DERMATOLOGY AND RHEUMATOLOGY
DERMATOLOGY AND RHEUMATOLOGY
B
Y DR OLALEKAN ADISA
DERMATOLOGY AND RHEUMATOLOGY
•
STAPHYLOCOCCAL SCALDED SKIN SYNDROME
•
ERYTHEMA MULTIFORME
•
S
TEVEN JOHNSON SYNDROME
•
T
OXIC EPIDERMAL NECROLYSIS
•
S
YSTEMIC LUPUS ERYTHEMATOSUS
S
KIN LAYERS
S
TAPHYLOCCOCAL SCALDED SKIN SYNDROME
•
Staphylococcal scalded skin syndrome(SSSS): is an illness characterised by red blistering skin that
looks like burns or scald.
•
SSSS is caused by exfoliative epidermolysis exotoxin of Staphyloccus aureus.
•
Desmosomes are attacked and destroyed by toxins
•
Blister formation and rupture in24-48hours
S
TAPHYLOCCOCAL SCALDED SKIN SYNDROME
•
Formation of burn-like skin area
•
Start around the flexure area of the body
•
Common in infant and <5years
•
Neonates, Immunocompromised individuals, individual with renal failure and Elderly are at risk
R
ISK FACTORS
1) Low immunity
•
Infants
•
Elderly
•
Immunocompromised individuals
2) Individual with renal failure
DIAGNOSIS
•
HISTORY:
Rash, irritable,fever etc
•
E
XAMINATION:
Peeling skin, Nicolsky sign +ve
•
I
NVESTIGATIONS: FBC,
Serum chemistry, skin,urine & blood culture, skin biopsy
TREATMENT
•
ABC APPROACH
•
SUPPORTIVE
•
A
NTIBIOTICS
COMPLICATIONS
•
SEVERE D
EHYDRATION
•
P
NEUMONIA
•
S
EPSIS
•
SEVERE INFECTION: S
HOCK
PROGNOSIS
E
RYTHEMA MULTIFORME
•
D
IFINITION
•
T
YPES
•
E
PIDEMIOLOGY
•
C
AUSES
•
C
LINICAL FEATURES
•
T
REATMENTS
•
COMPLICATIONS
ERYTHEMA MULTIFORME
•
Erythema multiforme is an immune-mediated mucocutaneous condition characterised by “target”
lesions.
•
It is a skin reaction that can be triggered by an infection or some medicines.
TYPES
2 Types: Minor and Major
•
Minor: It's usually mild and goes away in a few weeks.
•
Major: a rare, severe form that can affect the mouth, genitals and eyes and can be life-
threatening.
EPIDERMIOLOGY
•
Erythema multiforme mainly affects children and young adults(adults under 40)
•
Although it can happen at any age.
•
Slightly affects more males than females
•
In UK: Incidence is unknown, but account for 1% of clinician visit of dermatological problems
•
Globally: 1.2-6 cases per million individuals per year
CAUSES
•
Idiopathic
•
Infections
•
Drugs
CAUSES
Some medicines can occasionally cause the more severe form of erythema multiforme. Possible
medicine triggers include:
•
Antibiotics such as sulfonamides, tetracyclines, amoxicillin and ampicillin
•
NSAIDs such as Ibuprofen
•
Anticonvulsants such as phenytoin and barbiturates
CAUSES
Infections: Viral, bacterial
•
Most cases are caused by a viral infection – often the herpes simplex (cold sore) virus. This virus
usually lies inactive in the body, but it can become reactivated from time to time.
•
Some people will get a cold sore a few days before the rash starts.
•
Erythema multiforme can also be triggered by mycoplasma bacteria, a type of bacteria that
sometimes cause chest infections.
C
LINICAL FEATURES
•
The rash starts suddenly and develops over a few days.
•
It tends to start on the hands or feet
•
Later spreading to the limbs, upper body and face.
•
It is usually self limiting and resolves within 2-4weeks in most cases.
CLINICAL FEATURES
The rash:
•
Starts as small red spots, which may become raised patches a few centimetres in size
•
Often has patches that look like a target or "bulls-eye", with a dark red centre that may have a blister or crust,
surrounded by a pale pink ring and a darker outermost ring
•
May be slightly itchy or uncomfortable
•
Usually fades over 2 to 4 weeks
•
In more severe cases, the patches may join together to form large, red areas that may be raw and painful.
