Stevens Johnson Syndrome

Stevens Johnson Syndrome

National Organization for Rare Disorders, Inc.

Important

It is possible that the main title of the report Stevens Johnson Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.

Synonyms

  • Dermatostomatitis, Stevens Johnson Type
  • Ectodermosis Erosiva Pluriorificialis
  • Erythema Multiforme Exudativum
  • Erythema Polymorphe, Stevens Johnson Type
  • Febrile Mucocutaneous Syndrome, Stevens Johnson Type
  • Herpes Iris, Stevens-Johnson Type
  • Johnson-Stevens Disease

Disorder Subdivisions

  • None

General Discussion

Until recently the relationship of Stevens-Johnson syndrome to other severe blistering disorders was a matter of some debate. Now a consensus seems to be evolving that describes SJS as a rare disorder involving lesions of the mucous membranes along with small blisters on the reddish or purplish, flat, thickened patches of skin. As a result, SJS is now distinguished as a separate disorder from erythema multiforme major (EMM). SJS is now considered to be a less severe variant of toxic epidermal necrolysis (TEN).



SJS and TEN appear to be characterized by identical clinical signs and symptoms, identical treatment approach and identical prognosis. Patients diagnosed with TEN can present with symptoms ranging from 10% skin involvement and severe threat to the patient's sight to a presentation involving 90% of the skin but only a modest threat to the patient's sight.



SJS (and TEN) is an inflammatory disorder of the skin triggered by an allergic reaction to certain drugs including antibiotics, such as some sulfonamides, tetracycline, amoxicillin, and ampicillin. In some cases, nonsteroidal anti-inflammatory medications and anticonvulsants, such as Tegretol and phenobarbital have also been implicated. Over-the-counter medications may act as triggers as well. In some cases, it is also possible that the disorder may be traced to a reaction to an infection.



One report suggests that the term SJS be limited to cases in which less than 10% of the total body surface area is involved. The authors suggest that the term TEN be limited to cases in which 30% or more of the total body surface area is involved. The term SJS/TEN Overlap is used to describe patients in whom between 10-30% of the total body surface area involved.

Symptoms

Stevens-Johnson syndrome is a rare disorder characterized by inflammation of the skin and/or mucus membranes (mucocutaneous). Affected individuals may have abnormalities (lesions) of the skin and mucus membranes that are purplish or red in color. The abnormalities may be flat (macules) or small and raised (papules). In some cases, the lesions may develop raised fluid-filled centers (bullae or blisters). Affected individuals may also have blisters and/or bleeding in the mucous membranes of the lips, eyes, mouth, nasal passage, and genitals. A crust-like surface may form on the blisters, and in some cases, the blisters may be painful and/or itchy. Affected individuals may have difficulty swallowing and taking nourishment (impaired alimentation). In some cases, affected individuals may also have lesions of the stomach and/or intestine, which may contribute to impaired alimentation. The lesions may enter the respiratory tract and cause difficulty in breathing. The lesions may also form in the urinary tract, making it difficult for affected individuals to pass urine.



In addition, abnormalities of the eyes may develop as a result of the lesions caused by Stevens-Johnson Syndrome (ocular sequelae). Such abnormalities may include infection of the transparent membrane of the eye and eyelids (conjunctiva) and inflammation of associated with an abnormal discharge from the conjunctiva (purulent conjunctivitis). In some cases, the eyelid may be adhere to the eyeball (symblepharon) and/or tear (lacrimal gland) ducts may be blocked or damaged, which may lead to dry eyes (dry eye syndrome or keratoconjunctivitis sicca). The range and severity of symptoms may vary from case to case.

Causes

More than 50% of the cases of SJS have been traced to a reaction to a medication. However, there are no tests that predict the response of a person to a particular pharmaceutical. Over 100 drugs have been implicated. Sulfonamides account for most cases, about 30%. Anticonvulsants are the second most frequent cause of SJS. Many infectious agents have been implicated in the onset of SJS.



The cause of Stevens-Johnson syndrome is not fully understood. It is clear that in some way, the immune system intervenes in the process of metabolizing the drug against which the body reacts. The precursors (keratocytes) to the skin cells are affected and destroyed (necrosis) in this process. An abnormally large concentration of volatile and potentially poisonous intermediate metabolites accumulates, because the body's ability to detoxify these intermediate metabolites is reduced. At this point, it is suggested, the immune response is triggered and the dangerous skin reactions take place.



