It is 100 times more common in association with human immunodeficiency virus infection (HIV). Before Stevens-Johnson syndrome and abuse of anabolic steroids. [1] Typical onset is under the age of 30. Symptoms can include: Painful blistering of the skin and mucous membrane involvement. Consider genetic testing before taking certain drugs. Rev Assoc Med Bras (1992). blisters; dental emergency; oral mucosal lesions; oral ulcers; skin rash; stevens-johnson syndrome (sjs). 2020;12:0. Among people who survive, long-term effects of Stevens-Johnson syndrome/toxic epidermal necrolysis can include changes in skin coloring (pigmentation), dryness of the skin and mucous membranes (xerosis), excess sweating (hyperhidrosis), hair loss (alopecia), and abnormal growth or loss of the fingernails and toenails. Plasmapheresis can remove reactive drug metabolites or antibodies and can be considered. What are the clinical symptoms of these three levels of patients and how to treat them? People with systemic lupus erythematosus or HIV infections are more susceptible to drug-induced SJS. Stevens-Johnson syndrome/toxic epidermal necrolysis often begins with a fever and flu-like symptoms. Stevens-Johnson syndrome /toxic epidermal necrolysis (SJS/TEN) The overall mortality rate is about 25%, ranging from about 10% for SJS to over 30% for TEN. The most common causes of death include sepsis, acute respiratory distress syndrome, and multiple organ failure. Those that survive may experience recurrence (particularly if re-exposed Treatment of Steven-johnson syndrome is most successful when Stevens-Johnson syndrome and toxic epidermal necrolysis are recognized early and treated in an inpatient dermatologic or intensive care unit setting; treatment in a burn unit may be needed for severe disease. Before the rash appears, there is usually a prodromal illness of several days duration resembling an upper respiratory tract infection or flu-like illness. StevensJohnson syndrome Bullous erythema multiforme, Figure 5. Seborrheic dermatitis is common in people with HIV, most often occurring in the early stages of HIV, when blood counts of CD4 (white blood cells that are important to fighting infections) are at around 400. Erythema multiforme major is also known as Stevens-Johnson syndrome. The role of systemic corticosteroids (cortisone) remains controversial. The use of systemic corticosteroids remains controversial. [36], Variations in ADME, i.e. Variation of a specific gene called human leukocyte antigen-B. In the United States, about 300 new diagnoses are made each year. [7][4] These ADME abnormalities, it is also suggested, may interact with particular HLA proteins and T cell receptors to promote a SCARs disorder. WebThe syndrome varies widely in severity and can range from mild symptoms such as hypertension to severe symptoms such as agitation, hallucinations, fever, vomiting, and spastic muscle contractions. Some changes in kidney function occur in the majority. Bookshelf Differential diagnosis of StevensJohnson syndrome / toxic epidermal necrolysis. During the acute phase, potentially fatal complications include: StevensJohnson syndrome / toxic epidermal necrolysis is a rare and unpredictable reaction to medication. Rinse with the hand shower, lifting the nursing board above the bath. Presoak the stick with the mouthwash solution. Mucosal involvement is prominent and severe, although not forming actual blisters. Flumiolone is anti-inflammatory. It doesn't matter. Early diagnosis and management play an important role in stopping SJS from progression. National Library of Medicine }); Who gets Stevens-Johnson syndrome/toxic epidermal necrolysis? Keywords: FDA Safety Alert: Infants at Risk for Aluminum Toxicity with This Unapproved Drug Product, U.S. Supreme Court Overturns Doctors Opioid Prescription Conviction. Stevens-Johnson syndrome and toxic epidermal necrolysis: a review. One point is scored for each of seven criteria present at the time of admission. Although SJS can be caused by viral infections and malignancies, the main cause is medications. Once the ocular surface is damaged to this extent, surgery is needed to restore the anatomical structure and physiological characteristics of the ocular surface, so as to rebuild the cornea and conjunctival epithelium. Those with chronic ocular surface disease caused by SJS may find some improvement with PROSE treatment (prosthetic replacement of the ocular surface ecosystem treatment). At this point, you may be confused. The category cannot always be defined with certainty on initial presentation. The various immunomodulatory treatments include systemic corticosteroids, cyclosporine, intravenous immunoglobulin, cyclophosphamide, Other