CLINICAL FEATURES
Additional symptoms of erythema multiforme can include:
•
A high temperature
•
A headache
•
Feeling generally unwell
•
Raw sores inside your mouth, making it hard to eat and drink
OTHER CLINICAL FAETURES
•
Swollen lips covered in crusts
•
Sores on the genitals, making it painful to pee
•
Sore, red eyes
•
Sensitivity to light and blurred vision
•
Aching joints
DIAGNOSIS
•
H
ISTORY
•
E
XAMINATION
•
INVESTIGATION
TREATMENTS
Treatment aims:
•
To tackle the underlying cause of the condition
•
Relieve your symptoms
•
And stop your skin becoming infected.
TREATMENTS
•
Stopping any medicine that may be triggering your symptoms
•
Antihistamine and moisturising cream, emollients, to reduce itching
•
Steriod cream to reduce redness and swelling (inflammation)
•
Painkillers for any pain
•
Antiviral tablets, if the cause is a viral infection
•
Anaesthetic mouthwash to ease the discomfort of any mouth sores
TREATMENTS
Severe cases:
•
Stronger painkillers
•
Wound dressings to stop the sores becoming infected
•
A softened or liquid diet if mouth is badly affected – some people may need fluids given through a
drip into a vein
•
Steriod tablets to control the inflammation
•
Antibiotics if there is a bacterial infection
•
Eye drops or ointment if eyes are affected
COMPLICATIONS
•
Most people with erythema multiforme make a full recovery within a few weeks. There are usually
no further problem and the skin heals without scarring.
•
There is a risk the condition could come back at some point, especially if it was caused by
the herpes simplex virus.
•
You may be given antiviral medicine to prevent attacks if you experience them frequently.
COMPLICATIONS
In severe cases, possible complications can include:
•
A skin infection (cellulitis)
•
Sepsis
•
Permanent skin damage and scarring
•
Permanent eye damage
•
Inflammation of internal organs, such as the lungs
EM/SJS/TEN
SJS/TEN
S
TEVENS-JOHNSON SYNDROME
•
D
EFINITION
•
T
YPES/VARIANTS
•
E
PIDEMIOLOGY
•
C
LINICAL FEATURES
•
C
AUSES
•
T
REATMENT
•
COMPLICATIONS
STEVENS-JOHNSON SYNDROME
Stevens-johnson syndrome (SJS) is a serious disorder of the skin and mucous membrane.
•
It is usually a reaction to medication.
•
It starts with aflu-like symtoms
•
A
nd followed by a painful rash
•
Rash spreads and blisters
•
Then the top layer of the affected skin dies, sheds and begins to heal after several days.
•
STEVENS – JOHNSON SYNDROME (SJS)
•
T
OXIC EPIDERMAL NECROLYSIS(TEN)
•
S
JS/TEN OVERLAP
EPIDERMIOLOGY
SJS/TEN
:
•
Rare
•
0.4-1.3 per million individual
•
F
emale >Male
•
Children and young adults/older adults
CAUSES
SJS is a rare and unpreditable illness
and cause may or may not be be identified.
•
Medication(up to 2 weeks)
•
Infection
•
Both
CAUSES
Medications:
•
Allopurinol(especially >100mg/day)
•
Anticonvulsants & antipsychotics
•
Antibacterial/sulfonamides
•
Nevirapine(viramune, viramune XR)
•
Pain relievers(acetamenophen, NSAIDS)
CAUSES
M
edications:
•
Anticonvulsants: Lamotrgine, carbamazipine, phenytoin, phenobarbitone
•
Sulfonamides: cotrimoxazole, sulfasalazine
CAUSES
INFECTIONS:
•
BACTERIAL INFECTION
: Pneumonia caused by mycoplasma pneumoniae
•
VIRAL INFECTION:
Herpes simplex
R
ISK FACTORS
•
H
IV infection: 100 times >general population
•
A weakned immune system: organ transplant, HIV/AIDS & autoimmune diseases
•
Cancer: particularly blood cancer are at increased risk of SJS
•
Past hx of SJS
•
A family Hx of SJS in im
m
ediate blood relative
•
Genetic factors: certain genetic variation called HLA-B*1502 in Asian & south Asian ancestry,
especially if also taking drugs for seizure, gout or mental illness.
