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in allergic disease
Prof. DR. dr. Endang Sutedja, SpKK (K)
Case Report
1 week : 3 days:
Cough GP Generalized
(Community Health Center) erythematous
macules & papules
Medication : Itchy (+), fever (+)
- White tablet 3x/day
- White caplet 3x/day
2 days : 1 day : HOSPITAL
General :
Stop suspected medications
Consult to Dept.Internal Medicine,
Ophthalmology and ENT
Specific :
Topical
Systemic
Ringer Lactate infusion
Prednisone 3 mg/kg BW/day short term
(3 – 0 - 1.5) ampule dexamethasone inj
5th day :
ICU
DEATH
Her husband and family :
Did not accept it
Want to sue the GP and doctor in
hospital
1.During the patient was critically ill
2.Treatment and procedure in hospital
3. If you were the GP who
gave those suspected
medications for the first time
Expectation/answer
Humoral Cellular
ALLERGY ALLOS + ERGOS
Hypersensitivy reactions
Prophylaxis
Treatment
Port of entry :
- Gastro-intestinal tract
- Respiratory tract
- IV;ID;IM
- Topical
Drug reaction all reaction in the body induced by
drugs
- toxicity
- overdosis
- intolerance
- allergy, etc.
Diagnosis :
1. Accurate anamnesis :
Given medication
Acute onset a few hours
Itching/sub-febrile
2. Cutaneous abnormalities :
Distribution : diffuse & symmetry
Single drug-induced abnormalities,
Multiple drug-induced abnormalities similar
disorders
FORMS :
Urticaria
Erythema morbilliform
Dermatitis
Purpura
Exanthema fixtum (Fixed Drug Eruption)
- Hyperpigmentation :
permanent/transient
- Relaps
- Similar sites
Predilection labia (lips); penis
Erythema nodosum
Erythroderma
FIXED DRUG ERUPTIONS
Clinical manifestations :
- erytemathous dan vesikel/bula
hyperpigmentation macule (menetap)
- Many times appear in the same place
- predilections : round the mouth, >> lip
in a man : penis
STEVENS-JOHNSON’S
Definition : SYNDROME
Syndromes Skin
Orificial and ocular mucosa
Varied general state: mild ---
severe
Synonym : erythema multiforme mayor
Etiology :
Systemic drug-induced allergy
Infection
Neoplasm
Pathogenesis :
type I-IV
DIAGNOSIS :
Mild severe decreased consciousness soporous
coma
TRIAD :
-Skin disorder
-Orificial mucous disorder
-Opthalmic disorder
Complication :
• Bronchopneumonia
• Loss of body fluid shock
• Eye blindness, lacrimation
THERAPY :
-Care,General state, Infuse
-Corticosteroid life saving
-4-6 x 5 mg/day critical period (3days)
-Get decreased to be 5mg/day per day 1x5 mg
-Antibiotics (carefully)
PROGNOSIS :
Take action immediately,and appropriately good prognosis
Death 5 – 15 %
TEN
More severe than Steven-Johnson’s syndrome
Epidermolysis
Mucosa
Synonym : Lyell’s syndrome
Etiology : similar with Steven-Johnson’s
Syndromes : severe death
fluid–electrolyte imbalance
Prodromal :
Severe illness
High fever
Soporo comatous
Skin : erythema generalisata vesicle bulla purpura
With the mucosa of :
Oral/lips
Erosion/excoriation
Crust
Patological anatomy : Epidermolysis
Nikolsky sign (+)
Therapy : similar to Steven-Johnson syndrome
Prognosis :
5 – 7% worse
Infection is better than drugs
Death 28.6%
Steven-Johnson syndrome 1 %
Dermatological Status
Laboratory
Hb : 13,8 g/dl
Leukocyte : 10.800 g/dl
Thrombocyte : 325.000 g/dl
Gravity index : 1,024
Liver and kidney function test : normal
Electrolyte : normal
Chest X-ray : laryngeal obstruction (-)
Case
There was a young boy, 10 yr old with
Steven Johnson Syndrome (SJS)
Anamnesis: 4 days ago fever
hours
• Syr. Antibiotic
• Analgetic Death