week 3 Flashcards

1
Q

primary vs secondary lesion

A

Primary lesion: initial lesion that has not been altered by trauma or manipulation, and has not regressed

Secondary lesion: develops as the disease evolves or as the patient damages the lesion i.e. rubbing, scratching, infections.

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2
Q

primary lesions > 1 cm

bulla

nodule

patch

plaque

A

Bulla: A circumscribed, elevated lesion that
measures ≥ 1 cm and contains serous or hemorrhagic fluid (i.e., a large blister)

Nodule: A palpable, solid, round ellipsoidal lesion measuring ≥ 1 cm; it differs from a plaque in that it is more substantive in its vertical dimension compared with its breadth.

Patch: A circumscribed, nonpalpable discolouration of the skin that measures ≥ 1 cm.

Plaque: A palpable, solid lesion that measures ≥ 1 cm.

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3
Q

primary lesions < 1cm

macule

papule

petechiae

vesicle

A

Macule: A circumscribed, nonpalpable discolouration of the skin that measures <1 cm in diameter.

Papule: An elevated, solid lesion that measures < 1 cm.

Petechiae: Nonblanching reddish macules representing extravascular deposits of blood, measuring ≤ 0.3 cm (less than the size of a pencil eraser).

Vesicle: A circumscribed, elevated lesion that measures <1 cm and contains serous or hemorrhagic fluid (i.e., a small blister).

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4
Q

wheal

pustule

purpura

A

Wheal: A round or annular (ring-like), edematous papule or plaque that is characteristically evanescent, disappearing within hours; may be surrounded by a flare or erythema (i.e., a hive)

Pustule: A lesion that contains pus; may be follicular (centered around a hair follicle) or nonfollicular.

Purpura: Nonblanching reddish macules or papules representing extravascular deposits of blood, measuring > 0.3 cm.

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5
Q

secondary lesions

atrophy

crust

erosion

lichenification

scale

scar

ulcer

A

Atrophy
A depression in the skin resulting from thinning of the epidermis, dermis and/or subcutaneous fat.

Crust
A collection of dried blood, serum, and/or cellular debris.

Erosion
A focal loss of epidermis does not penetrate below the dermal-epidermal junction and, therefore, can heal without scarring.

Lichenification
Thickening of the epidermis resulting from repeated rubbing, appearing as accentuation of the skin markings.

Scale
Excess dead epidermal cells; scale may be fine, silvery, greasy, desquamative, or adherent.

Scar
Abnormal formation of connective tissue, implying dermal damage.

Ulcer
A focal loss of full-thickness epidermis and partial to full-thickness dermis, which often heals with scarring

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6
Q

global reaction patterns

A

Papulosquamous eruptions (Papules and plaques with scale)

Folliculopapular eruptions (perifollicular papules)

Dermal reaction patterns

Purpura and petechiae

Nonpalpable purpura

Blistering disorders (vesicles, pustules and bullae)

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7
Q

history in derm

A

When? Onset
* Where? Site of onset
* Does it itch or hurt? Symptoms
* How has it spread (pattern of spread)? Evolution
* How have individual lesions changed? Evolution
* Provocative factors? Heat, cold, sun, exercise, travel history, drugs, pregnancy, seasonal changes
* Exposure(s) at the site? Changes to routines (laundry detergent, cosmetics, cleaning products etc.?
* Previous treatment(s) and response to Treatment: Topical and systemic
* Constitutional symptoms? Headaches, fever, chills, weakness, malaise arthralgias, etc.
* More chronic ones – weight loss, weakness, malaise

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8
Q

physical exam for derm

A

General shape: round, oval, polygonal, polycyclic, annular (ring-shaped), iris,
serpiginous (snakelike), umbilicated.
* Size
* Colour
* Margination
* Well defined
* Ill defined
* Palpation
* Consistency (soft, firm, hard, fluctuant, board-like)
* Deviation in temperature (hot, cold)
* Mobility
* Tenderness?
* Estimate the depth of the lesion (i.e. dermal or subcutaneous)
Number: Single or multiple lesions
Arrangement: Multiple lesions may be:
* Grouped: herpetiform, arciform, annular, reticulated (net-shaped), linear,
serpiginous
* Disseminated: scattered discrete lesions Confluence: Yes or no
Distribution:
* Isolated?
* Localized vs. regional vs. generalized
* Pattern: symmetric, exposed areas, sites of pressure, intertriginous area, follicular localization, random, following dermatomes or Blashko lines

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9
Q

ABCDEs for melanoma and dysplastic nevi (nevus)

A

asymmetry
irregular borders
variegated colour
diameter (>6mm)
evolution/ enlargement (change over time)

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10
Q

oblique vs subdued lighting

A

Oblique lighting: Used to view degrees of elevation or depression in a lesion. Done in a darkened room.