C
LINICAL FEATURES
Early(1-3 days):
•
Fever
•
A sore mouth and throat
•
Fatigue
•
Burning eyes
C
LINICAL FAETURES
Later(as the condition develops):
•
Unexplained widespread skin pain
•
A red or purple rash that spreads
•
Blisters on the skin and mucous membranes of the mouth, nose, eyes and genitals
•
Shedding of the skin withins days after blisters form
DIAGNOSIS
•
History
•
Physical examination
•
Investigations: to confirm and or rule out other causes(Blood tests, imaging-CXR-pneumonia, culture-
to rule infection, and skin biopsy-to confirm and rule out other possible causes
TREATMENT
SJS is an emergency and might requires ICU/burn unit.
•
Stop all medications especially the non essential drugs
•
Supportive care(ABC)
TREATMENT
S
upportive care:
•
F
luid replacement and nutrition(NG tube feeding)
•
W
ound care: cool, wet compression, blister/dead tissue removal, petrolleum jelly, and wound
dresssing
•
MDT- urologist(stricture)
•
Eye care: may need ophthalmologist
TREATMENT
•
Pain medication: to reduce discomfort
•
M
edication(topical steriods) to reduce inflamation of eyes/mucous membranes
•
A
ntibiotics: to control infection, when needed.
•
Respiratory support:oxygen, suctioning, nebulisation, endotracheal intubation
•
O
ther oral and systemic drugs: corticosteriods, IV immune globulins, immunosupressant(
C
yclosporin),
TNF alpha inhibitor(etanercept)
COMPLICATIONS
•
Dehydration
•
Sepsis: infection, shock & organ failure.
•
Eye problem: inflamation,dry eye, photo sensitivity, visual impairment, blindness(severe cases)
•
Lung involvement: acute respiratory failure
•
Permanent skin damage: dyspigmentation, scars, hair loss etc.
T
OXIC EPIDERMAL NECROLYSIS
•
SJS affects <10% of the body, children and younger adults.
•
Toxic epidermal necrolysis(TEN) causes peeling skin affecting > 30% of the body
•
TEN affects all age groups but more likely older adults.
•
TEN medication ceasation of hx of up to 8weeks prior to symtoms onset
•
TEN is a medical emergency and reqiures ICU/burns unit admission
PROGNOSIS
Severity of illness scale called SCORTEN scale: it uses 7 independent as risk factors are
systematically scored to to prognasticate morbility and mortality
S
CORTEN SCALE
PROGNOSIS
T
AKE HOME
•
SJS may begin like the flu, with lesions appearing 1-3 days after the prodrome starts
•
Have to have a high suspicion for SJS because it is deadly. It’s a clinical diagnosis — derm biopsy is supportive
•
A thorough history and physical exam are key.
•
Remember the characteristic rash and bullae, and always look in the mouth and eyes. Ask about dysuria, sore
throat, and eye irritation, as well as preceding medications or infections.
•
Think SATAN!
•
Prompt supportive care focused on ABCs and ivf repletion are critical.
•
These patients can get sick really fast, so consider an ICU or burn unit.
S
YSTEMIC LUPUS ERYTHEMATOSUS
S
YSTEMIC LUPUS ERYTHEMATOSUS(SLE):
Is a chronic, autoimmune disease and it usually affects
different organs of the body:
•
skin and mucous membrane
•
L
ungs
•
H
eart
•
K
idneys
•
B
lood and blood vessels
•
J
oints
•
Brain and N
ervous system
EPIDEMIOLOGY
•
O
ne of the comonest autoimmune diseases
•
A
ffect over 5 million Americans each year
•
UK: 20 per 100,000 of the population
•
F
emale>male
•
M
ore common in African and Asian women
T
YPES/VARIANTS
•
M
ILD:
Joint and skin, tiredness
•
M
oderate: inflamation of the otherpart of the skin and body, lungs, heart and kidneys.
•
S
evere: inflamation causing cevere damage to the heart, lungs, brain or kidneys and can be life
threatening.
