lymphedema Flashcards
lymphatic system
- 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
lymph
- originates as component of interstitial fluid
- consists of water, proteins, fatty acids, cellular components
flow of lymph
- 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
lymphatics collect _ % of interstitial fluid, while venous system collects other - %
lymphatics 10-20%
venous system 80-90%
lymphatic system under control of
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
lymph nodes
- 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
lymphedema
- 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
primary lymphedema
- 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
secondary lymphedema
- 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
3 types of insufficiencies in LS that lead to lymphedema
- 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
diagnosis of lymphedema
- 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
most common method for measuring lymphedema
circumferential measurements
circumferences for limb edema
- 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
classification measurements for lymphedema
- 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
other options to measure lymphedema
volumetric measurements
goniometry
MMT
pain assessment
sensory testing
skin inspection
bioelectrical impedance
gait and balance
lymphedema staging
- 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
lymphedema treatment - complete decongestive therapy
CDT
- 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
other lymphedema treatments
- 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
contraindications of decongestive therapy
- acute infection
- cardiac edema
- DM
- HTN
- malignancy
- renal insufficiency
- DVT
filariasis
- parasitic infection most often seen in tropical climates
- one of the most common causes of secondary lymphedema worldwide
hyperkeratosis
thickening of outermost layer of skin, typical with stage 3 lymphedema
lymphadenitis
- infeciton and inflammation of a lymph node
- acute or chronic
milroy’s disease
- inherited type of primary lymphedema in infancy
- BLE edema most common s/s
non-pitting edema
- harder fluid accumulation, not compressible when pressure applied
- in later stages of lymphedema
papilloma
- benign wart-like skin growth typically observed w/ stage 3
pitting edema
- fluid accumulation that can be compressed and indents with pressure
- early stages
spleen
- organ in LUQ
- filters RBCs and produces antibodies to fight infection
stemmer’s sign
- 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
thymus
- organ posterior to sternum and anterior to heart
- produces T cells and T lymphocytes to help combat infection