lymphedema Flashcards

1
Q

lymphatic system

A
  • collection and transportion of fluids and other materials that are not reabsorbed by venous system, maintenance of fluid balance within body, immunse defense
  • network of superficial and deep lymph vessels that transport lymph throughout body
  • lymph vessels located anywhere blood supply exists - except brain and SC
  • other components - thymus, bone marrow, spleen, tonsils, peyer patches in small intestine: production of lymphocytes for immune system
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1
Q

lymph

A
  • originates as component of interstitial fluid
  • consists of water, proteins, fatty acids, cellular components
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2
Q

flow of lymph

A
  • initial vessels near blood capillaries - collect fluid from interstitium not picked up by venous systems
  • intial vessels -> lymph collectors -> lymphatic trunks (R lymphatic duct - R arm and R side of head; thoracic duct - rest of body) -> venous system via subclavian veins

lymphatics transport most extracellular proteins - too large

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3
Q

lymphatics collect _ % of interstitial fluid, while venous system collects other - %

A

lymphatics 10-20%
venous system 80-90%

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4
Q

lymphatic system under control of

A

ANS - produces contractions of smooth muscles within lymph vessels to move lymph
- also moved by skeletal muscle contraction compressing lymph vessels
- one-way valves maintain unidirectional flow of lymph

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5
Q

lymph nodes

A
  • neck, axilla, chest, abdomen, groin
  • collect lymph from adjacent areas
  • function to filter wate products and foreign materals (bacteria, viruses) - provide immune system defense with use of T and B lymphocytes
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6
Q

lymphedema

A
  • chronic, incurable
  • accumulation of protein-rich fluid (lymph) in body -> edema
  • usually in extremities, face, neck, abdomen, genitalia, trunk
  • fluid accumulation s/t daage to lymph structures
  • primary or secondary
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7
Q

primary lymphedema

A
  • d/t abnormal development of lymphatic system from birth
  • can take years to be symptomatic
  • abnormalities can include absence of lymph vessels, decreased number/size of lymph vessels, increased size of lymph vessels -> incompetent valves
  • more often in female, more often in LEs
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8
Q

secondary lymphedema

A
  • d/t some other disease or injury damaging LS
  • trauma, surgery, radiation, tumor growth, multiparity, chornic venous insufficiency, infection
  • in US, breast cancer surgery and treatment is most common cause
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9
Q

3 types of insufficiencies in LS that lead to lymphedema

A
  • dynamic: excess lymph circulating in LS that exceeds transport capacity of system; results in pitting edema -> chronic venous insufficiency, CHF, pregnancy
  • mechanical: transport capacity of system reduced d/t to damage to LS; results in protein-rich, non-pitting lymphedema
  • combined: both an increase in lymph and decrease in transport capacity
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10
Q

diagnosis of lymphedema

A
  • medical history, exam, imaging
  • direct lymphography: injection of contrast medium into lymph vessel for visualization of entire lymph system through radiography; not common
  • indirect lymphography: injection of water-soluble medium under skin to allow for visualization of smaller superficial lymph vessels
  • lymphoscintigraphy: injection of radioactive material for visualization through nuclear medical imagaing, preferred over direct d/t fewer complications
  • MRI and CT: ID tumors that may cause lymphedema
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11
Q

most common method for measuring lymphedema

A

circumferential measurements

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12
Q

circumferences for limb edema

A
  • 7 circumferences recommended for UE and LE to deduce fluid has been removed and not just redistributed
  • use opposite limb for comparison if able - differences of 2-3 cm between 4 circumferences on BUEs is lymphedema
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13
Q

classification measurements for lymphedema

A
  • mild: < 3 cm difference btw affected and unaffected limbs
  • moderate: 3-5 cm difference btw affected and unaffected limbs
  • severe: > 5 cm difference between affected and unaffected limbs
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14
Q

other options to measure lymphedema

A

volumetric measurements
goniometry
MMT
pain assessment
sensory testing
skin inspection
bioelectrical impedance
gait and balance

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15
Q

lymphedema staging

A
  • 0: latent (preclinical) stage, no visible edema though capacity oflymph system has been affected
  • 1: reversible stage, pitting present and increases with activity or heat but diminishes with elevation and rest
  • 2: spontaneously irreversible stage; non-pitting, does not change wiht elevation or rest; fibrotic skin changes, risk of infection increases; Stemmer’s sign (+, cannot pinch skin)
  • 3: lymphostatic elphantiasis stage, non-pitting, significant fibrotic changes, presence of papillomas, deep skinfolds, hyperkeratosis, infection, (+) stemmer’s
16
Q

lymphedema treatment - complete decongestive therapy

CDT

A
  • manual lymphatic drainage (MLD): techniques to move lymph around blockages to draining areas, uninvolved areas first to prep then involved
  • compression thearpy: maintains reduction in edema from MLD, short stretch bandages used - low resting pressure (do not constict lymph flow like long-stretch bandages), use different fitted garments at night, use graded compression for more pressure distally
  • exercise: increase lymph vessel contraction, muscle pump to stimulate flow; trunk then extremity exercise w/ proximal to distal, deep breathing; should use compression bandages and garments when exercising
  • skin care: more prone to damaged skin bc protein-rich fluid impairs immune system function - allows for bacterial and fungal growth; should prevent issues - inspect skin, moisturize
17
Q

other lymphedema treatments

A
  • no meds or surgical procedures
  • debulking - sx to remove excessive skin that forms in later stages of disease; can damage existing lymph vessels and further accelerate disease course
  • intermittent pneumatic compression devices - some concern if pressure is too high might damage lymphatic vessle s
18
Q

contraindications of decongestive therapy

A
  • acute infection
  • cardiac edema
  • DM
  • HTN
  • malignancy
  • renal insufficiency
  • DVT
19
Q

filariasis

A
  • parasitic infection most often seen in tropical climates
  • one of the most common causes of secondary lymphedema worldwide
20
Q

hyperkeratosis

A

thickening of outermost layer of skin, typical with stage 3 lymphedema

21
Q

lymphadenitis

A
  • infeciton and inflammation of a lymph node
  • acute or chronic
22
Q

milroy’s disease

A
  • inherited type of primary lymphedema in infancy
  • BLE edema most common s/s
23
Q

non-pitting edema

A
  • harder fluid accumulation, not compressible when pressure applied
  • in later stages of lymphedema
24
Q

papilloma

A
  • benign wart-like skin growth typically observed w/ stage 3
25
Q

pitting edema

A
  • fluid accumulation that can be compressed and indents with pressure
  • early stages
26
Q

spleen

A
  • organ in LUQ
  • filters RBCs and produces antibodies to fight infection
27
Q

stemmer’s sign

A
  • diagnosis of lymphedema
  • (+) if skin at dorsal base of second toe/finger can’t be easily lifted away from bone - indicates thickening of skin d/t fibrotic changes
28
Q

thymus

A
  • organ posterior to sternum and anterior to heart
  • produces T cells and T lymphocytes to help combat infection