CAUSES
Exact cause of SLE is u
nknown but asscoiated factors include:
Genetics: people with family hx of autoimmune conditions
Enviromental triggers:
•
Sunlight
•
C
ertain medicines
•
viruses
•
P
hysical and emotional stress
Sex and hormones:(F>M,puberty,pregnancy and menopause)/oestrogen)
M
ULTIORGAN AFFECTATION
•
Skin and mucus membranes: malar rash,hairloss, nose and mouth ulcer
•
Heart: endocarditis,pericarditis,valvular problems, atheriosclerosis,hypertension/heart failure
•
Lungs: pleuritis,pneumonitis,PE, pulmonary haemorrhage
•
Blood/blood vessels: severe anaemia/Thrombotic thrombocytopenia purpura(TTP)/nuetropenic
sepsis
M
ULTIORGAN AFFECTATION
•
Muscle and joits: arthritis/muscle pain/weakness
•
Kidneys: lupus nepritis
•
GIT: severe abdominal pain/Gatritis/pseudo-intestinal obstuction,SBP
•
Nervous tissues: perpheral neuropathy, stroke, headache, seizures, cognitive propblem(learning
disability), anxiety, depression
CLINICAL FEATURES
•
Sun sensitive rash: malar or butterfly rash
•
Hair thinning/hair loss
•
Nose or mouth ulcers
•
Muscle pain and Small joints of hands/feet/wrist swelling and tenderness
•
Irregular heart beats, murmur and rubs
C
LINICAL FEATURES
•
Pleuritic chest dicomfort/pain
•
Fatigue
•
A
bdomal pain
•
Headache
•
Fever
INVESTIGATIONS
Blood tests: antibody(ANCA), FBC, Renal panel etc.
Urine test
Biopsy
Radiologic
ED DIAGNOSTICS
E
D DIAGNOSTICS
C
LASSIFICATION CRITERIA FOR SLE
C
LINICAL CRITERIA
•
Acute Cutaneous Lupus
•
Chronic Cutaneous Lupus
•
Oral or Nasal Ulcers
•
Non-scarring alopecia
•
Arthritis
•
S
erositis
•
Renal
•
Neurologic
•
Hemolytic anaemia
•
Leucopenia
•
Thrombocytopenia
I
MMUNOLOGIC CRITERIA
•
ANA
•
Anti-DNA
•
Anti-Smith
•
A
ntiphospholipid Ab
•
L
ow complement(C3,C4,CH50)
•
Direct Coombs Test(outside of the presence of
hemolytic anaemia)
CRITERIA FOR SLE
Required 4 criteria:
•
At least 1 clinical and 1 laboratory criteria OR
•
Bioopsy-proven lupus nephritis with positive ANA or Anti-DNA
DIAGNOSIS
C
riteria: 4 of the 11
•
A butterfly-shaped rash across both sides of the face.
•
Raised, red skin patches
•
Sensitivity to light
•
Ulcers in the mouth or nose
•
Arthritis plus swelling or tenderness in two or more joints
DIAGNOSIS
•
Seizures or other nervous system problems
•
Excessive protein in urine
•
Inflammation in the lining of the heart or lungs
•
Low blood cell counts
•
The presence of certain antibodies in the blood
•
ANA test results indicating the presence of too many antinuclear antibodies
TREATMENT
S
LE is a chronic disease
It has no cure.
Flare ups can be managed
The goal of treatment is to ease symtoms and manage complications
Treatment options depend on the the body part/organ that is affected by SLE
TREATMENTS
•
Anti inflamatory drugs: for joint pains/stiffness
•
C
orticosteriods: to minimise immune response
•
S
teriod creams: rashes
•
Diet & lifestyle habits to reduce physical and emotional stress
•
Disease modifying drugs or Target immune system agents in severe cases
COMPLICATIONS
•
Vasculitis
•
P
ericarditis/heart attacks
•
Pleuritis
•
Stroke/seizures/memory & behavioural changes
•
K
idney inlamation/decreased kidney function/ kidney failure
COMPLICATIONS
GIT:
•
Gastritis
•
Lupus enteritis
•
Pseudo-intestinal obstruction
•
Spontaneous bacteria peritonitis
COMPLICATIONS
C
A
RDIOVASCULAR:
•
ACS
•
Pericarditis, myocardiris,endocarditis
•
C
ardiac tamponade
•
Heart failure
COMPLICATIONS
PULMONARY
•
Pleurisy
•
Acute lupus pneumonitis
•
Acute pulmonary hemorrhage
•
Pulmonary embolism
COMPLICATIONS
RENAL
•
Acute lupus nephritis
•
AKI/ Acute kidney failure
•
NEUROLOGIC:
•
Stroke
•
Depression/mania
•
Psychosis
•
Coma
PREGNANCY
•
Gestational DM
•
PIH, Pre-eclampsia/eclampsia
•
Premature rupture of membrane
•
Thromboembolic events
CONCLUSION
TAKE HOME ON:
•
SSSS
•
EM/SJS/TEN
•
SLE
REFERENCES
THANK YOU
Staphylococcal Scalded Skin Syndrome (SSSS) is a serious condition characterized by red blistering skin resembling burns. It is caused by toxins from Staphylococcus aureus, leading to exfoliation of the skin. Common in infants, the elderly, and immunocompromised individuals, SSSS requires prompt diagnosis through history, examination, and investigations like skin biopsies. Treatment involves a supportive approach and antibiotics, while complications can include severe dehydration, pneumonia, sepsis, and shock.