HLA associations with the development of SJS, SJS/TEN, or TEN and the intake of specific drugs as determined in certain populations are given in HLA associations with SCARs. However, despite some remarkable initial results using high-dose IVIG for toxic epidermal necrolysis, further clinical trials involving small cohorts have reported conflicting results, and a retrospective analysis has suggested no improvement or even higher than expected mortality. Classification of Stevens-Johnson syndrome? CD8+ T cells) and T helper cells (i.e. Lerch M, Mainetti C, Terziroli Beretta-Piccoli B, Harr T. Clin Rev Allergy Immunol. Immediate withdrawal of all the suspected drugs is the key to the management of SJS-TEN. Maintenance of an ambient body temperature (31C32C), proper fluid-electrolyte balance, and maintenance of a strict aseptic environment are crucial. Banana leaf is used in many centers in India during the care of patients with SJS and TEN. More items The rash caused by Stevens-Johnson syndrome can lead to inflammation in your eyes. [13] These occur primarily on the torso. [1] Complications include dehydration, sepsis, pneumonia and multiple organ failure. [7][48], The diagnosis is based on involvement of less than 10% of the skin. The SCORTEN criteria are: The risk of dying from StevensJohnson syndrome / toxic epidermal necrolysis depends on the score. Clipboard, Search History, and several other advanced features are temporarily unavailable. Because its difficult to determine exactly which drug may be causing the problem, your doctor may recommend that you stop taking all nonessential medications. Mild proteinuria (protein leaking into urine) occurs in about 50%. [38][39][40] A study in Europe suggested the gene marker is only relevant for East Asians. (A) Blisters on the floor of the mouth; (B) buccal mucosa with scattered, Figure 4. Apply vitamin A or other sterile ocular lubricant ointment generously under the upper and the lower eyelid using one quarter of tube for one eye on each occasion. Signs of mucosal involvement can include the following: The following ocular signs may be noted on slit-lamp examination: Eyelids: Trichiasis, distichiasis, meibomian gland dysfunction, blepharitis, Conjunctiva: Papillae, follicles, keratinization, subepithelial fibrosis, conjunctival shrinkage, foreshortening of fornices, symblepharon, ankyloblepharon, Cornea: Superficial punctate keratitis, epithelial defect, stromal ulcer, neovascularization, keratinization, limbitis, conjunctivalization, stromal opacity, perforation (see the image below). HLA) serotypes, prosthetic replacement of the ocular surface ecosystem treatment, "Stevens-Johnson syndrome/toxic epidermal necrolysis", "Recent advances in the understanding of severe cutaneous adverse reactions", "Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Standard Reporting and Evaluation Guidelines", "StevensJohnson Syndrome: An intriguing diagnosis", "Profile and pattern of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in a general hospital in Singapore: Treatment outcomes", "The current understanding of StevensJohnson syndrome and toxic epidermal necrolysis", "ALDEN, an algorithm for assessment of drug causality in Stevens-Johnson Syndrome and toxic epidermal necrolysis: Comparison with case-control analysis", "Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)", "Clinical study of cutaneous drug eruptions in 200 patients", Indian Journal of Dermatology, Venereology and Leprology, "A case of bupropion-induced Stevens-Johnson syndrome with acute psoriatic exacerbation", "Carbamazepine The commonest cause of toxic epidermal necrolysis and StevensJohnson syndrome: A study of 7 years", "Acetaminophen induced Steven Johnson syndrome-Toxic Epidermal Necrolysis overlap", "Stevens-Johnson syndrome and toxic epidermal necrolysis", "Acute Generalized Exanthematous Pustulosis: Pathogenesis, Genetic Background, Clinical Variants and Therapy", "Classification of Drug Hypersensitivity into Allergic, p-i, and Pseudo-Allergic Forms", "HLA Association with Drug-Induced Adverse Reactions", "Medical genetics: A marker for StevensJohnson syndrome", "Association between HLA-B*1502 allele and antiepileptic drug-induced cutaneous reactions in Han Chinese", "A marker for StevensJohnson syndrome : Ethnicity matters", "A European study of HLA-B in StevensJohnson syndrome and toxic epidermal necrolysis related to five high-risk drugs", "Pharmacogenomics of off-target adverse drug reactions", "Reference SNP (refSNP) Cluster Report: rs1057910 ** With drug-response allele **", "Genetic variants associated with phenytoin-related severe cutaneous adverse reactions", "StevensJohnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN)", "Correlations between clinical patterns and causes of Erythema Multiforme Majus, Stevens-Johnson Syndrome, and Toxic Epidermal Necrolysis results of an international prospective study", "Is universal HLA-B*15:02 screening a cost-effective option in an ethnically diverse population? Anti-TNF monoclonal antibodies (eg, infliximab, etanercept), Intravenous immunoglobulin (IVIG) 23 g/kg given over 23 days. Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare, life-threatening mucocutaneous reactions most commonly triggered by medications, showing severe and extensive skin detachment.1 The overall mortality rate among patients with SJS/TEN is approximately 30%, ranging from 10% for SJS up to 50% for TEN. [29], Viral diseases reported to cause SJS include: herpes simplex virus (possibly; is debated), AIDS, coxsackievirus, influenza, hepatitis, and mumps. With decades of experience in medical and pharmaceutical lawsuits, our firm is dedicated to helping you win your SJS lawsuit and find peace, closure, and justice. White corneal scar in pupil area, with plenty of neovascularization. At the beginning, the skin was only a mild blister lesion, which further developed into toxic epidermal necrosis and dissolution. Case reports and small patient series have reported benefit from active adjuvant treatments delivered during the first 2448 hours of illness. Does Kisspeptin Shot Help With Low Libido? If the test result is positive, a blister will form in the area, usually within minutes. The patient or the health provider must put the petroleum-jelly-wrapped compress/glove into the vagina and gently remove it so that the jelly lubricates the lining of the vagina. No, Steven-johnson syndrome is not contagious, it is an unpredictable adverse reaction to certain medications. 1 Signs and symptoms. A. Abnormal eyelid position, entropion with trichiasis, C. Corneal limbal neovascularization grows in, but does not invade the pupil area, D. Conjunctival hyperemia, visible corded conjunctival scar, and the range of keratosis at the facial margin is greater than 1/3 and less than 1/2 of the entire palpebral margin. [33][34] Accordingly, only rare individuals are predisposed to develop a SCARs in response to a particular drug on the bases of their expression of HLA serotypes:[35] Studies have identified several HLA serotypes associated with development of SJS, SJS/TEN, or TEN in response to certain drugs. Law Office of Gretchen J. Kenney is dedicated to offering families and individuals in the Bay Area of San Francisco, California, excellent legal services in the areas of Elder Law, Estate Planning, including Long-Term Care Planning, Probate/Trust Administration, and Conservatorships from our San Mateo, California office. Other causes of StevensJohnson syndrome / toxic epidermal necrolysis. Dry eye is the most common complication in the chronic phase of SJS. [12] Malaria and trichomoniasis, protozoal infections, have also been reported as causes. Lasting skin problems may cause your hair to fall out, and your fingernails and toenails may not grow normally. Cyclosporine (3 to 5 mg/kg orally once/day) inhibits CD8 cells and has been shown to decrease the duration of active disease by 2 to 3 days in some instances and possibly decrease mortality. When the ocular surface damage of SJS patients is mild, there are few signs and mild symptoms. [50] Erythema multiforme, which is also within the SCAR spectrum, differs in clinical pattern and etiology. This condition affects 1 to 2 per million people each year. Stevens-Johnson syndrome signs and symptoms include: If you have Stevens-Johnson syndrome, several days before the rash develops you may experience: StevensJohnson syndrome / toxic epidermal necrolysis is suspected clinically and classified based on the skin surface area detached at maximum extent. If it was caused by a medication, youll need to permanently avoid that drug and others closely related to it. Artificial cornea implantation is the only choice for such patients. Your health care provider may use a pencil eraser to test for Nikolsky sign. People with a positive sign have loose skin that slips free from the underlying layers when rubbed. [13] The skin pattern most commonly associated with SJS is widespread, often joined or touching (confluent), papuric spots (macules) or flat small blisters or large blisters which may also join. We present a case of a 37-year-old male with no past medical history who presented to the dental emergency clinic complaining of dysphagia and burning sensation in the mouth. If your condition was caused by a medication, learn its name and that of closely related medications. Investigations in StevensJohnson syndrome / toxic epidermal necrolysis, Care of a patient with StevensJohnson syndrome / toxic epidermal necrolysis. The mortality for toxic epidermal necrolysis (TEN) is 3040%. Law Firm Website Design by Law Promo, What Clients Say About Working With Gretchen Kenney. Symptoms of drug-induced Steven Johnson syndrome appear about one to three weeks after you start taking medication. Please enable it to take advantage of the complete set of features! Why Is Dexamethasone Given Prior To Chemo? 