Umn LMN Adn2015

Download as pdf or txt
Download as pdf or txt
You are on page 1of 65
At a glance
Powered by AI
The key takeaways are that UMN and LMN diseases present with distinct symptoms, gait evaluation is important for localization, and diseases can look similar without thorough examination.

UMN dysfunction causes spasticity, hyperreflexia and abnormal postures while LMN dysfunction causes hypotonia, hyporeflexia and rapid muscle atrophy.

Symptoms of UMN dysfunction will be present in limbs downstream from a CNS lesion while LMN symptoms are only present if the motor nerve or intumescence is affected. Localization depends on whether symptoms are isolated to one limb or generalized.

Upper Motor Neuron

Lower Motor Neuron

David Brewer DVM, DACVIM (Neurology)


Objectives
• Fundamental differences between the UMN
and LMN systems
• Typical symptoms seen with dysfunction
• Role in neurolocalization

• Cases examples
UMN? LMN? Who Cares?
• Localization

4
Definitions
• UMN- The neurons of the brain that
control motor activity of the body

5
Definitions

• UMN- Cell bodies are


located in the cerebrum
and brainstem
• Entire UMN is confined
to CNS

6
Definitions
• LMN- the neurons that directly innervate
the muscles.

7
Definitions
• LMN- Cell bodies are located in the ventral
gray horn of the spinal cord

8
Functions
• UMN
• ‘Tells’ the LMN what to do
• Stimulate or inhibit the
LMN
• Initiation of voluntary
movement
• Maintenance of muscle
tone and support against
gravity
• Regulation of posture

9
Functions
• LMN-
• Receives inputs from
the UMN
• Connects the CNS
with the muscles
• Spinal reflexes

10
Dysfunction of the UMN
• Paretic (weakness) to paralysis
• Gait: (if still walking)
• Long strided
UMN
• Crossing Ataxia
• Scuffing
• Loss of inhibition:
• Spasticity
• Hyperreflexia / hypertonia /
abnormal reflexes
• Abnormal postures (brain lesion)
• Ex. opisthotonus

11
Dysfunction of the UMN
• Gait Generation
▪ Dogs/cats- brainstem
▪ People- cerebrum
Romy
Romy
Romy
Romy
Tonic Gamma Loop Mechanism2
Loss of Inhibition

1.Gravity (pleximeter)
stimulates muscle spindle

2. Firing along Ia afferent


1 3. Stimulation of alpha motor
neuron and muscle
3 contraction

** Must be controlled by
UMN system
Crossed Extensor Reflex
Dysfunction of the LMN
• Paretic (weakness) to paralysis
• Gait: (if still walking)
• Short-strided
• Choppy
• Lame
• Hypotonia
• Hyporeflexive
• Rapid muscle
atrophy

20
Postural Reactions
• Both UMN and LMN
lesions can cause
abnormal postural
reactions
• More so with UMN
• Depends on severity
Goal: Neurolocalization
• How do we use UMN and LMN
symptoms to help localize a lesion?

22
Goal: Neurolocalization
• The location of the lesion along the neuroaxis
will determine which limbs are affected
▪ UMN symptoms will be present in limbs
downstream from a CNS lesion
▪ LMN symptoms will only be present if the
motor nerve or the intumescence is
affected
24
Goal: Neurolocalization
• Symptoms can be isolated to one limb or
generalized to all limbs.
• Not every symptom needs to be present to
localize a region
Diffuse
Brain C1-C5 C6-T2 T3-L3 L4-S3
LMN

TL UMN UMN LMN Normal Normal LMN

PL UMN UMN UMN UMN LMN LMN

26
UMN or LMN Bladder?

27
Diffuse
Brain C1-C5 C6-T2 T3-L3 L4-S3
LMN

TL UMN UMN LMN Normal Normal LMN

PL /
UMN UMN UMN UMN LMN LMN
Bladder

28
Bladder
• UMN Bladder
▪ Seen with lesions cranial
to L4
▪ Loss of inhibition causes
excess tone on the
urethral sphincters
▪ Large difficult to express
▪ Overflow incontinence
UMN Bladder Treatment
• Relax Internal Urethral Sphincter
▪ Alpha-adrengeric antagonist
▪ Ex. Phenoxybenzamine or Prazosin

• Relax External Urethral Sphincter


▪ Skeletal muscle relaxant
▪ Ex. Diazepam
Bladder
• LMN Bladder
▪ Seen with lesions caudal
to L4
▪ Hypotonia of the
urethral sphincters
▪ Fills partially
▪ Continuous dribbling
▪ Easy to express
LMN Bladder Treatment
• Promote Bladder Contraction
▪ Stimulate muscarinic receptors
• Ex. Bethanechol
Technically Speaking
• LMN is referencing
just the nerve