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DERMATOLOGY AND RHEUMATOLOGY BY DR OLALEKAN ADISA
DERMATOLOGY AND RHEUMATOLOGY STAPHYLOCOCCAL SCALDED SKIN SYNDROME ERYTHEMA MULTIFORME STEVEN JOHNSON SYNDROME TOXIC EPIDERMAL NECROLYSIS SYSTEMIC LUPUS ERYTHEMATOSUS
STAPHYLOCCOCAL SCALDED SKIN SYNDROME Staphylococcal scalded skin syndrome(SSSS): is an illness characterised by red blistering skin that looks like burns or scald. SSSS is caused by exfoliative epidermolysis exotoxin of Staphyloccus aureus. Desmosomes are attacked and destroyed by toxins Blister formation and rupture in24-48hours
STAPHYLOCCOCAL SCALDED SKIN SYNDROME Formation of burn-like skin area Start around the flexure area of the body Common in infant and <5years Neonates, Immunocompromised individuals, individual with renal failure and Elderly are at risk
RISK FACTORS 1) Low immunity Infants Elderly Immunocompromised individuals 2) Individual with renal failure
DIAGNOSIS HISTORY: Rash, irritable,fever etc EXAMINATION: Peeling skin, Nicolsky sign +ve INVESTIGATIONS: FBC, Serum chemistry, skin,urine & blood culture, skin biopsy
TREATMENT ABC APPROACH SUPPORTIVE ANTIBIOTICS
COMPLICATIONS SEVERE DEHYDRATION PNEUMONIA SEPSIS SEVERE INFECTION: SHOCK
ERYTHEMA MULTIFORME DIFINITION TYPES EPIDEMIOLOGY CAUSES CLINICAL FEATURES TREATMENTS COMPLICATIONS
ERYTHEMA MULTIFORME Erythema multiforme is an immune-mediated mucocutaneous condition characterised by target lesions. It is a skin reaction that can be triggered by an infection or some medicines.
TYPES 2 Types: Minor and Major Minor: It's usually mild and goes away in a few weeks. Major: a rare, severe form that can affect the mouth, genitals and eyes and can be life- threatening.
EPIDERMIOLOGY Erythema multiforme mainly affects children and young adults(adults under 40) Although it can happen at any age. Slightly affects more males than females In UK: Incidence is unknown, but account for 1% of clinician visit of dermatological problems Globally: 1.2-6 cases per million individuals per year
CAUSES Idiopathic Infections Drugs
CAUSES Some medicines can occasionally cause the more severe form of erythema multiforme. Possible medicine triggers include: Antibiotics such as sulfonamides, tetracyclines, amoxicillin and ampicillin NSAIDs such as Ibuprofen Anticonvulsants such as phenytoin and barbiturates
CAUSES Infections: Viral, bacterial Most cases are caused by a viral infection often the herpes simplex (cold sore) virus. This virus usually lies inactive in the body, but it can become reactivated from time to time. Some people will get a cold sore a few days before the rash starts. Erythema multiforme can also be triggered by mycoplasma bacteria, a type of bacteria that sometimes cause chest infections.
CLINICAL FEATURES The rash starts suddenly and develops over a few days. It tends to start on the hands or feet Later spreading to the limbs, upper body and face. It is usually self limiting and resolves within 2-4weeks in most cases.
CLINICAL FEATURES The rash: Starts as small red spots, which may become raised patches a few centimetres in size Often has patches that look like a target or "bulls-eye", with a dark red centre that may have a blister or crust, surrounded by a pale pink ring and a darker outermost ring May be slightly itchy or uncomfortable Usually fades over 2 to 4 weeks In more severe cases, the patches may join together to form large, red areas that may be raw and painful.