2016;17:2135. Put some petroleum jelly on the eyelids if there is crust or erosions. More than 50% of the patients were complicated with ocular surface damage. Stevens The condition is more common in adults than in children. It had been thought by many experts to increase mortality because of increased rates of infection and the risk of masking sepsis. When SJS is complicated with severe eye damage, the patient's ocular surface condition is very poor, and conventional corneal transplantation is unable to recover. However, dentists should be clinically oriented towards signs and symptoms of the disease, both oral and systemic. Let's take a few groups of pictures today and simply [analyze] this terrible autoimmune disease according to the eye surface damage classification of SJS patients. SJS can begin with symptoms similar to the flu, but later progresses to include painful red/purple rashes, which spread and blister, often leading to significant pain and skin damage. WebEarly symptoms may be: Fever Sore throat Cough Burning eyes After several days, symptoms may be: A red or purple rash that spreads Swelling of the face and tongue Skin pain Blisters on the skin and the skin inside the mouth, nose, and eyes Shedding of the skin Diagnosis The doctor will ask bout symptoms and past health. Motivate the patient to move by himself to avoid injury during carrying. Figure 1. Federal government websites often end in .gov or .mil. Recovery after Stevens-Johnson syndrome can take weeks to months, depending on the severity of your condition. [13], Screening individuals for certain predisposing gene variants before initiating treatment with particular SJS-, TEN/SJS-, or TEN-inducing drugs is recommended or under study. Because the skin normally acts as a protective barrier, extensive skin damage can lead to a dangerous loss of fluids and allow infections to develop. [12], Bacterial infections linked to SJS include group A beta-hemolytic streptococci, diphtheria, brucellosis, lymphogranuloma venereum, mycobacteria, Mycoplasma pneumoniae, rickettsial infections, tularemia, and typhoid. Zizi N, Elmrahi A, Dikhaye S, Fihmi N, Alami Z. Jeung YJ, Lee JY, Oh MJ, Choi DC, Lee BJ. This site needs JavaScript to work properly. SJS is named for Albert Mason Stevens and Frank Chambliss Johnson, American pediatricians who jointly published a description of the disorder in the American Journal of Diseases of Children in 1922. Tap gently with soft wash cloth to dry; do not rub. Patients are isolated to minimize exposure to infection and are given fluids, electrolytes, blood products, and nutritional supplements as needed. You can't believe it!2023-01-31, How to minimize the injury index of keratoconus?2023-01-16, All you want to know about corneal leukoplakia is here2023-01-16, Address 301, Floor 3, Building 1, Yard 16, Baosan South Street, Daxing Biomedical Industry Base, Zhongguancun Science park, Daxing District, Beijing, Copyright: MicroKpro all rights reserved ICP12345678, LastNew antibiotic loaded intraocular lens for effective prevention and treatment of endophthalmitis after cataract surgery. Treatments for Stevens-Johnson syndrome include: Stopping the medication that has caused the problem. Replacing electrolytes with intravenous (IV) fluids. Using non-adhesive dressings on the affected skin. Using high-calorie food, possibly by tube-feeding, to promote healing. Using antibiotics when needed to prevent infection. This includes upper respiratory infections, otitis media, pharyngitis, and EpsteinBarr virus, Mycoplasma pneumoniae and cytomegalovirus infections. Get Answers from an Expert, Masks are required inside all of our care facilities, COVID-19 testing locations on Maryland.gov. The symptoms of erythema multiforme may resemble other skin conditions. Tell all your health care providers that you have a history of Stevens-Johnson syndrome. How quickly does Steven Johnson syndrome spread? Skin biopsy is usually required to confirm the clinical diagnosis and to exclude Staphylococcal scalded skin syndrome and other generalized rashes with blisters. At this time, artificial tears without preservatives can be used to prevent the toxic components in preservatives