Inflammatory Conditions and Nail Disorders Flashcards

1
Q

acne vulgaris

A

disease of sebaceous glands beginning at puberty

-present on face, neck, trunk

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2
Q

follicular thickening

A

hyperkeratosis and thickening of the hair follicle above sebaceous duct–> blockage vs. regular shedding

  • blockage= comedone
  • follicle ruptures into dermis–>inflammatory rxn–>papules, pustules, nodules, and cysts
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3
Q

sebum production

A
  • circulating androgens stimulate, estrogens can suppress
  • sebum formed by gland when cells of gland are broken down/converted into lipids
  • P. acnes, found on normal skin flora, produce lipase–>breaksdown triglycerides–>FFAs
  • FFAs are irritants and comedogenic
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4
Q

open comedomes

A
  • primary lesion

- blackheads (black from oxidation of tyrosine to melanin in follicular orifice

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5
Q

closed comedomes

A
  • primary lesion

- whiteheads

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6
Q

secondary lesions

A

scarring and pitting excoriations

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7
Q

associated findings of acne

A

pain or pruritis, emotional upset and depression

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8
Q

treatment of acne

  1. superficial acne
  2. deep acne
  3. both deep and superficial acne
A

multiple medications; address each patient individually, tailor plan to specific acne; promote good hygiene

  1. topical agents
  2. PO meds
  3. topical and PO meds
    - practice prevention, NOT spot tx
    - once breakout has happened, damage already done, stress pt education
    - if cannot get acne under control–>refer derm
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9
Q

nonpharmalogical tx

A
  • ensure compliance of pt with therapy
  • proper cleansing technique–>wash BID with facial cleanser
  • avoid face creams, cold creams, or any type of grease on face
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10
Q

tx for hormonal deep cystic acne

A

women only

  • spiranolactone 100 mg qday
  • low estrogen oral contraceptives
  • if abx and hormonal approaches fail–>accutane (isotretinoin)
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11
Q

tx of non-hormonal deep cystic acne

A

oral abx or accutane (if abx fail)

  • amoxicillin 500 mg BID
  • minocycline 100 mg BID
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12
Q

tx of surface red bumps and papules acne

A
  • topical abx–>clindamycin soln, lotion, or gel BID

- benzoyl peroxide agent

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13
Q

tx of comedones (black heads and white heads)

A

exfoliating/keratolytic agents: retina A, taxorac, differin qhs to qohs

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14
Q

isotretinoin: function and tx plan

side effects?

A
  • inhibits sebaceous gland function and keratinization
  • tx for 15-20 weeks, than an interval of 6 months, retreat as needed

side effects: teratogenic, hepatotoxic, extreme dry skin, hyperlipidemia

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15
Q

papules and pustules occurring on face often with ERYTHEMA, FLUSHING, and TELANGIECTASIAS

-age 40-70

A

rosacea

tx:
prevention: avoid ETOH, hot beverages etc. (redness)
Topical: metronidazole BID; clindamycin, erythromycin solt.
systemic: abx like acne–>tetracycline, minocycline, doxycycline

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16
Q
  • females>males
  • pruritus or burning
  • discrete or clustered, papules or pustules around the mouth, nasolabial folds
  • may become scaly or superinfected
A

perioral dermatitis

tx: wash gently with mild soap
- metronidazole (metrogel) qhs or BID
- discontinue steroid use
- oral abx: tetracycline 500 mg BID; minocycline 50-100 mg BID
- refer if persistent (patch testing for allergies)

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17
Q
  • inflammatory condition of apocrine gland
  • AUTOIMMUNE condition
  • lesions aseptic
  • part of follicular _____ _____
A
Hidradenitis Suppurativa
Occlusion Tetrad:
1. acne conglobata
2. pilonidal cyst
3. folliculitis decalvans
4. hidradenitis suppurativa

tx: oral abx (helps inflammation), humira

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18
Q

-one or more nails separated at the hyponycium
-signs of 2ndary infection
Etiology?
If all nails involved?

