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160 Cards in this Set

  • Front
  • Back
locations of impetigo
face, hands, genitalia, scalp
superficial bullae, vesicles w/ turbid fluid, golden-crusted erosions

possible pruritus
impetigo
ecthyma, location and healing process
deep impetigo
legs
heals with scars
complications of impetigo
post-streptococcal glomerulonephritis
- RARE

not caused by staphylococcus impetigo
RX for impetigo
remove crusts
wash lesions
topical antibiotics (mupirocin)
systemic antibiotics
small, dome-shaped, yellow pustules on a red base, hair shaft in center lesion
Bockhart's impetigo
-aka superficial folliculitis
Bockhart's impetigo location, etiology, treatment
children- scalp, face, buttocks, extremities
S. aureus
RX: gentle cleansing, topical antibiotics, occasionally systemic antibiotics
florid appearance
superinfection in acne patients on long term systemic antibiotics
Gram-negative folliculitis
-Klebsiella, Enterobacter, Proteus
Rx: oral antibiotics, Retinoids
Folliculitis barbae (sycosis barbae)
deep-seated folliculitis of bearded area
Staph origin
Rx: topical or oral antibiotics
central necrosis and suppuration- deep, red, tender nodules
Painful, circumscribed, perifollicular
Staph abscess --> Furuncles
extreme pain, constitutional symptoms
deep-seated staph abscesses
interconnected furuncles = carbuncle
men
back of neck, shoulders, buttocks, hip joint and thighs
deeper subcutaneous tissue, acute suppurative inflamation

diffuse redness, swelling, tenderness
Cellulitis
- complication of wound or trauma
- Staph aureus> Group A strep
non-sharply defined/elevated borders
VS
well demarcated border
Cellulitis
VS
Erysipelas (more superficial)
- Group A strep, face
Corynebacterium minitussimum
Erythrasma
superficial bacterial infection
reddish brown, slightly scaly to smooth, shiny patches

groin and axillae
toe webs- maceration and scaling
Erythrasma
obese, diabetic, debilitated pt

Wood's lamp exam: coral red fluorescence
Erythrasma

rx: topical or oral antibiotics (erythromycin)
papillomavirus causing intraepidermal tumor
warts
sessile lesions, on fingers
raised, rough gray surface
verruca vulgaris
face and neck
looks like a skin tag
filiform, digitate warts
fingerlike projections
slightly elevated papules
may have just a few, or several hundred
smooth, flesh-colored to tan/brown
flat warts
fleshy warts, around mucocutaneous junctions and intertriginous areas

pedunculated or polypoid nodules
condylomata acuminata aka genital warts
associated with cervical or penile carcinomas
condylomata acuminata
grouped vesicles on erythematous base
primary and recurrent infection (pain and burning- triggers: fv, trauma, sunlight, stress)
HSV

Dx: Tzanck smear- multi-nucleated giant cells, viral culture!
erythematous macules, clear vesicles, then pustules and rupturing with crust formation

mutliple lesions stages present at one time
Varicella-Zoster virus

- spread: respiratory route
mostly epidermal changes
may be: macules, patches, papules, plaques
scales are present
sharp marginatinos
papulosquamos disorders
large oval patch, then multiple lesions in symmetrica long asix distribution along lines of cleavage on trunk and proximal extremities
(pruritis w/ onset)
pityriasis rosea
possible pregnancy complications
especially first trimester infection
pityriasis rosea
important to exclude syphilis
(see rash on palms, soles, mucous membranes and shotty adenopathy)
pityriasis rosea
treatment for pityriasis rosea
none necessary
- topical creams, steroids, anti-itch, immunomodulators
PO erythromycin 2-3 weeks
UVB/sunshine
post streptococcal upper respiratory infection, kids/adolescents
guttate psoriasis
post steroid withdrawal + fever + arthalgias

mucous membrane involvement- erythema with sheets of small pustules
generalized pustular psoriasis
Psoriasis:

genetic aspect?
T cell driven?
related cytokine and chemokine pathways?
ICAM-1 and E-selectin on vascular endothelial cells?
YES
relation to crohn's, ulcerative colitis, sacroiliitis, forms of arthritis (variety of manifestations), cardiovascular diseases, HLA-B27
Psoriasis
Bowen's disease
squamos cell carcinoma in situ
-ulcerated surface
localized chronic eczema
lichenified, excoriated skin
urethritis, arthritis, conjunctivitis (mucocutaneous lesions)

psoriasiform skin lesions
Reiter's disease
most often seen in men
rx for cutaneous lesions of psoriasis
emolliation
topical steroids (strength variation depending on skin area and plaque resistances)

sunlight, UVB

NEVER use systemic steroids (disease may worsen when dose lowered, may precipitate pustular psoriasis)
possible development of squamos cell carcinoma
oral ulcerated lichen planus
lichenified skin, excoriations
localized neurodermatitis
uniform, pinhead-sized flesh colored papules

asymptomatic or mildly prurits
lichen nitidus

upper extremities, chest/abdomen, glans penis

self limited
linear eruptions of scaly patches
arms and upper trunk
appear 2-3 weeks
lichen striatus

possible infections trigger

self limited
fine white lacy lines on papules

papules - flat topped, purple, polygonal

lacy reticulated pattern on mucous membranes

VERY ITCHY
whickham's striae

Lichen planus

mucous membranes: mouth, penis, vagina
thinning, longitudinal ridging of nails, subungal hyperkeratosis - lifting distal nail plate, pterygium formation
Lichen planus
Psoriasis, Lichen Planus, Lichen nitidus
Koebner phenomenon
30 year old, with + family history
verrucous surface, hyperpigmented
Seborrheic Keratosis
Dermatosis Papulosa Nigra
small seborrheic keratosis
malar area, darker individuals
rapid, widespread seborrheic keratosis
associated internal malignancy

Sign of Lesar-Trelat
middle aged person

fleshy, papillomatous skin lesion on areas of skin that rub together
Acrochordon- Skin tag
(neck, axilla, inguinal folds, under breasts, waist/bra-line)

multiple- may have systemic associations
possible link to Seborrheic keratosis
middle aged woman, with lesion on extremities
possible relation to trauma
reddish-brown, firm papule, dimple sign on compression
dermatofibroma
if painful or compressing vital organs- require surgery

small, firm, flesh-colored papules
Neurofibroma
Von Recklinghausen's disease
multiple neurofibromas + internal neurofibromas + cafe-au-lait spots
male with acne history, who picked at his lesions leading to infection/inflammation
develops dermal nodule w/ central puncta, that may express cheesy material
Epidermal Inclusion Cyst/Sebaceous Cyst

rx: surgical excision, intralesional kenalog
Gardner's syndrome
multiple epidermal inclusion cysts, colon polyps, osteomas, fibromas
looks just like epidermal cyst but involves a hair follicle, on scalp or face
pilar cyst

benign, remove everything, all epidermal lining
white or yellow, small papule (<3mm), often multiple
Milium

no required therapy (incise, express)
childhood lentigines
congenital syndromes- multiple organ system defects
associated with vitiligo and malignant melanoma (especially when present in adults)
halo nevus

hypopigmented area around junctional nevus

requires good skin checks
most melanomas arise from melanocytic nevi
false,
most melanomas arise de novo
familial dysplastic nevus syndrome
multiple unusual looking moles, develops melanoma
60-70 year old fair skinned lady who use to love to tan

pearly papules/nodules w/ telangiectasias
rolled pearly borders
Basal cell carcinoma

slow growing, locally invasive

rx: curettage/electrodesiccation, surgical excision, or Mohs
re-check q3-6 months
Nodulo-ulcerative basal cell carcinoma
pearly, telangiectatic papule/nodule
frequently ulcerates
superficial basal cell carcinoma
red, microulcerative macule
white-yellow, poorly defined skin color
telangiectatic macule/plaque
morphea/infiltrative basal cell carcinoma
imiquimod
topical immune modulator