• What about the


muscle or the
junction between the
nerve and muscle?
Neuromuscular System
• LMN (Neuropathy)
• Muscle (Myopathy)
• NMJ (Junctionopathy)
Neuromuscular System
Myopathy Neuropathy NMJ

Muscle mass/tone Normal to ↓ ↓ Normal

Gait Paresis Paresis Paresis may be episodic

Postural Reactions Normal


↓ Normal

Reflexes Normal
↓ Normal
Case Example 1
• Middle-age German Shepherd
• CC: Wobbly in the pelvic limbs
37
Diffuse
Brain C1-C5 C6-T2 T3-L3 L4-S3
LMN

TL UMN UMN LMN Normal Normal LMN

PL /
UMN UMN UMN UMN LMN LMN
Bladder

38
Differentials
• C6-T2 myelopathy
▪ Degenerative - IVDD
▪ Anomalous – Wobbler’s syndrome
▪ Metabolic - ??
▪ Neoplastic- Extradural or intramedullary
▪ Inflammatory- Immune-mediated or infectious
▪ Traumatic / Toxic- Contusion
▪ Vascular- FCE
Diagnostics
Diagnosis
• C6-T2 myelopathy

▪ Anomalous – Wobbler’s syndrome


Treatment and Outcome
• Treatment
▪ Owner elected conservative management

• Outcome
▪ Fair to good response to prednisone and life
long gabapentin
Case Example 2
• Young Bichon
• CC: Down in pelvic limbs
44
Diffuse
Brain C1-C5 C6-T2 T3-L3 L4-S3
LMN

TL UMN UMN LMN Normal Normal LMN

PL /
UMN UMN UMN UMN LMN LMN
Bladder

45
Differentials
• T3-L3 myelopathy
▪ Degenerative - IVDD
▪ Anomalous – Malformation, cyst
▪ Metabolic - ??
▪ Neoplastic- Extradural or intramedullary
▪ Inflammatory- Immune-mediated or infectious
▪ Traumatic- Contusion
▪ Vascular- FCE
Diagnostics
Diagnosis
• T3-L3 myelopathy
▪ Degenerative - IVDD
Treatment and Outcome
• Treatment
▪ Hemilaminectomy

• Outcome
▪ Normal at 6 weeks post surgery
Case Example 3
• Young adult Giant Schnauzer
• CC: Down in all 4
53
Diffuse
Brain C1-C5 C6-T2 T3-L3 L4-S3
LMN

TL UMN UMN LMN Normal Normal LMN

PL /
UMN UMN UMN UMN LMN LMN
Bladder

54
Differentials
• Diffuse LMN Disease
▪ Degenerative – Hereditary?, Storage diseases
▪ Anomalous – ?
▪ Metabolic – Endocrine (DM, cortisol, thyroid)
▪ Neoplastic- Lymphoma, paraneoplastic
▪ Inflammatory- Polyradiculoneuritis, infectious – protozoal,
(botulism)
▪ Traumatic / Toxic- (Tick paralysis)
▪ Vascular- ?
Diagnostics
Diagnostics
• CBC – Normal
• Chem – Normal
• Urinalysis – Normal
• 3 view chest radiographs – Normal
• Abdominal Ultrasound – Normal
• Baseline cortisol and T4 – Normal
Additional Diagnostics
• Electrodiagnostics
▪ Electromyography
▪ Motor Nerve Conduction Velocity
▪ F-Waves
• +/- Muscle nerve biopsy
Updated Differentials
• Diffuse LMN Disease
▪ Degenerative – Hereditary?, Storage diseases

▪ Neoplastic- Lymphoma, paraneoplastic


▪ Inflammatory- Polyradiculoneuritis, infectious – protozoal,
(botulism)
▪ Traumatic / Toxic- (Tick paralysis)
Treatment and Outcome
• Treatment
▪ Frontline application

• Outcome
▪ ~2 weeks later – 90%
▪ ~4 weeks later – 100%
Presumptive Diagnosis
• Diffuse LMN Disease

▪ Inflammatory- Polyradiculoneuritis,
Case Example 4
• 2 yr old Newfoundland
• CC: Unable to walk
Case Example 4
Take Home Points
• UMN disease should have distinctly different signs
from LMN disease

• Cervical spinal cord disease and diffuse LMN disease can sometimes be
confused without thorough examination

• Diseases that affect the neuromuscular system can look very similar

• Gait evaluation is probably the most important aspect of the exam

• Acute localization is key!


QUESTIONS?

You might also like

pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy