Nicholas Satterfield MD Emergency Medicine PGY2 Henry Ford Hospital Define dermatologic terms Discuss the approach to dermatologic complaints Discuss dermatologic diseases with high morbidity and mortality ID: 775094
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Emergency Dermatology: What You Don’t Know Can Kill
Nicholas Satterfield MD
Emergency Medicine PGY2
Henry Ford Hospital
Slide2Slide3Define dermatologic termsDiscuss the approach to dermatologic complaintsDiscuss dermatologic diseases with high morbidity and mortality
Objectives
Slide4Skin Anatomy
Slide5Flat lesionsMacule (< 0.5 cm)Patch (> 0.5 cm)
Derm Terms
Slide6Elevated LesionsPapule (Up to 0.5 cm)Plaque (Greater than 0.5 cm)Nodule ( Papule but deeper, involves dermis and sometimes subcutaneous tissue)
Derm Terms
Slide7Fluid FilledVesicles (Up to 0.5 cm)Bullae (Greater than 0.5 cm)Pustules (Vesicle but with pus)
Derm Terms
Slide8Blood derived (From leakage of capillaries)Petechiae (Less than 0.5 cm)Purpura (Greater than 0.5 cm)
Derm Terms
Slide9Erosion (loss of epidermis)Excoriation (itching leading to loss of epidermis)
Derm Terms: Secondary Changes
Slide10Ulceration (Loss of epidermis and dermis)
Derm Terms:Secondary Changes
Slide11Crusting (Collection of dried serum and cellular debris)
Derm Terms: Secondary Changes
Slide12Lichenification (Thickened epidermis)
Derm Terms: Secondary Changes
Slide13Atrophy (Thinning of epidermis or dermis)
Derm Terms: Secondary Changes
Slide14Scaling (Shedding excess dead epidermal cells by keratinization and shedding)
Derm Terms: Secondary Changes
Slide15Which would you rather have?
Slide16Approach
Slide17Slide18Slide19Slide20Slide21Slide22Early Meningococcemia, RMSF, TSS, EM, SLE, viral
exanthemLyme
Meningococcemia, RMSF, HSP, Vasculitis, SLE, ITP, TTP, rubella, EBV, Endocarditis
Secondary Syphillis, Anthrax
Necrotizing fasciitis, TSS, STSS, SSSS, Kawasaki, EM, hypersensitivity reactions, cellulitis, viral exanthem
EM, Stevens-Johnson, TEN, Pemphigus vulgaris, varicella zoster, HSV, necrotizing fasciitis (late)
Bacterial
folliculitis
, gonorrhea,
cellulitis
Slide23Which would you rather have?
Slide24Timing and progressionLocationChanges over timeTravelPMHOccupationMedications
History
Slide25Fevers (Rocky mountain spotted fever, toxic shock syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, Kawasaki Disease)Very Young (Meningococcemia, Kawasaki disease)Elderly (Meningococcemia, pemphigus vulgaris, meningococcemia, toxic epidermal necrolysis, Stevens-Johnson syndrome)Toxic Appearing (Necrotizing fascitis, meningococcemia, toxic epidermal necrolysis, Stevens-Johnson syndrome, toxic shock syndrome, rocky mountain spotted fever)Immunocompromised (Meningococcemia, herpes zoster, necrotizing fascitis)
Red Flags
Slide26Diffuse Erythroderma (Staphyloccocal scalded skin syndrome, toxic shock syndrome, streptococcal toxic shock syndromePetechiae/Purpura (Meningococcemia, necrotizing fascitis, vasculitis, DOC, rocky mountain spotted fever)Mucosa/Oral Lesions (Erythema multiforme major, toxic epidermal necrolysis, Stevens-Johnson syndrome, pemphigus vulagaris)Severe pain or tenderness (Necrotizing fascitis)Recent new drug use (Erythema multiforme, toxic epidermal necrolysis, Stevens-Johnson SyndromeArthralgias (Rocky mountain spotted fever, viral illness)
Red Flags Continued
Slide27Putting it together
Slide28Slide29PathologyAcute inflammatory condition leading to maculopapular rashBelieved to be due to immune complex depositionHas multiple etiologiesInfectious (HSV or mycoplasm most common)Drugs (Penicillins, sulfonamides, dilantin, barbituates)
Erthema
Multiforme
Slide30Prodrome of malaise, fever, arthralgiaDusky red papules with sudden appearance that as they enlarge the central area pecomes cyanotic and dustyTend to develop on palm, soles, extensor surfaces (knees and elbows)If due to drug reaction it tends to appearLesions may develop for 2-4 weeks then resolve in 1-2 weeksRarely can have a recurrent form or persistent form that is usually from HSV infection
Slide31Major includes one area of mucosal involvementMost common is oral (up to 70%) erythema, erosions or bullaeCan also have ocular bullae, pseudomembranes and purulent discharge (10-20%) which can lead to keratitis conjunctival scarring and visual impairment
Minor vs Major
Slide32If you suspect drug reaction stop the drugSupportive (NSAIDS, antihistamines)Kenalog (triamcinolone) 0.1% cream for non face and genitalsHydrocortisone 1% cream for face and genitalsLidex (fluocinonide) 0.05% gel for oral lesionsMagic mouth wash (2% viscous lidocaine, benadryl and maalox)Steroids?Rosens suggests to use if on trunk, EM Major and immunosuppressed If so start at 40-60 mg/daily with 2-3 week taperDermatology referralOptho referral: topical steroids and antibiotics
Treatment
Slide33SJS
TEN
Slide34PathologyAltered drug metabolism and immune complex mediated reactionEtiologyMedicationsInfection (Mycoplasma pneumonia, CMV)
Stevens-Johnson Syndrome and Toxic Epidermal
Necrolysis
Slide35Slide36Slide37Risk Factors
HIV
Genetics
Malignancy?
SLE
Presentation
Prodrome
of
myalgias
, fevers, cough, sore throat
Lesions begin around face and trunk with some extremity involvement
Erythematous
macules
and papules that start to have skin sloughing
Nikolsky
sign
Stomatitis
(erosive)
Conjunctivitis
Esophagitis
Respiratory Failure
Slide38Slide39Primarily due to electrolyte abnormalities and infectionVision lossVaginal stenosis Organ failure secondary to septic shockSCORTEN
Morbidity and Mortality
180 mg/dl
2
50 mg/dl
Slide40IDENTIFICATIONPROPER DISPOSITION: SCORTEN greater or equal to 2 should go to burn unitStop the suspected drugSteroidsNo consensusIVIG, plasmapheresis, Anti-TNF, cyclosporineSmall studies, not recommended
Management
Slide41EM MinorEM MajorSJSTENEpidermal detachmentNoNoYesYesMucosal InvolvementNoYesYesYesMost Common etiologyInfectiousInfectiousDrugDrugDegree of epidermal detachment %BSA00<10%>30%
Comparing Drug Reactions
Slide42IgG against keratinocytesPresentationElderly with oral erosions, vesicles and bullae for weeks to monthsThen get skin vesicles and bullaeSlow progressive disease
Pemphigus Vulgaris
Slide43Treat with steroids (1 mg/kg/day)Admit if signs of infection or toxicityOutpatient Dermatology follow up
Management
Slide44Slide45Neisseria meningitidis infection that includes bacteremia with CNSRisk factorsCrowded environmentsComplement deficienciesAsplenic patientsProtein C and S deficienciesUsually occur in ages 6 months to 1 year and young adults (usually less than 20)
Meningococcemia
Slide46Often first appears to be viral URIGet petechiae starting at wrist and ankles that spread and become papulesMeningitis symptomsQuickly become septic: multiorgan failure and DICCan get hemorrhagic destruction of adrenal glands (Waterhouse-Friderichsen syndrome)
Slide47Get blood cultures and punch biopsy (significantly more sensitive than CSF gram stain)
Treat with
ceftriaxone
2 g q12
If still concerned for Rocky mountain spotted fever add
doxycycline
For severe penicillin allergies use IV
chloramphenicol
4g per day
Close contacts (day care personnel, people sharing housing, ED who are in contact with oral secretions or someone who has been in contact for 4 hours over the past week get prophylaxis
Cipro
500 mg once
Rifampin
600 mg BID for two days
Single dose IM
ceftriaxone
250 mg (pregnancy)
Slide48Immune mediated destruction of plateletsUsually idiopathicSecondary causesHIV, HCVSLECLLPetechia and purpura usually in dependent areasSignificant bleed in approximately 10%: Usually GI rarely ICHCBC and coags show isolated thrombocytopenia
Immune Thrombocytopenic Purpura
Slide49ICH or GI bleed and plt<30,000PlateletsIVIG (1g/kg)Steroids(methylprednisone 1 g/d for 3 days)Bleeding or new diagnosis and plt <30,000Steroids (methylprednisone 1g/d for 3 days)IVIG (1g/kg) only if bleedingPlt 20,000 to 30,000 with no bleeding: observationPediatricsOnly treat if significant bleedingMost cases self resolve in less than 3 months
Slide50Microangiopathic hemolytic anemia
Thrombotic Thrombocytopenic Purpura
Slide51Microangiopathic Hemolytic Anemia (SOB, fatigue, chest pain)Thrombocytopenia (bleeding)FeverRenal insufficiencyNeurologic finding (headache, confusion, dizziness, stroke, coma)
TTP Pentad
Slide52AnemiaThrombocytopeniaEvidence of hemolyticSchistocytesElevated LDH and billirubinADAMTS13 assay
Labs
Slide53AdmitPlasma exchangeNeeds to be started earlyIf high clinical suspicion get started before all labs are backGet hematology involved earlySteroids: 125 mg methylprednisone IV Q6-12
Management
Slide54Slide55Staph aureusLocal infection causing shock due to toxinsEnterotoxin and toxic shock syndrome toxinToxins are super antigens that directly activate T cells at MHC without the need for antigen presenting cellsGroup A StrepLocal infection post surgical or after traumaVery painful and tender area of infectionBacteremia leads to sepsis
Staphylococcal and
Streptoccocal
Toxic Shock Syndrome
Slide56Slide57Like any other infectionFind your sourceSource controlAntibiotics (clindamycin and vancomycin/zosyn/carbapenem)Fluid resuscitationIonotropic support if needed
Management
Slide58Questions