Lecture 8 Lymphedema: Pathophysiology & Diagnosis Flashcards

1
Q

Primary vs. Secondary Lymphedema

A
  • Primary: Absence/decrease of lymphatic vessels
  • Secondary: acquired through cancer, trauma, and infection
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2
Q

Primary Lymphedema: Aplasia

A
  • missing function of lymphatic system
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3
Q

Primary Lymphedema: hypoplasia

A
  • not enough lymphatic system
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4
Q

Function of the lymphatic system

A
  1. absorption and transport of lymph assists venous circulation
  2. Immunological
  3. Digestion
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5
Q

what is the percentage of interstitial fluid that lymph system & venous system collects?

A
  • Lymph system collects 10-20%
  • Venous system collects 80-90%
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6
Q

How are the Lymphatics run to the circulatory system?

A
  • Parallel
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7
Q

Fluid pathway of Lymphatic System

A
  • unidirectional flow only toward heart
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8
Q

Superficial and deep pathways of Lymphatic system

A

Interstitial spaces > Lymphatic capillaries > Pre-collectors > Collectors > Lymph nodes > Trunks > Ducts > Venous angles (subclavian veins) > Venous circulation

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9
Q

Where are lymph vessels not fond

A
  • Brain and Spinal Cord
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10
Q

Lymphatic Capillaries

A
  • no valves, lymph can flow in any direction
  • allow us to manipulate the drainage pathway
  • Main function = Absorption
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11
Q

Collectors

A
  • Have valves: unidirectional
  • “micro hearts”
  • Function = Transport
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12
Q

Function of Lymph nodes

A
  • Produce lymphocytes
  • Trap foreign matter
  • Regulates fluid volume
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13
Q

Function of the ducts

A
  • Empty lymph fluid into the blood circulation at the right and left venous angles
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14
Q

Thoracic Duct

A
  • drains 75% of the body’s lymph fluids
  • Starts around L2 level
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15
Q

Right Lymphatic Duct

A
  • drains 25% of the body’s lymph fluid
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16
Q

Major watershed area

A
  • Mid sagittal
  • transverse
  • calvicular
  • spine of scapula
  • gluteal
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17
Q

Function of Anastamoses

A
  • allow for fluid exchange
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18
Q

What are the regional lymph node groups

A

Axillo-axillary
Interinguinal
Axillo-Inguinal

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19
Q

Fluid Transport out of capillaries

A
  • Arterial Side
    -Blood Capillary pressure (BCP)
  • Colloid osmotic pressure interstitiel (COPi)
20
Q

Fluid transport into capillaries

A
  • Venous side
  • Interstitial Pressure
  • Colloid Osmotic Pressure Plasma (COPp)
21
Q

Starling’s Law: fluid balance is even

A

BCP = COPp

22
Q

Starling’s Law: Arterial

A

BCP > COPp = Ultrafiltration

23
Q

Starling’s law: Venous

A

BCP < COPp = Reabsorption

24
Q

Lymphatic Transport

A
  • No central pump or heart equivalent
25
Q

Lymphatic fluid is transported via

A
  • intrinsic contractions
  • Lymph volume
  • Skeleteal muscle contraction * Ankle Pump
  • Arterial pulsation
  • Respiratory pressure changes
  • External pressure
26
Q

Lymphedema defined

A
  • Abnormal accumulation of protein rich fluid causing chronic inflammation and reactive fibrosis
27
Q

Pathophysiology of Lymphedema

A

Reduced lymph transport capacity > Mechanical insufficiency & less protein absorbed > Increased protein draws more fluid out of capillaries > increasing ultrafiltration > edema

28
Q

Lymphedema leads to

A

Increase in infection risk

29
Q

Primary Lymphedema is caused by?

A
  • Lymphatic dysplasia
  • More often in females and in the Lower extremities
30
Q

Milroy’s disease is a form of?

A
  • Primary lymphedema
31
Q

Secondary Lymphedema can be caused by?

A
  • filariasis, cancer, trauma, infection, surgery, radiation, CVI
32
Q

Highest risk to develop Breast cancer-related lymphedema?

A
  • ALND + radiation therapy (Axillary lymph node dissection)
33
Q

What is something to be aware of BCRL?

A
  • Typically occurs within 1 year of cancer treatment but can develop years after
34
Q

What does Limb Alert mean?

A
  • no blood pressure & No IVs
35
Q

Clinical Characteristics of both types

A
  • starts distally
  • pitting in early stages
  • fibrosis in mid stages
  • skin changes in later stages
  • positive stemmer signs
  • rarely painful
36
Q

How does Lymphedema progress through the stages

A
  • progressive, but no consistent pattern
37
Q

Stage 0

A
  • transport capacity reduced
  • no real objective differences
  • no edema detectable
38
Q

Stage 1

A
  • Accumulation of protein rich fluid
  • Pitting may be present
  • reduces with elevation
  • no fibrosis
39
Q

Stage II

A
  • Constant girth increase
  • Pitting & fibrosis present
  • elevation doesn’t reduce swelling
40
Q

Stage III

A
  • Non Pitting edema (fibrosis)
  • skin changes: thickening, hyperpigmentation, increased skin folds, fat deposits
41
Q

Positive Stemmer’s sign

A
  • dorsal skin of the second toe/finger can’t be easily lifted away from the bone
42
Q

3 main tissue texture

A
  • soft
  • spongy
  • firm
43
Q

Girth Measurements

A

Mild: < 3 cm difference between affected and unaffected limbs
Moderate: 3-5cm difference between affected and unaffected limbs
Severe: > 5cm difference