actinic keratoses
superficial basal cell carcinoma
pre-cancerous lesion of keratinocytes
actinic keratosis
rough, sandpaper feel
on sun-damaged skin
actinic keratosis
-hyperkeratotic papules on erythematous base
potential devo to squamos cell carcinoma if untreated
actinic keratois
-hyperkeratotic papules on erythematous base
in situ SCC

pt exposed to arsenic

erythematous, slightly scaly plaque, occasional ulceration
Bowen's Disease

-possible increased internal malignancy
elderly person with previous large amount of sunlight exposure

hyperkeratotic or ulcerative
Squamous Cell Carcinoma

rx: curettage/electrodesiccation, excision w/ permanent/frozen section control, Mohs surgery, RT
spreading of Squamos Cell carcinoma
local lymph nodes, liver, lung, bone, brain
perineurally
Well differentiated SCC, sudden onset/rapid growth

rarely malignant
Keratoacanthoma

possible spontaneous regression
tumor with central crater or keratinous plug
often telagiectasias
Keratoacanthoma

rx: isotretinoin
fibroblast tumor that may accelerate during pregnancy
red-brown infiltrative nodules
Dermatofibroma Sarcoma Protuberans
ABCDE, U
Melanoma
clinical signs:
Asymmetry, Border (irregular/notched), Color, Diameter (>1 cm), Evolution/Change, Ulceration
also check for diffusion of pigment in surrounding normal skin
65yo+, sun-exposed skin damage

slowing growing melanoma in situ, should be removed
Lentigo Maligna
- irregular brown macule
- Hutchinson's Freckle
invasive melanoma component, similar to hutchinson's freckle
lentigo maligna melanoma
30-50 yo
male- flat lesion w/ nodules, pigmented on back
female- same but on posterior thigh

most common clinical variant of melanoma
Superficial spreading melanoma
most common melanoma in dark skinned people

found late, poor prognosis
Acral-lentiginous melanoma
most important indicator of prognosis for melanoma
Breslow's thickness
what to do with a suspicious melanoma lesion
BIOPSY w/in a week- time is life w/ melanoma
- local- depth, aggressiveness, clear margins
- sentinal node biopsy
chemo/removal if mets
immunotherapy
effects of blocking COX-1
gastric ulcers, perforations, GI bleeds

And anti-thrombolytic effect
- impairs platelet function
- why aspirin is given to pts at CVD risk
effects of blocking COX-2
COX-2 is inducible and inflammatory (as opposed to COX-1 which is constituitive and protective)

antipyretic, analgesic, anti-inflammatory
benefits of NSAIDs when treating Rheumatoid Arthritis
reduce pain/inflammation, improve motility, slow/arrest tissue damage

possible inhibition of PMN adhesion

also use NSAIDs: OA, acute gouty arthritis, SLE, spondyloarthropathies
Coxibs
signs and symptoms of RA and OA

preferential inhibition of COX-2
with newer generations, increasing COX-2 selectivity, but drastic GI (perforation, ulceration, bleeds) and heart (MI, stroke) side effects
adverse effects of coxibs
GI: perforation, bleeding, ulceration
(PUBs)

CV: MI, stroke
special property of aspirin
covalently acetylates COX-1,2
- works for the life of the platelet
- no functioning enzyme present until the cell makes a new one
- COX-1 - stops platelet aggregation--> anti-thrombolytic effect
what drug levels are increased by either aspirin or celecoxib
warfarin!
Salicylic acid
NSAID
reversible inhibition of COX
peripheral COX inhibition
acetominophen
uses of acetominophen
infection related fever, pain, aches
- analgesic, antipyretic