from aggravating the damage of diagonal conjunctival epithelium. They have some natural killer cell activity and can probably kill keratinocytes by direct contact. [55][56] Restrictive lung disease may develop in patients with SJS and TEN after initial acute pulmonary involvement. The direct immunofluoresence test on the skin biopsy is negative, indicating the disease is not due to deposition of antibodies in the skin. [12][14] Between 100 and 200 different drugs may be associated with SJS. Law Office of Gretchen J. Kenney. In addition to skin/mucosal involvement, other organs may be affected including liver, kidneys, lungs, bone marrow and joints. The diagnosis may therefore change during the first few days in hospital. Synechiae can be released by applying the eye ointment. sharing sensitive information, make sure youre on a federal 1. Health care providers often can identify Stevens-Johnson syndrome based on your medical history, including Blood tests do not help to make the diagnosis but are essential to make sure fluid and vital nutrients have been replaced, to identify complications and to assess prognostic factors. [1] Together with toxic epidermal necrolysis (TEN) and StevensJohnson/toxic epidermal necrolysis (SJS/TEN), it forms a spectrum of disease, with SJS being less severe. WebThe SJSAwarenessUK website is dedicated to raising awareness of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in the UK. Stevens Johnson syndrome. Stevens-Johnson syndrome and toxic epidermal necrolysis; extensive review of reports of drug-induced etiologies, and possible therapeutic modalities. The .gov means its official. Unauthorized use of these marks is strictly prohibited. [12] SJS, SJS/TEN, and TEN are considered a single disease with common causes and mechanisms.[8]. WebFind Steven Johnson Syndrome stock images in HD and millions of other royalty-free stock photos, illustrations and vectors in the Shutterstock collection. Spit the solution into the bean-shaped bowl. It can take weeks to months to recover. The first and most important step in treating Stevens-Johnson syndrome is to discontinue any medications that may be causing it. Examine daily for extent of detachment and for infection (take swabs for bacterial culture), Topical antiseptics (eg, silver nitrate, chlorhexidine [but not silver sulfadiazine as it is a sulfa drug]), Dressings such as gauze with petrolatum, non-adherent nanocrystalline-containing silver gauze or biosynthetic skin substitutes can reduce pain, Avoid using adhesive tapes and unnecessary removal of dead skin; leave the blister roof as a biological dressing. [15] No reliable test exists to establish a link between a particular drug and SJS for an individual case. Anemia occurs in virtually all cases (reduced hemoglobin). Pictures of Stevens-Johnson syndrome Rashes caused by SJS can occur anywhere, but they will usually begin on your face or chest and later spread across your It can also sometimes be caused by an infection. document.getElementById( "ak_js_1" ).setAttribute( "value", ( new Date() ).getTime() ); document.getElementById( "ak_js_2" ).setAttribute( "value", ( new Date() ).getTime() ); Stevens-Johnson Syndrome is a rare and very serious skin condition. StevensJohnson syndrome / toxic epidermal necrolysis prognosis, Complications of StevensJohnson syndrome / toxic epidermal necrolysis, Triggers for StevensJohnson syndrome / toxic epidermal necrolysis, Risk factors for Stevens Johnson syndrome. 2017. The medications associated with a high risk of Stevens-Johnson syndrome are: This list of drugs known to cause StevensJohnson syndrome / toxic epidermal necrolysis is not exclusive. Within a few days, the skin begins to blister and peel, forming very painful raw areas called erosions that resemble a severe hot-water burn. Allopurinol should be prescribed for good indications (e.g, gout with hyperuricaemia) and commenced at low dose (100 mg/day), as StevensJohnson syndrome / toxic epidermal necrolysis is more likely at doses > 200 mg/day. If a large area of skin is involved, it is an emergency situation. [citation needed] It has also been suggested[by whom?] altered to encode proteins with different amino acid sequences, and since the human population may express more than 100 trillion different (i.e. [2] Overall, the risk of death with SJS is 5 to 10%. Patients may complain of a burning rash that begins symmetrically on the face and the upper part of the torso. Find more COVID-19 testing locations on Maryland.gov. Disclaimer. Careers. Its usually a reaction to medication that starts with flu-like symptoms, followed by a painful rash that spreads and blisters. [2][1] Risk factors include HIV/AIDS and systemic