These actions are collectively called cell-mediated immune reactions.

Affected Populations

The incidence of SJS has been estimated at about 1.2 to 6.0 cases per million of population per year. Risk factors include HIV disease, bone marrow transplantation, graft vs host disease and systemic lupus. Before the HIV epidemic there were slightly more females than males affected by the disorder. Currently, the incidence is approximately the same in males and females.



Severity of the disorder is directly related to the proportion of body surface affected.

Standard Therapies

Diagnosis

The diagnosis of SJS depends on a thorough history, especially of the use of medications. The mucocutaneous lesions are readily recognized.



Treatment

When a cause for Stevens-Johnson syndrome can be found, it should be treated by aggressively eliminating or avoiding drugs or other substances to which the patient is allergic). Local treatment depends on the type of lesion. Especially serious cases may require moving the patient to a burn-care center.



Infections of the lips and mouth may require special care. Intense oral hygiene is necessary. A mouthwash of sodium bicarbonate solution in warm water can be soothing and cleansing. Systemic corticosteroids are not advised and their use is to be avoided. Intensive systemic antibiotics, fluids and electrolytes may be lifesaving in patients with extensive mucous membrane lesions.



Ophthalmic consultation is required when the eyes are involved. Precautions must be taken to avoid permanent eye damage.

Investigational Therapies

Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.



For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:



Tollfree: (800) 411-1222

TTY: (866) 411-1010

Email: prpl@cc.nih.gov



For information about clinical trials sponsored by private sources, contact:

www.centerwatch.com

References

TEXTBOOKS

EshragiN, Stern RE, Faucher LD, et al. Toxic Epidermal Necrolysis. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:139-40.



Cohen BA. Erythema Multiforme. In: NORD Guide to Rare Disorders. Lippincott Williams & Wilkins. Philadelphia, PA. 2003:110-11.



Beers MH, Berkow R., eds. The Merck Manual, 17th ed. Whitehouse Station, NJ: Merck Research Laboratories; 1999:824.



Berkow R., ed. The Merck Manual-Home Edition.2nd ed. Whitehouse Station, NJ: Merck Research Laboratories; 2003:1199-200.



Frank MM, Austen KF, Claman HN, et al. Eds. Samter's Immunological Diseases. 5th ed. Little Brown and Company, Boston, MA; 1995:1193-97.



REVIEW ARTICLES

Jones DH, Todd M, Craig TJ. Early diagnosis is key in vancomycin-induced Linear IgA Bullous dermatosis and Stevens-Johnson syndrome. J Am Osteopath Assoc. 2004;104:157-63.



Hockett KC. Stevens-Johnson syndrome and toxic epidermal necrolysis: oncologic considerations. Clin J Oncol Nurs. 2004;8:27-30, 55.



Taylor WR, White NJ. Antimalarial drug toxicity: a review. Drug Saf. 2004;27:25-61.



Witkowski JA, Parish LC. Cutaneous reactions to antibacterial agents. Skinmed. 2002;1:25-61.



Metry DW, Jung P, Levy ML. Use of intravenous immunoglobulin in children with stevens-johnson syndrome and toxic epidermal necrolysis: seven cases and review of the literature. Pediatrics. 2003;112:1430-36.



Bachot N, Roujeau JC. Intravenous immunoglobulins in the treatment of severe drug eruptions. Curr Opin Allergy Clin Immunol. 2003;3:269-74.



Bachot N, Roujeau JC. Differential diagnosis of severe cutaneous drug eruptions. Am J Clin Dermatol. 2003;4:561-72.



Warnock JK, Morris DW. Adverse cutaneous reactions to mood stabilizers. Am J Clin Dermatol. 2003;4:21-30.



Ghislain PD, Roujeau JC. Treatment of severe drug reactions: Stevens-Johnson syndrome, toxic epidermal necrolysis, and hypersensitivity syndrome. Dermatol Online J. 2002;8:5.



JOURNAL ARTICLES

Chung WH, Hung SI, Hong HS, et al. A marker for Stevens-Johnson syndrome. Nature. 2004;428:486.



