Other Systems - Pathology Flashcards

1
Q

What does lymph fluid consist of?

A

Water, protein, fatty acids, and cellular components. Originates as a component of the interstitial fluid

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2
Q

where are vessels located

A

Everywhere except for the brain and spinal cord

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3
Q

What is the function of the initial lymph vessels

A

Collect fluid from the interstitium that is not picked up by the venous system.
Smallest vessel.
Located near blood capillaries.

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4
Q

The lymphatic system do?

A

Transports majority of extra cellular proteins since they are too big to be carried in the Venous system.

  • Nodes are contained throughout the lymphatic system in the neck, axilla, chest, abdomen, and groin.
  • Lymph nodes collect lymph and filter waste products such as bacteria and viruses. contribute to Immune system defense with B and T cells
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5
Q

How much interstitial fluid is collected by the lymphatic system? The venous system?

A

lymphatic system: 10-20%

venous system 80-90%

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6
Q

The path that lymph follows in the lymphatic system

A

Initial lymph vessels > Lymph collectors > lymph trunks

each vessel type is larger than the last.
Trunks: R lymphatic trunk will collect from R arm and R side of head
Thoracic duct collects lymph from everywhere else
- vessels will empty into subclavian vein into the venous system

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7
Q

Two main lymphatic trunks and what do they drain

A
  • Right lymphatic duct :drains right arm and right side of the head.
  • Thoracic duct drains the remainder of the body.
  • Vessels empty lymph directly into the Venice system via subclavian vein
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8
Q

What are other components of the lymphatic system

A

Thymus, bone marrow, spleen, tonsils, Peyer patches in small intestine. Help create lymphocytes which are important for the immune system

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9
Q

What is lymphedema

A

Accumulation of protein rich fluid that is incurable. Results in edema in the body that accumulates in the face, neck, abdomen,genitalia and trunk

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10
Q

Primary lymphedema

A

-Occurs due to abnormal development that may happen at birth.
- May take several years for symptoms to arise.
-Absence of lymph vessels, decrease in number or size of lymph vessels and/or increased size makes valves in competent.
_ usually seen in females and in lower extremities

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11
Q

secondary lymphedema

A

Occurs secondary to disease or injury that damages lymphatic system.
Breast cancer surgery treatment is the most common cause for secondary lymphedema.

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12
Q

What are three types of insufficiencies that can lead to lymphedema

A

Dynamic insufficiency
Mechanical insufficiency
combined insufficiency

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13
Q

Dynamic insufficiency

A

Dynamic insufficiency - most common type of insufficiency.
Excess lymph circulates and exceeds transport capacity.
-Results in pitting edema.
-Chronic heart failure Venice insufficiency and pregnancy

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14
Q

Mechanical insufficiency

A

Mechanical insufficiency - Transport capacity of system is reduced due to damage of lymph system.
Results in more protein rich lymphedema/ non-pitting edema

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15
Q

combined insufficiency

A

combined insufficiency

Increase of lymph fluid and decrease of transport capacity

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16
Q

What happen if lymphedema progresses

A
  • Valves expand and become incompetent and leads to further fluid accumulation.
  • When fluid stasis continues proteins degrade and lead to chronic inflammation and eventual fibrotic changes of nearby tissues.
  • Fibrosis leads to hypoxia and causes further chronic inflammation and risk for infection
17
Q

What are ways to prevent lymphedema

A

Avoid skin injury with razors nail clippers, skin moisturizers, puncture such as blood draws on affected limb

  • Avoid Constriction by avoiding loose fitting clothing and blood pressure measurements on limb
  • Monitor limb while exercising take frequent rest breaks during intense activity
  • Avoid hot and cold temperatures leads to fluctuations in lymphedema.
  • Wear compression garments during strenuous activity or prolonged periods of time when traveling on airplanes.
  • Maintain healthy weight avoid being overweight, diet and exercise
18
Q

phenylketonuria

A

Intellectual disability, behavioral and cognitive issues due to elevated serum phenlalanine (normally converted to tyrosine)

  • Autosomal recessive.
  • Most common and Caucasian.
  • If left untreated severe intellectual disability will occur adequate prevention will avoid all manifestations of disease.
  • After accumulation: gait disturbances, hyperactivity, psychosis, abnormal body odor and lighter skin occur
19
Q

Tay-sacs disease (lysosomal storage disorder)

A
  • Absence/deficiency of hexoaminedase Result in an accumulation of gangliosides in the brain.
  • Autosomal recessive
  • Carried primarily by Jewish people
  • At six months children miss developmental milestones, deteriorate motor and cognitive skills.
  • With disease progression significant intellectual disability and paralysis
  • death by age of five.
20
Q

Wilson’s disease (hepatolenticular degeneration)

A

Deficit in the body’s ability to metabolize copper. Copper accumulates overtime in brain liver cornea kidney and tissues

21
Q

What control movement of lymph

A
  • under control by the ANS system to coordinate smoth muscle contraction in vessel walls
  • muscle contraction also moves and compresses vessles for fluid movement