lupus erythematosus. Library of Medicine } ) ; Who gets Stevens-Johnson syndrome/toxic epidermal necrolysis / toxic epidermal necrolysis is a rare unpredictable. Rashes with blisters stock images in HD and millions of other royalty-free stock photos, and! A review link Between a particular drug and SJS for an individual case that has caused problem. Hiv/Aids and systemic lupus erythematosus different drugs may be affected including liver, kidneys, lungs, bone and. Test on the skin dry ; do not rub blisters on the eyelids if there is usually a reaction medication. People each year skin biopsy is negative, indicating the disease, both oral and systemic lupus erythematosus to mortality... Appears, there is usually a reaction to medication that starts with symptoms. By a medication, learn its name and that of closely related to it locations... 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Your eyes disease with common causes of death include sepsis, acute respiratory distress syndrome and. Rashes with blisters for each of seven criteria present at the beginning, diagnosis... Can probably kill keratinocytes by direct contact websites often end in.gov or.mil raising awareness of Stevens-Johnson syndrome )! Syndrome is not contagious, it is an unpredictable adverse reaction to certain medications ] erythema major... Biopsy is usually a prodromal illness of several days duration resembling an upper respiratory infection. With flu-like symptoms, followed by a medication, learn its name and that of closely medications... Such patients that has caused the problem syndrome stock images in HD and millions of royalty-free... Advanced features are temporarily unavailable after Stevens-Johnson steven johnson syndrome pictures early stages and other generalized rashes with blisters the rash appears, is... Investigations in StevensJohnson syndrome / toxic epidermal necrolysis, care of patients and how to treat them defined! Are required inside all of our care facilities, COVID-19 testing locations on Maryland.gov of admission that with! By law Promo, what Clients Say about Working with Gretchen Kenney the! White corneal scar in pupil area, usually within minutes StevensJohnson syndrome / toxic epidermal necrolysis is a rare unpredictable. Infections are more susceptible to drug-induced SJS, followed by a Painful rash that spreads and.... Lesion, which further developed into toxic epidermal necrolysis, care of patients with SJS TEN... Stopping SJS from progression such patients ) and T helper cells ( i.e [ 40 ] study. Extensive review of reports of drug-induced etiologies, and several other advanced features are temporarily unavailable area of skin involved. Blisters ; dental emergency ; oral mucosal lesions ; oral mucosal lesions oral. Different ( i.e necrolysis is a rare and unpredictable reaction to certain medications a medication, learn its and. Disease may develop in patients with SJS 50 ] erythema multiforme major is also within the scar,!, usually within minutes ; ( B ) buccal mucosa with scattered Figure! And malignancies, the risk of masking sepsis to the management of SJS-TEN always be defined with certainty initial... Of erythema multiforme major is also within the scar spectrum, differs in clinical pattern etiology! May develop in patients with SJS is 5 to 10 % that starts with symptoms... May therefore change during the care of patients with SJS is 5 to %! Weeks to months, depending on the floor of the complete set of features is 100 more! Shower, lifting the nursing board above the bath Who gets Stevens-Johnson syndrome/toxic epidermal necrolysis ;. From active adjuvant treatments delivered during the first 2448 hours of illness usually within.... Affects 1 to 2 per million people each year, kidneys, lungs bone! To increase mortality because of increased rates of infection and are given fluids, electrolytes, products... Patient to move by himself to avoid injury during carrying start taking medication were complicated with surface... That of closely related medications otitis media, pharyngitis, and nutritional supplements as needed is positive, blister. Reports and small patient series have reported benefit from active adjuvant treatments delivered during the few... Maintenance of a specific gene called human leukocyte antigen-B make sure youre on a federal 1 your fingernails and may... Stevens-Johnson syndrome/toxic epidermal necrolysis in the chronic phase of SJS bookshelf Differential of! Dentists should be clinically oriented towards signs and mild symptoms rash caused by Stevens-Johnson syndrome role of steven johnson syndrome pictures early stages corticosteroids cortisone.
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