Subcutaneous tissue Flashcards

(49 cards)

1
Q

Osmolality

A

is of prime importance in maintaining homeostatic balance b/w ICF + ECF
- IS THE MEASULE OF SOLUTE CONCENTRATION AND IS DEFINED AS THE NUMBER OF THE OSMOLES OF SOLUTE PER KILOGRAM OF WATER ( osm/L)

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2
Q

Osmolarity

A
  • is the measure of osmoles of solute per liter of solution (osm/L)
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3
Q

Electrolytes

A

ionized substances which contribute most to the total solute concentration / ( osmolality ) of body fluids

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4
Q

From Vascular space -> Extracellular space

A
  1. Hydrostatic pressure from vascular system

2. Coloid oncotic pressure of interstitium

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5
Q

To vascular compartment

A
  1. Coloid - oncotic pressure ( plasma protein )

2. Hydrostatic pressure - Interstitial

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6
Q

Edema

A

Palpable swelling produced by expansion of the interstitial fluid volume

  • accumulation of fluid in intercellular spaces ( Interstitium )
  • clinical evident only after accumulation of a few liters
  • preceded by increased G with 4-5 kg ( PreEdema not evident at clinical exam -> loop diuretic decreases G )
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7
Q

From capillary arteriolar end to the interstitium

A

Return from interstitialto vascular space through :

  • venous capillary end
  • lymphatics
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8
Q

Edema

Mechanisms

A
  1. ↑ venous pressure
  2. ↓ plasma oncotic pressure
  3. ↑ capillary permeability
  4. obstruction venous and lymphatic vessel
  5. hydro-saline retention at kidney level
    Increased water and salt capital of the body
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9
Q

MECHANISMS: Imbalance between forces

EDEMA

A
  1. Obstruction of venous system → ↑ Capillary press. → edema
  2. 🡫 coloid oncotic pressure - in hypoalbuminemia
  3. capillary endothelium dysfunction- ↑ capillary permeability
    - injury by chemical agents , bacterial, thermal, mechanical
    - protein transfer to interstitium
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10
Q

Edema Lymphatic drainage

A
  1. Safety supplementary mechanism
  2. It takes on the albumin filtered through the capillary wall and the excess of the transudated fluid
  3. Reduces lymphatic flow
  4. Essential role in the production of lymphedema
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11
Q

EDEMA

CLINICAL ASPECT

A
  1. Swelling- Increased volume of a region
  2. Disappearance of anatomical reliefs
  3. Pitting edema (usually pressed on a bony plane)

occur in areas with lax connective tissue where
interstitial pressure is small (retromaleolar, face,
eyelid)

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12
Q

EDEMA: General Characteristics

A
  1. Initial stage (Preliminary stage)
    - Shiny & tight edematous skin
  2. The resorption stage
    - Fine longitudinal folds (“wrinkly” skin)
    - Stretch marks (thigh and abdomen)

Chronic Stage
- Thickening / rigidity of the tegument (hyperplasia of
subcutaneous cellular tissue ←↑ interstitial press over longtime)
- Lichenoid appearance (fibroblastic proliferation)
- Harsh to the touch
- Marked peeling
- Pit difficult to evoke→ pitting only after prolonged compression
- Dystrophic skin (cracks, wet ulcerations)

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13
Q

EDEMA: General Characteristics

A

COLOUR
Red: inflammatory and allergic edema
White: renal edema
Cyanotic (ocher dermatitis):cardiac & venous edema

LOCAL TEMPERATURE

Increased: inflammatory edema

Normal: renal edema

Reduced: cardiac edema

CONSISTENCY

Elastic, let the pit easily → renal & carential edema

Hard ~ non pitting→ inflammatory & venous edema

PAIN
Painless = most edema of general cause
Painful = inflammatory edema

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14
Q

Renal edema

A

🡫 coloid osmotic pressure

↑ capillary permeability

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15
Q

Hepatic edema

A

🡫 coloid osmotic pressure - due to hypoalbuginemia

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16
Q

CARDIAC EDEMA

A

↑ venous pressure (venous congestion)

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17
Q

CARENTIAL EDEMA

A

↓ oncotic pressurei by hypoproteinemia

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18
Q

ANASARCA

A
Generalized edema
- Fluid effusion in body cavities associated
Biology: TRANSUDATE
- Serocitrine
- Low proteine level
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19
Q