A

onycholysis: separation of nail from nail bed

Etiology: commonly idiopathic; systemic causes: psoriasis, eczema, tines, poor peripheral circulation

all nails involved: phototoxic rxn or thyrotoxicosis

tx: idiopathic–>resolves spontaneously
2ndary infection: may prevent reattachment
-keep nails clipped as short as possible to reduce further trauma

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19
Q
  • subungual hyperkeratosis, onycholysis, yellow-white in color
  • yellow streaks/yellow oncholytic areas in central portion of nail plate
A

onychomycosis

tx: oral meds (check LFTs)–>lamisil; 3 mo for fingernails and 4 mo toenails
- sporonax: pulse dosing x 3 months
topicals: pen-lac lacquer (Ciclopirox)–> tx for 6 months

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20
Q
  • horizontal trough across nail plate of all nails

- 3 months post-precipitating event

A

Beau’s lines

tx: patient reassurance–>deformity will grow out within 4 months

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21
Q
  • posterior nail fold feels spongy
  • nail becomes more curved
  • distal phalanx enlarges
A

clubbed nail/fingers

tx: important physical sign and cause should be saught-rarely noticed by patient
- pulmonary, CV, and miscellaneous etiologies

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22
Q

concavity of nails

A

Koilonychia
etiology: thinning and softening of nail plate; congenital cause, 2ndary to iron deficiency anemia, Reynaud’s, physical or chemical trauma

tx: treat underlying cause, nails usually return to normal

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23
Q

minute “pits” which occur in a random or uniform pattern across nail plate
-usually all nails affected

A

pitted nails

etiology: inflammatory skin conditions–> psoriasis, alopecia areata, atopic dermatitis 2ndary to parakeratosis