NO anti-inflammatory effects
what effect that aspirin has is acetominophen lacking?
anti-inflammatory
what's the big concern with tylenol use
overdose~ at 20X the therapeutic level (lower in alcoholics whose damaged livers can't handle the same load)

- no signs for first 24 hrs
- then N/V, anorexia, ab pain, detectable LFTs
- 2-5 days- devo jaundice and bleeding
- at day 5- either spontaneously heal, or require liver transplant!
what's the antidote to tylenol overdose?

and what does it do
mucomyst
- replaces glutothione
given oral or IV
what happens if you give aspirin to kids, especially post febrile viral illness
Reye's syndrome:
brain and liver effected - possibly fatal
aspirin overdose
CNS stimulant and depressant
- increase respiration: respiratory alkalosis
- decrease respiration: respiratory acidosis

requires cardiovascular and respiratory support, and sodium bicarbonate
what can you give when salicylates (ie aspirin) are no longer tolerated/effective?
indomethacin, ibuprofen (advil)
indomethacin stronger or weaker than tylenol?
stronger

but toxicity (GI and CNS) sufficient to NOT use for simple analgesia/antipyretic action- use tylenol instead
if pt can't take aspirin, and have an acute attack of gouty arthritis or ankylosing spondylitis, what do you give?
indomethacin (primarily anti-inflammatory)
which has worse side effect profile?
- indomethacin
- advil/ibuprofen
indomethacin: GI and CNS
advil: nausea, heartburn, epigastric pain
- RA, DJD (has anti-pyretic,analgesic and anti-inflammatory properties)
when would you want to use aleve/naproxen
longer half life than advil and indomethacin

use with PPI
name the one drug that can be given parenterally, and is a potent non-narcotic analgesic?
Ketorolac
two major NSAID AE that should be watched out for?
SKIN: Stevens-Johnson
RENAL: AIN, acute papillary necrosis
which rheumatic disease due you prescribe an NSAID for?
Gouty arthritis, RA, OA, SLE, spondyloarthropathies
what is conservative treatment of rheumatoid arthritis?
rest, proper diet, physical therapy, NSAIDs
list the NSAIDS
Salicylates/Aspirin
Para-Aminophenol: Acetaminophen (tylenol)
Indomethacin and Ibuprofen (advil)
Ketorolac
Coxibs- selective NSAIDs
young female
palpable purpuric lesions after taking penicillin

biopsy: dermal blood vessel shows PMNs in walls, fibrin in/around the vessel, nuclear fragments from dead PMNs.
Extravasated RBCs in dermis and epidermis
leukocytoclastic vasculitis
- hypersensitivity vasculitis
which is the more locally invasive form of basal cell carcinoma?
sclerosing > multifocal superficial or nodular
57 yo, male construction worker
mass developed 2 years ago
PMHx: roughened scaly lesions on arms/face were frozen off

what were the lesions? what does he have now?
actinic keratosis (parakeratosis, cytologic atypica/dysplasia, basophilic degeneration)

current tumor: Squamous cell carcinoma
which has higher metastatic potential:
SCC de novo or one that developed from previous actinic keratosis?
de novo
70 year old seaman
head lesion: dark, variable pigmentation and irregular borders
what does he have?
melanoma!!!
what neoplasm most commonly occurs in sun exposed skin?
basal cell carcinoma
clinically, how to id junctional nevi from compound and intradermal
junctional nevi: macular
compound and intradermal nevi: papular

intradermal- flesh colored
junctional and compound: pigmented
pts with family history of melanoma who have dysplastic nevi have increased risk of developing melanoma even in clinically unaffected skin. T/F
T
how do you measure breslow's thickness?
from granular layer to deepest aspect of melanoma
<.85 mm- low malignant potential
> 4 mm
in which disease does serum antibody level correlate with disease activity?
- pemphigus vulgaris
- bullous pemphigoid
pemphigus vulgaris
17 yo male, increasing pain in left knee
- no limitation of movement or soft tissue mass