ANASARCA- characteristics

A
  1. Generalized (not from the beginning)
  2. Start at lower limb (retromaleolar, anterior tibial)
  3. Infero intern area of thigh, just above the knee
  4. Abdominal wall (orange peel appaerance)
  5. Lumbosacral area
  6. Anterior thorax
  7. Posterior thoracx
  8. Uppr limbs (infero-intern & posterior, above the
    elbow)
  9. Face (eyelid edema)
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20
Q

PREGNANCY EDEMA

A
Moderate edema
- White
- Soft
- Pitting Easy
- Lower limb usually
- In late pregnancy
- Pregnancy nephropaty – Eclampsia - Particular aspect : 
> Week 20
> Generalized Edema
> HTN
> Proteinuria
21
Q

CATAMENIAL EDEMA

A

Moderate Edema at lower limbs
In women in the second half of the menstrual cycle
Trigger hormonal

22
Q

MIXEDEMA

A

In severe hypothyroidism
Pitting
+ thickened skin

23
Q

IATROGENE

A

DRUG INDUCED

  • corticosteroids
  • estrogens
  • BP lowering drugs (dihidropiridine, α blockers)
24
Q

IDIOPATIC EDEMA –

Milroy Syndrome

A

Ussualy at the calves level
Womens > 30 y old
Chronic Edema with unknown etiology