Nakamura T, Inatomi T, Sotozono C, et al. Transplantation of cultivated autologous oral mucosal epithelial cells in patients with severe ocular surface disorders. Br J Opthalmol. 2004;88:1280-84.



Nishida K, Yamato M, hayashida Y, et al. Corneal reconstruction with tissue- engineered cell sheets com[posed of autologous oral mucosal epithelium. N Engl J Med. 2004;351:1187-96.



Mockenhaupt M, Kelly JP, Kaufman D, et al. The risk of Stevens-Johnson syndrome and toxic epidermal necrolysis associated with nonsteroidal antiinflammatory drugs: a multinational perspective. J Rheumatol. 2003;30:2234-40.



FROM THE INTERNET

Revis DR. Erythema Multiforme (Stevens-Johnson Syndrome). emedicine. Last Updated: January 20, 2003. 14pp.

www.emedicine.com/med/topic727.htm



Foster CS, Letko E. Stevens-Johnson Syndrome. Last Updated: July 10, 2001. 14pp.

www.emedicine.com/oph/topic268.htm



Dixon J, Levine N. South American Blastomycosis. Last Updated: March 3, 2002. 18pp.

www.emedicine.com/derm/topic863.htm



Parillo SJ, Parillo CV. Stevens-Johnson Syndrome. Last Updated: September 22, 2004. 11pp.

www.emedicine.com/EMERG/topic555.htm



Erythema Multiforme. DermNet NZ. Last updated 01 Dec 2004. 2pp.

www.dermnetnz.org/reactions/erythema_multiforme.html



Toxic epidermal necrolysis. DermNet NZ. Last updated 03 Oct 2004. 3pp.

www.dermnetnz.org/reactions/toxic-epidermal-necrolysis.html



The facts about Stevens-Johnson Syndrome (SJS). ©2001 SJS Foundation. 1p.

www.sjssupport.org



New Treatment for Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis. American Academy of Ophthalmology. nd. 2pp.

www.aao.org/aao/education/library/memberalert/stevens_johnson.cfm



What is Stevens-Johnson Syndrome? KidsGrowth.com nd. 3pp.

www.kidsgrowth.com/resources/articledetail.cfm?id=979



Stevens-Johnson Syndrome. WrongDiagnosis.com. nd. 3pp.

www.weongdiagnosis.com/s/stevens_johnson_syndrome.htm

Resources

NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases

Information Clearinghouse

One AMS Circle

Bethesda, MD 20892-3675

USA

Tel: (301)495-4484

Fax: (301)718-6366

Tel: (877)226-4267

TDD: (301)565-2966

Email: NIAMSinfo@mail.nih.gov

Internet: http://www.niams.nih.gov/



NIH/National Eye Institute

31 Center Dr

MSC 2510

Bethesda, MD 20892-2510

United States

Tel: (301)496-5248

Fax: (301)402-1065

Email: 2020@nei.nih.gov

Internet: http://www.nei.nih.gov/



NIH/National Institute of Allergy and Infectious Diseases

Office of Communications and Government Relations

6610 Rockledge Drive, MSC 6612

Bethesda, MD 20892-6612

Tel: (301)496-5717

Fax: (301)402-3573

Tel: (866)284-4107

TDD: (800)877-8339

Email: ocpostoffice@niaid.nih.gov

Internet: http://www.niaid.nih.gov/



Stevens Johnson Syndrome Foundation and Support Group

PO Box 350333

Westminster, CO 80035-0333

Tel: (303)635-1241

Fax: (303)648-6686

Email: sjs@gmail.com

Internet: http://www.sjsupport.org



Genetic and Rare Diseases (GARD) Information Center

PO Box 8126

Gaithersburg, MD 20898-8126

Tel: (301)251-4925

Fax: (301)251-4911

Tel: (888)205-2311

TDD: (888)205-3223

Internet: http://rarediseases.info.nih.gov/GARD/



Madisons Foundation

PO Box 241956

Los Angeles, CA 90024

Tel: (310)264-0826

Fax: (310)264-4766

Email: getinfo@madisonsfoundation.org

Internet: http://www.madisonsfoundation.org



For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.

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