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24
Q

longitudinal depression in the nail

A

habit tic- habitually stroking top of thumb nail

  • can be associated with anxiety
    tx: behavioral modification, occlusion of nail preventing occurrence
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25
white spots on nails
leukonychia- common complaint etiology: 2ndary to nail trauma - NO association with Ca deficiency
26
red or brown pigmented, linear, splinter-like lesions
splinter hemorrhages: tiny subungual hemorrhages etiology: most commonly trauma, can be associated with SLE, endocarditis
27
brown nails
nail hyperpigmentation etiology: most commonly from dyes (textile workers), nicotine, or other meds
28
splitting of nail into its component layers
lamellar nail dystrophy etiology: 2ndary to repeated wetting and drying out of nails tx: reassurance! reinforce gloves while immersing nails in water
29
proximal 2/3 of nail plate is white and the distal 1/3 normal pink nail bed
Terry's nails: rare etiology: CHF, hypoalbuminemia
30
malignant melanoma vs. nail trauma
inspect nail fold for Hutchinson's sign: black discoloration of proximal nail fold at base of pigmented streak = melanoma
31
abnormal, delayed rxn to sunlight exposure
polymorphic light eruption-->1st exposure to sun of the year-->autoimmune tx: mid-potency topical steroids
32
- erythema and blistering of hand | - common with travelers to tropical destinations drinking citrus drinks
phytophotodermatitis: cutaneous phototoxic inflammatory eruption
33
common inducers of drug-induced photosensitivity
tetracyclines, fluoroquinolones, NSAIDs, diuretics, retinoids (counsel pts when putting them on these meds)
34
drug eruption: skin sxs, labs, txs.
-can mimic a wide range of dermatoses skin sxs: morbilliform, urticarial, papulosquamous, pustular, and bullous labs: CBC, CMP, ANA, punch biopsy tx: DISCONTINUE drug - antihistamines for pruritus and urticaria - epi for emergency - corticosteroids for severe cases
35
a drug eruption can turn into? skin sxs? labs? tx?
erythema multiforme: acute, self-limited, and sometimes recurrant type IV hypersensitivity reaction skin sxs: lesion development over 10 days; macule-->papule-->vesicle-->bullae in center of papule, dull redness, TARGETOID LESIONS labs: HSV viral cx if indicated, biopsy to confirm dx tx: drug discontinuation; oral acyclovir; severe cases: prednisone
36
erythema multiforme drug causes infection causes other
drug: sulfonamides, phenytoin, barbiturates, penicillin, allopurinol infection: s/p HSV infections, mycoplasma - idiopathic
37
- generalized pruritis precede rash by several days | - severe mucocutaneous papules/vesicles develop to desquamation
-steven-johnson syndrome (<10% epidermal detachment) | -toxic epidermal necrolysis >30% detachment
38
steven-johnson syndrome/toxic epidermal necrolysis Causes: 1. drugs 2. genetic factors 3. infectious causes
1. phenytoin, barbiturates, valproic acid, carbamazepine, sulfur derivatives (bactrim) 2. HLA antigens 3. HSV, HIV, coxsackie, influenza, hepatitis
39
steven-johnson syndrome/toxic epidermal necrolysis 1. describe general sxs: prodrome vs. syndrome 2. labs 3. tx
1. prodrome: cough, HA, malaise, arthralgias Syndrome: inflammation and desquamation of oral mucosa, esophagus, pharynx, larynx, anus, vagina, urethra, sometimes severe ocular sxs 2. TNF-alpha, IL-2, IL-6, CRP, biopsy 3. agent withdrawal (if drug induced); admission; oral/IV prednisone; fluid management
40
- large 3.0-20 cm deep seated subcutaneous nodules - only appreciated on palpation - bilateral on pretibial surfaces, possibly knees/arms, rarely face/neck - usually in women and due to oral contraceptives
erythema nodosum- inflammation in fat tx: tx underlying condition - when symptomatic: bedrest or compression stocking - NSAIDs, salicylates for 2-4 wks - systemic steroids (when you know cause and infections are excluded)
41
- present for < 30 days | - large, transient wheals
acute urticaria antihistamines, avoid triggers
42
large transient wheals for >30 days
antihistamines, mast cell stabilizers, and prednisone
43
direct pressure on the skin-->urticaria secondary to an exaggerated response of the skin to trauma resulting in histamine release from mast cells
dermatographism condition ultimately resolves, but can take yrs
44
ordinary urticarial swellings that are more paindul and pruritic after prolonged pressure
pressure urticaria recovery spontaneous
45
same as urticaria except involves the deep dermis and subQ tissue
angioedema
46
dermal papules and annular plaques
granuloma annular tx: topical vs. intralesional steroids
47
- velvet-like hyperkeratosis - insulin-induced - most common on peripheral neck and flexural areas
acanthosis nigricans tx: keratolytics
48
cholesterol deposition at medial canthus/upper eyelids
xanthelesma not easily treated
49
- NON-blanchable small-vessel vasculitis - RA, IBD, SLE have been implicated - skin often asymptomatic, pts may report itching, burning, pain
hypersensitivity vasculitis tx: underlying condition if one is determined leg elevation and compression
50
-descending vasculitis, usually after a strep infection
Henoch-Schoenlein Purpura tx: abx if followed bacterial infection
51
irregular plaques and patches of orange-brown pigmentation on lower limbs
Schaumberg's disease | tx: none, leg elevation and compression can slow progression
52
-lesions feel "wooden"
morphea -localized collagen deposition tx: often self-limited; topical steroids
53
- chronic inflammatory condition mostly affecting genital areas - can obliterate vaginal structures-->atrophy and band-like sxs
lichen sclerosis tx: high potency topical steroids and refer to OBGYN
54
autoimmune-mediated depigmentation
vitiligo tx: if lesions <6 mo old, can usually re-pigment using topical steroids or protopic ointment
55
grouped excoriations, urticarial plaques, papules, and vesicles on the extensor surfaces of elbows, knees, buttocks, and back
dermatitis herpetiformis tx: gluten avoidance-->improvement of skin sxs can take several months [autoimmune blistering disorder assoc. w/ gluten-sensitive enteropathy]
56
erythmatous, papular, urticarial lesions-->bullae form - bullae are large, tense, firm-topped oval or round lesions - mucous membrane not involved - (+) nikolski sign
bullous pemphigoid tx: PO/IV prednisone; azathioprine
57
oral lesions-->sole sign for months before other lesions arise -skin: flaccid blister with painful affected skin
pemphigous vulgaris tx: coricosteroids- long term - sulfasalazine
58
erythematous, confluent, macular BUTTERFLY eruption (MALAR rash) with fine scaling, erosions, and crust
systemic lupus erythematosus tx: depends on severity - hydrochloroqine
59
localized loss of hair in round or oval patches WITHOUT skin inflammation -exclamation point hairs
alopecia areata [possible autoimmune process due to association with other autoimmune diseases] tx: no curative process; palliative for cosmesis - psychological support - tx underlying disease - tx options: intralesional/topical steroid, UVA therapy
60
autoimmune hair loss with signs starting before age 40; can only affect scalp hair vs. affecting all scalp and body hair
alopecia totalis/universalis starts as alopecia areata and progresses to diffuse lose tx: none successful, only for early stage of alopecia areata
61
- daily dramatic hair shedding | - preceding traumatic event 6-16 wks prior to hair loss
``` telogen effluvium (think beau lines) -regrows in 4-6/12 months ``` Tx: reassurance!!