25
INFLAMATORY EDEMA
1. Localized edema (tumor) 2. Unilateral usualy 3. Warm (calor) 4. Painful (dolor) 5. Redness of the skin (rubor) 6. One of the signs of inflammation Characterize: erysipelas, lymphangitis, arthritis, abscess, cellulite, osteomyelitis, phlebitis,..
26
ALERGIC EDEMA | Characteristics
Colour: red Temperature: warm Painfull Non-pitting !!!! Sudden onset Characteristic location: - Face, eyelid, lips, tongue Asociated symptoms - Pruritus - Urticaria
27
ALERGIC EDEMA | Forms:
``` Acute, Chronic, Recurrent Quincke Angioneurotic Edema - Sudden onset - Disapearance: hours, days - Without pruritus !!!!!! Associated with: - glotic edema - asphyxia - paroxysmal inspiratory dyspnoea caused by different allergens (food, medicines) ```
28
LYMPHEDEMA
- Pale - Start asymetricaly - Soft initially, then it becomes card boarded with lichenifications - Unusual locations: dorsal area of the hand, feet Mechanism: - Blockage of lymphatic circulation through - Malformations of the lymphatic vessels - Tumors - Metastases - Postoperative: resection of the lymphatics - After irradiation of the lymph nodes - In filariasis - grotesque aspect "elefantiazis arabicum" - Forms: congenital, acquired
29
VENOUS EDEMA
Superficial thromboflebitis - Edema around the superficial afected vein - Present with inflammations signs Deep vein thrombosis - Edema characteristics: white, painful spontaneously and with palpation, (positive Homans sign) - Swelling of the affected area (ex. calve, thigh) - Superficial vein network prominent - Superimposed arterial spasm may determine cyanosis
30
VENOUS EDEMA
Chronic venous insuficiency - Secondary to varicose veins or repeated deep vein thrombosis - Unilateral or bilateral but uneven - Especially on the lower limbs - Accentuated in orthostatism - Cyanotic skin, with ocher dermis - Possibly complicated by ulcers
31
EDEMA in superior cava vein syndrome
swelling in the face, neck, arms, and upper chest | sometimes with a bluish-red skin color
32
EDEMA in superior cava vein syndrome | Mechanism
- Obstruction of superior cava vein - ↑ venous pressure above the SCV obstruction - Colateral circulation associated
33
DEPENDENT (GRAVITATIONAL) EDEMA
- Determined by prolonged gravitation effect - Long duration trip - In patient with critical limb arterial ischemia due to prolonged sitting as attempt to diminish the related pain - Favored by hot season
34
NEUROTHROPHIC EDEMA
- Moderate edema - It affects the paralyzed limb - The typical appearance = "juicy hand" described by Marinescu
35
DEHYDRATION
Clinical condition caused by a reduction in content water of the body CLASSIFICATION - Cellular dehydration - Extracellular dehydration
36
Cellular dehydration (1)
- Determined by ↓ volume of intracellular water, due to the loss of water through: polyuria, perspiration, respiration (in coma) - It may accompany edema (extracellular hyperhydration) when the patient ↓ fluid intake, maintaining salt intake - May accompany extracellular dehydration resulting in global dehydration
37
Cellular dehydration (2)
Clinical aspect - Thirsts (by stimulating the hypothalamic osmometer) - Nausea-free anorexia - Dry tongue and mouth due to decreased parathyroid secretion - Fever (by altering the thermoregulation) - Neurologic phenomena (cheyne-stokes breathing, delirium, drowsiness, coma) Biology: Natremia > 145 mEq/l ↑ plasma osmotic Pressure Oliguria + ↑ urinary density
38
Extracellular dehydration (1)
It is the consequence of the predominant losses of sodium by the way: - kidney (nephropathies, excess diuretics) - digestive (vomiting, diarrhea) - skin (profuse sweating) - drastically reducing the salt intake
39
Extracellular dehydration (2)
Clinical aspect: - The patients are not thirsty - Persistent skin fold through the 🡫skin turgor - Eyeball hypotony - Colaps, hypotension, by reducing circulating volume - Tachycardia oliguria (with high urinary density) Biology: - Natremia usually normal - Hemoconcentration !!!!!!!!! - Hyperazotemia !!!!!! It can be associated with cellular hyperhydration by migrating water inside the cells, a state characterized by apathy, headache , vomiting ( cerebral edema )
40
Launois-Bensaude Syndrome: A Benign Symmetric | Lipomatosis -Madelung disease
Multiple symmetrical lipomatosis, Launois-Bensaude syndrome, cephalothoracic lipodystrophy, Madelung disease, Brodie's syndrome, Buschke's disease, “Fat neck”
41
Launois-Bensaude Syndrome: A Benign Symmetric Lipomatosis -Madelung disease Characteristics
occurs mostly in men between 30 - 60 y with known alcohol use - more common in Mediterranean countries -characterized by the presence of fat masses: - large size - located symmetrically in various parts of the body (but mainly in the cervical region) - slightly circumscribed (diffuse outline, no limiting capsule) - soft consistency - painless - it develops progressively in the subcutaneous tissue - in evolution, it often infiltrates neighboring structures histological: normal fatty tissue , - benign disease, malignant transformation is exceptional
42
Progressive lipodystrophy | Barraquer–Simons syndrome
- rare form of acquired lipodystrophy - bilateral gradual symmetrical reduction of adipose tissue that begins at the face (by the disappearance of the Bichat’s bubble) and may variably progress to the neck, upper arms trunk and abdomen keeping intact the adipose tissue of the lower extremities associated with : autoimmune diseases in a minority of patients (systemic lupus erythematosus, autoimmune thyroiditis and/or metabolic diseases (Diabetes) - females are more affected than males - when it occurs in men, it occurs earlier
43
Insulin lipodystrophy
Abnormal reactions in subcutaneous fat to insulin - in diabetic patients
44
LIPOATROPHY is characterized by:
- subcutaneous nodules alternating with areas of adipose tissue atrophy - cutaneous hypoaesthesia, possibly - considered an adverse effect with an immune mechanism
45
LIPOHYPERTROPHY:
benign tumor like swelling of fatty tissue at the injection site secondary to lipogenic effect of insulin
46
Rothmann Makai Syndrome
- spontaneous paniculitis of children (very rare ) - A variant of lobular panniculitis presenting with numerous large subcutaneous lesions - small, circumscribed, tender, erythematous subcutaneous nodules or plaques, most frequently occurring on the extremities and less commonly on the trunk and face - with no severe systemic involvement - version: lipophagic panniculitis-characterized by atrophy in lesions with skin depressions
47
Weber-Christian Disease
- idiopathic nodular panniculitis, which is characterized by subcutaneous nodules: > symmetrical, size 1-2 cm, sensitive, erythema associated their disruption expresses a brown oily liquid (liquefying paniculitis) > characterised by exacerbations and remissions within a few weeks > it heals with depression of the overlying skin > lesions are bilaterally symmetrical and are usually seen in the lower limbs > systemic symptoms are associated: fever, asthenia, nausea, vomiting, weight loss, myalgias, arthralgias
48
Inflammatory disorders of the subcutaneous | tissue: cellulite and paniculitis
- inflammation without necrosis of the skin and subcutaneous tissue - redness, tumor, heat, pain (rubor, tumor, calor, dolor) - the skin entrance gate can sometimes be identified - severe infection is suggested by the presence of: - altered general condition, fever - regional lymphangitis - purplish bullous lesions circumferential disposition
49
Progressive hemifacial atrophy | Parry–Romberg syndrome (PRS)
1. progressive shrinkage and degeneration of the tissues beneath the skin, 2. usually on only one side of the face (hemifacial atrophy) 3. evolves self-limiting with residual and mutilating hemifacial atrophy 4. skin, subcutaneous tissue, underlying muscles, nerves, hair are affected 5. rare disease 6. higher prevalence in females