  • Subdued lighting: Used to enhance the contrast between circumscribed hypopigmented or hyperpigmented lesions and normal skin.
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11
Q

wood lamp in derm

A

to see different in colour and melanin pigments

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12
Q

diascopy vs dermascopy

A

Diascopy
* Firmly pressing a microscopic slide or glass spatula over a skin lesion.
* The examiner determined whether the red colour of a macule of papule is due to capillary dilatation (erythema) or due to extravasation of blood (purpura) that does not blanch.

Dermoscopy (also called epiluminescence microscopy)
* A hand lens with built-in lighting and a magnification of 10x to 30x is called a dermatoscope and allows for inspection of deeper layers of the epidermis and beyond. Helpful to distinguish between a benign and malignant lesion.
* These tools are typically used by dermatologists and not necessary in a naturopathic medical practice

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13
Q

patch testing vs prick testing

A

patch = allergic contact
prick= type 1 allergies; wheal appears

Patch testing
* Used to confirm a diagnosis of allergic contact sensitization and identify the agent that caused the allergic reaction.
* Substances to be tested are applied to the skin in shallow cups (Finn chambers), taped onto the skin and left in place for 24 – 48 hours. Contact hypersensitivity will show as a papular vesicular reaction that will develop within 48 to 72 hours when the test is read.

Prick testing
* Used to determine type I allergies
* A drop of a solution containing a small amount of the allergen is placed on
the skin and the skin is pierced through this drop with a needle.
* A positive result would be a wheal appearing within 20 minutes.
* Caution – the patient needs to be under constant supervision due to possibility of anaphylaxis.

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14
Q

skin scraping

what chemical is used?

A
  • Dermatophyte/KOH Collection
  • Microscopic examination for mycelia should be made of the roofs of vesicles or of scales or in the hair in dermatophytosis.
  • The tissue is cleared with 10 to 30% KOH and warmed gently. Hyphae and spores can then be viewed.
  • Microbiology (Culture and Sensitivity) and Specimen Handling Biopsy
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15
Q

biopsy

A

Biopsy
* Different tools can be used for different types of lesions
* Punch biopsy:
* Useful in the work-up of cutaneous neoplasms, pigmented lesions, inflammatory lesions and chronic skin disorders.
* 3 to 4 mm punch, a small tubular knife cuts through the epidermis, dermis and subcutaneous tissue by rotating the tool.
* Excisional biopsy (wide local excision)
* Surgical removal of a tumour and some normal tissue around it.

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16
Q

epidemiology of sebhorreic dermatitis

A

-males, babies or 40+
-hyperandrogenism
-stress
-cold weather
-immunosuppression
-zinc deficient

17
Q

what is sebhorreic dermatitis and its causes

A

-sebaceous gland inflammation
-androgen hormones, Malassezia yeast infection, altered immunologic response

18
Q

atopic dermatitis pathophysiology

Ig_?

A

-Allergic, inflammatory
-Epidermal barrier dysfunction
-Elevated IgE

19
Q

contact dermatitis pathophysiology

2 types;

type __ hypersensitive?

A

-erythema + pruritis from exogenous agent
1. irritant CD: chemical or physical abrasion (i.e. creams, alcohol, friction, temp)
2. allergic CD : delayed immunologic (type IV hypersensitivity)

20
Q

Dyshidrosis (acute palmoplantar eczema) pathophysiology

A

nonspecific immunologic reaction
-delayed hypersensitivity rxn
-acute spongiotic formation in epidermis of palmoplantar surfaces
-overexpress aquaporin (water and glycerol transport to epidermis)
-filaggrin mutations