||
+ | |||
+ | ====Neoplasia==== | ||
+ | |||
+ | * Primary brain tumours | ||
+ | * Metastatic tumours | ||
+ | * Local extension of tumours | ||
+ | |||
+ | ====Nutrtional Conditions==== | ||
+ | |||
+ | * Thiamine deficiency | ||
+ | |||
+ | ====Infectious Causes==== | ||
+ | |||
+ | * Canine distemper | ||
+ | * FIP | ||
+ | * Toxoplasmosis | ||
+ | * Fungal disease | ||
+ | * Rickettsial diseases | ||
+ | * Rock Mountain spotted fever | ||
+ | * Ehrlichia | ||
+ | * Bacterial infections | ||
+ | * Parasitism | ||
+ | |||
+ | ====Trauma==== | ||
+ | |||
+ | * Head trauma | ||
+ | |||
+ | ====Toxicity==== | ||
+ | |||
+ | * Metranidazole | ||
+ | * Lead | ||
+ | |||
+ | ====Vascular==== | ||
+ | |||
+ | * Arteriovenous malformation | ||
+ | * Infarction | ||
+ | * Feline ischaemic encephalopathy | ||
+ | * Haemorrhage | ||
+ | * Hypertension | ||
+ | |||
+ | ==Diagnosis== | ||
+ | |||
+ | * Diagnosis must encompass the following: | ||
+ | |||
+ | ===History=== | ||
+ | |||
+ | * Aside from the normal history, there are several very important questions to be asked: | ||
+ | ** Has there been any possible exposure to toxins or trauma? | ||
+ | ** What is the animal's diet? | ||
+ | ** Are the litter mates normal? | ||
+ | ** Are there any specific clinical signs that may relate to a particular diagnosis? | ||
+ | ** E.g. hypersalivation - commonly seens in young animals with portosystemic [[Liver - Anatomy & Physiology|liver]] shunts. | ||
+ | |||
+ | ===Physical Examinations=== | ||
+ | |||
+ | * Check for signs of systemic disease. | ||
+ | ** Ocular changes with FIP, toxoplasmosis, FeLV or lysosomal storage diseases. | ||
+ | ** Ascites with with FIP, liver or cardiac disease. | ||
+ | |||
+ | ===Neurological Examination=== | ||
+ | |||
+ | * This should include CN examination, postural reactions, spinal reflexes and sensory examination. | ||
+ | |||
+ | ===Blood and Urine Tests=== | ||
+ | |||
+ | * Blood tests should include haematology and serum biochemistry. | ||
+ | * These are particularly helpful in the diagnosis of many systemic and especially metabloic conditions. | ||
+ | |||
+ | ===Infectious Disease Tests=== | ||
+ | |||
+ | * E.g. FeLV and FIV, toxoplasma IgM and IgG tests. | ||
+ | |||
+ | ===CSF Analysis=== | ||
+ | |||
+ | * Particularly useful in the diagnosis of: | ||
+ | ** Inflammatory diseases | ||
+ | *** E.g. FIP | ||
+ | ** Lymphoma | ||
+ | |||
+ | ===Imaging=== | ||
+ | |||
+ | * Radiographs of the chest and abdomen | ||
+ | * Abdominal ultrasonography | ||
+ | * MRI or CT scans | ||
+ | ** Examine the structure of the brain and determine presence or absence of inflammation or neoplasia. |
Revision as of 10:57, 18 August 2008
|
The Forebrain
- The nervous system can be classified functionally to:
- The intercranial structures
- The spinal cord
- The peripheral nervous system.
- The intercranial structures can be further divided into the rostrotentorial and caudotentorial structures.
- The rostrotentorial structures consist of the cerebral hemispheres, basal nuclei, diencephalon and the rostral portion of the midbrain.
- Collectively, these are the forebrain.
- The rostrotentorial structures consist of the cerebral hemispheres, basal nuclei, diencephalon and the rostral portion of the midbrain.
- The forebrain is responsible for many functions associated with or requiring consciousness.
Clinical Signs
Seizures
- Seizures are a classical sign of rostrotentorial disease.
Altered Mentality/ Behaviour
- The forebrain contains significant components of the limbic system, which are responsible for emotion.
- Intercranial disease may therefore give rise to abnormal behaviour and aggression.
Circling, Head Pressing, Compulsive Walking
- These behaviours are associated with unilateral rostrotentorial disease.
- There is a tendency to circle towards the side of the lesion.
Head Aversion
- Head aversion is also known as head turn.
- Turn is usually towards the side of a unilateral lesion.
Menace Deficit
- There may be a deficit in the menace response on the opposite side to a unilateral lesion.