Labs: increased alkaline phosphatase
Bone scan: increased uptake in left knee region

radiograph: dense lesion in distal femural metaphyseal region, extending into anterior and posterior cortices and epiphysis
osteosarcoma (mostly present in metaphyse=is)
what bone lesions can yield increase uptake on a bone scan?
osteomyelitis (infection)
fracture with callus formatin (possible trauma?)
Osteosarcoma
most common primary malignant tumor of the bone
osteosarcoma
- characteristically osteoblastic/osteosclerotic
where are ewing's tumors located?
diaphyseal region of bone
what is codman's triangle?
frequently noted in osteosarcomas
triangle center contains reactive bone
- borders are:
- cortical bone, periosteum, tumor
most common soft tissue tumor of adulthood
lipoma

- round, regular borders, no ulceration of skin, soft, not painful palpatation, freely moveable
located in: subcutaneous/adipose tissue
68 yo male, increasing mass in right thigh
no pain or limitation of motion

resected lesion: large, adipose tissue, myxoid/mucoid appearance, intralesional hemorrhage, invades skeletal muscle
micro: lipoblasts near arborizing vascular network
myxoid liposarcoma
- chicken-wire pattern of vasculature
- must be adequately excised to avoid recurrence

as cellularity increases, so does level of aggression (mets and recurrence)
young pt with nodule on forearm/chest/back

biopsy: myofibroblast like, w/ extracellular mucinous production
sharply demarcated, pushing but not invading or destroying surrounding tissue
nodular fasciitis

- reactive fibroblast tumor
fibroblast tumor that can be superficial (palmar, plantar) or deep (abdominal), hard to id margins

no mets, but can be fatal due to invasion and obstruction
fibromatosis

- fibroblastic proliferation- hypercellular scar like
most common soft tissue tumor in adults (40-60 yo)
malignant fibrous histiocytoma (extremities and retroperitoneum)
liposarcoma (deep tissues of thigh and retroperitoneum)
adult female with lots of pain, discomfort in lower abdomen area
leiomyoma
- smooth muscle tumor or uterine wall
very common
fibroblasts in storiform pattern: hurricane like, spins out from the center
benign vs maligant fibrous histiocytoma
benign vs maligant fibrous histiocytoma
benign: dermis or subcutaneous, pushing stellate border, excise wide border to avoid recurrence

malignant: cellular pleomorphism, multinucleate cells, atypical mitosis
- Mets and local recurrence- very likely!
30-60 yo
presents with sudden shoulder pain
xray shows: periarticular deposits
Basic Calcium Phosphate deposits
-hydroxyapatite
- NOT birefringent
degeneration of joints and tendons
- large joint destruction
calcific bursitis and tendonitis = painful!
- proliferative synovitis
- tendon erosion
BCP- hydroxyapatite

NSAIDs/corticosteroids- acute
surgery- large deposits impinging on joint
majority of pts with gout have hyperuricemia b/c?
decreased urate excretion
decreased renal clearance
- thiazides, alcohol intake/lactic acidosis (metabolic acidosis), respiratory acidosis
-thyroid disorders
excess urate synthesis causes?
how is this identified?
PRPP synthetase - increases de novo pathway
HGPRT - decreased re-utilization via salvage pathway
increased breakdown of nuclei acids (myeloproliferative disorders)
excess meat consumption
alcohol intake (increases ATP breakdown)

Urine urate levels: >800-1000mg/24hrs
arthritis incredibly prevalent in individuals above 85 years old
F> M
can mimic a variety of other forms of arthritis (gout, RA, OA), or asymptomatic
Pseudogout (calcium pyrophosphate dihydrate)
Diagnosis of Pseudogout
+Birefringent crystals, rhomboid/rectangular