CLINICAL FEATURES Additional symptoms of erythema multiforme can include: A high temperature A headache Feeling generally unwell Raw sores inside your mouth, making it hard to eat and drink
OTHER CLINICAL FAETURES Swollen lips covered in crusts Sores on the genitals, making it painful to pee Sore, red eyes Sensitivity to light and blurred vision Aching joints
DIAGNOSIS HISTORY EXAMINATION INVESTIGATION
TREATMENTS Treatment aims: To tackle the underlying cause of the condition Relieve your symptoms And stop your skin becoming infected.
TREATMENTS Stopping any medicine that may be triggering your symptoms Antihistamine and moisturising cream, emollients, to reduce itching Steriod cream to reduce redness and swelling (inflammation) Painkillers for any pain Antiviral tablets, if the cause is a viral infection Anaesthetic mouthwash to ease the discomfort of any mouth sores
TREATMENTS Severe cases: Stronger painkillers Wound dressings to stop the sores becoming infected A softened or liquid diet if mouth is badly affected some people may need fluids given through a drip into a vein Steriod tablets to control the inflammation Antibiotics if there is a bacterial infection Eye drops or ointment if eyes are affected
COMPLICATIONS Most people with erythema multiforme make a full recovery within a few weeks. There are usually no further problem and the skin heals without scarring. There is a risk the condition could come back at some point, especially if it was caused by the herpes simplex virus. You may be given antiviral medicine to prevent attacks if you experience them frequently.
COMPLICATIONS In severe cases, possible complications can include: A skin infection (cellulitis) Sepsis Permanent skin damage and scarring Permanent eye damage Inflammation of internal organs, such as the lungs
STEVENS-JOHNSON SYNDROME DEFINITION TYPES/VARIANTS EPIDEMIOLOGY CLINICAL FEATURES CAUSES TREATMENT COMPLICATIONS
STEVENS-JOHNSON SYNDROME Stevens-johnson syndrome (SJS) is a serious disorder of the skin and mucous membrane. It is usually a reaction to medication. It starts with aflu-like symtoms And followed by a painful rash Rash spreads and blisters Then the top layer of the affected skin dies, sheds and begins to heal after several days.
STEVENS JOHNSON SYNDROME (SJS) TOXIC EPIDERMAL NECROLYSIS(TEN) SJS/TEN OVERLAP
EPIDERMIOLOGY SJS/TEN: Rare 0.4-1.3 per million individual Female >Male Children and young adults/older adults
CAUSES SJS is a rare and unpreditable illness and cause may or may not be be identified. Medication(up to 2 weeks) Infection Both
CAUSES Medications: Allopurinol(especially >100mg/day) Anticonvulsants & antipsychotics Antibacterial/sulfonamides Nevirapine(viramune, viramune XR) Pain relievers(acetamenophen, NSAIDS)
CAUSES Medications: Anticonvulsants: Lamotrgine, carbamazipine, phenytoin, phenobarbitone Sulfonamides: cotrimoxazole, sulfasalazine
CAUSES INFECTIONS: BACTERIAL INFECTION: Pneumonia caused by mycoplasma pneumoniae VIRAL INFECTION: Herpes simplex
RISK FACTORS HIV infection: 100 times >general population A weakned immune system: organ transplant, HIV/AIDS & autoimmune diseases Cancer: particularly blood cancer are at increased risk of SJS Past hx of SJS A family Hx of SJS in immediate blood relative Genetic factors: certain genetic variation called HLA-B*1502 in Asian & south Asian ancestry, especially if also taking drugs for seizure, gout or mental illness.
CLINICAL FEATURES Early(1-3 days): Fever A sore mouth and throat Fatigue Burning eyes
CLINICAL FAETURES Later(as the condition develops): Unexplained widespread skin pain A red or purple rash that spreads Blisters on the skin and mucous membranes of the mouth, nose, eyes and genitals Shedding of the skin withins days after blisters form
DIAGNOSIS History Physical examination Investigations: to confirm and or rule out other causes(Blood tests, imaging-CXR-pneumonia, culture- to rule infection, and skin biopsy-to confirm and rule out other possible causes
TREATMENT SJS is an emergency and might requires ICU/burn unit. Stop all medications especially the non essential drugs Supportive care(ABC)
TREATMENT Supportive care: Fluid replacement and nutrition(NG tube feeding) Wound care: cool, wet compression, blister/dead tissue removal, petrolleum jelly, and wound dresssing MDT- urologist(stricture) Eye care: may need ophthalmologist