- However, the pupillary light reflex (testing optic nerve function) and facial nerve function are found to be normal.
- The lack of a contralateral menace response is associated with poor or absent vision.
- The menace reflex is a learned response, and requires forebrain processing of visual information.
- The sign is contralateral because there is significant decussation of the visual fibres at the optic chiasm in animals.
- There may also be a reduction in the medial visual field in the eye ipsilateral to the lesion.
- This combination of visual field abnormalities is known as hemianopia.
Facial Sensation Deficit
- There may be a deficit in facial sensation on the side contralateral to a unilateral lesion.
- This is because CN V sends facial sensory signals to the opposite parietal cortex via the thalamus.
Hemiparesis
- Hemiparesis may be a sign of forebrain disease.
- Many tracts cross at various levels in the CNS, however functional crossover occurs at the level of the causal mesencephalon and rostral pons.
- Unilateral lesions rostral to this level give contralateral hemipareis.
- Unilateral lesions caudal to this level give ipsilateral hemiparesis.
Differential Diagnosis
- Remember that the age and breed of the animal are important.
- Animals present with congenital abnormalities within their first year of life.
- Young animals are also more predisposed to:
- Infections - due to their immature immune systems and lack of vaccinations.
- Intoxications - due to their innate curiosity and propensity to explore with their mouths.
- Traumatic injury - due to both their curiosity and lack of road sense.
- Geriatric animals tend to suffer the same kind of neurological problems as other adult animals.
- Infectious, inflammatory and metabolic disorders.
- Elderly animals are more likely to suffer from:
- Neoplasi
- Vascular problems
- Degenerative disorders
- It must be determined whether the suspected lesion is due to a systemic disease, or to a structural change in the intracranial nervous system.
- Structural change can be detected by CT or MRI scanning.
- The following causes must be considered and eliminated.
Common Diseases Affecting the Forebrain
Degenerative Diseases
- Storage diseases
- Cognitive dysfunction syndrome
Anomalies
- Hydrocephalus
- Hydraencephaly
- Lissencephaly
Metabolic Diseases
- Hepatic encephalopathy
- Most commonly seen with congential liver shunts or with sever liver failure.
- Renal encephalopathy
- Pancreatic disease
- Glucose abnormalities
- Insulinoma
- Diabetes Mellitus
- Hypo- and hyper-thyroidism
- Hypoxia, for example due to:
- Anaemia
- Cariopulmonary disease
- Severe URT obstruction
- Hypertension
- Ion inbalances
- Hypocalcaemia
- Hypokalaemia
- For example in chronic renal failure or hyperaldosteronism
- Hypophosphataemia
- Hypomagnesaemia
- E.g. in hepatic lipidosis or re-feeding syndrome.
Neoplasia
- Primary brain tumours
- Metastatic tumours
- Local extension of tumours
Nutrtional Conditions
- Thiamine deficiency
Infectious Causes
- Canine distemper
- FIP
- Toxoplasmosis
- Fungal disease
- Rickettsial diseases
- Rock Mountain spotted fever
- Ehrlichia
- Bacterial infections
- Parasitism
Trauma
- Head trauma
Toxicity
- Metranidazole
- Lead
Vascular
- Arteriovenous malformation
- Infarction
- Feline ischaemic encephalopathy
- Haemorrhage
- Hypertension
Diagnosis
- Diagnosis must encompass the following:
History
- Aside from the normal history, there are several very important questions to be asked:
- Has there been any possible exposure to toxins or trauma?
- What is the animal's diet?
- Are the litter mates normal?
- Are there any specific clinical signs that may relate to a particular diagnosis?
- E.g. hypersalivation - commonly seens in young animals with portosystemic liver shunts.
Physical Examinations
- Check for signs of systemic disease.
- Ocular changes with FIP, toxoplasmosis, FeLV or lysosomal storage diseases.
- Ascites with with FIP, liver or cardiac disease.
Neurological Examination
- This should include CN examination, postural reactions, spinal reflexes and sensory examination.
Blood and Urine Tests
- Blood tests should include haematology and serum biochemistry.
- These are particularly helpful in the diagnosis of many systemic and especially metabloic conditions.
Infectious Disease Tests
- E.g. FeLV and FIV, toxoplasma IgM and IgG tests.
CSF Analysis
- Particularly useful in the diagnosis of:
- Inflammatory diseases
- E.g. FIP
- Lymphoma
- Inflammatory diseases
Imaging
- Radiographs of the chest and abdomen
- Abdominal ultrasonography
- MRI or CT scans
- Examine the structure of the brain and determine presence or absence of inflammation or neoplasia.