Xray- calcification of cartilage = chondrocalcinosis

most prevalent in knee joint
Negative birefringent crystals, needle shaped
Monosodium urate, gout
- monoarticular:
first metatarsophalangeal joint
tarsus
knee, ankle
- inflammation develops w/in 24hrs
- erythema over joint
- Xray- asymmetric swelling of joint, soft tissue swelling
Factors associated with hyperuricemia
HTN, increased body weight, atherosclerosis, DM, hyperlipidemia
Treatment for chronic tophaceous gout?
Febuxostate> allopurinol
- handled by liver, not kidney, therefore easier to dose
- xanthine oxidase inhibitor

NSAIDs, corticosteriods, colchicine
X-ray shows rat bite, over-hanging edge
erosions from tophi- Gout
ILD, arthritis, Raynauld's
overlap syndrome of Polyomyositis
auto-antibody: Jo-1
treatment for PM/DM
corticosteroids- muscle strength recovers in 2-3 months
IVIG- for severe rash
severe- chemo drugs or cyclosporin

avoid sunlight
prevent osteoporosis
Lung findings in scleroderma
ILD
Pulmonary hypertension- extra P2
Fibrosing alveolitis, encases entire lung
dx: xray shows bilateral basilar fibrosis

rx: early!! w/ steroids/cyclophosphamide
CREST syndrome
limited type of scleroderma
anti-centromere antibody
Calcinosis
Raynauld's
Esophagial dysmotility/dysphagia
Sclerodactyly
Telangiactasia (face, lips, down GI tract)
anti-Scl 70
antibody against topoisomerase I
diffuse form of scleroderma
skin findings of Dermatomyositis
Periorbital edema
Gottron's papules (reddish-white shiny lesions over joints)
telangiectasias of nailbed
sunsensitive rash - face, chest, extensors (shawl distribution)
EMG findings in PM/DM
spontaneous, bizarre, polyphasic
fibrillation and sharp positive waves
highest contributing factor to mortality in Scleroderma pt
Renal involvement- intimal fibrosis in small renal arteries --> cortical hemorrhages, malignant HTN
- strokes and renal failure
- ACEI- MUST control BP
disease with increased osteoblast and osteoclast activity
increased vascularity
Paget's
pumice bone- susceptible to fracture

mosaic bone pattern from haphazard osteoclast resorption and then laying down of new bone by osteoblasts
Paget's
increased blood supply to affected bone --> leading to high output cardiac failure
Paget's
bone disease with increased risk of osteosarcoma development
Paget's
diseases with increased osteoclastic activity
osteoporosis
paget's disease
hyperparathyroidism- osteitis fibrosis cystica
thin, poorly formed bone
multiple fractures
blue sclerae
loose jointedness
osteogenesis imperfecta
osteoblast failure- inability to make type I collagen --> can't form trabeculae, therefore no woven bone
osteogenesis imperfecta
Bone disease where bone marrow transplant is curative
Osteopetrosis
- defect due to osteoclast failure
- sclerosis (thickened cortex) --> marrow cavity filing, visual disturbances, deafness, CN palsy, hydrocephalus
- bones brittle and subject to fracture
treatment for atopic dermatitis
enhance water content of skin and control pruritus
- avoid soaps and water
- topical steroids
- anti-histamines
- Moisturize
- UV light
uveitis, aortitis (aortic insufficiency), upper lobe fibrosis (and rigidity of chest wall)
additional signs of Ankylosing Spondylitis

- sacroiliac joints- narrow/obliterated joint space- fused joints
- longitudinal ligaments of spine calcified, fusion of vertebrae
urethritis- dysuria
conjunctivitis/mucocutaneous lesions
arthritis (periarticular structures)- achille's tendon, heal spur, sacroilitis
Reiter's

- US: chlamydia
- developing countries: diarrhea (C. jejuni)
insidious low back/gluteal pain
lasting longer than 3 months
Ankylosing spondylitis
in which rheum diseases is kidney involvement the major cause of mortality?
scleroderma, SLE
myocardial fibrosis, cardiomyopathy
EKG: RBBB, LAH
PM/DM