Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Toxic Epidermal Necrolysis 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.
- Acute Toxic Epidermolysis
- Dermatitis Exfoliativa
- Lyell Syndrome
- Ritter Disease
- Ritter-Lyell Syndrome
- Scalded Skin Syndrome
- Staphyloccal Scalded Skin Syndrome
- Toxic Epidermal Necrolysis
- Lyelles Syndrome
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
- Staphylococcal Scalded Skin Syndrome
- Stevens-Johnson Syndrome
Toxic epidermal necrolysis (TEN) is a rare, sometimes life-threatening unless properly treated, immunological disorder of the skin. It is characterized by blisters that meld into one another to cover a substantial portion of the body (30% and more), and extensive peeling or sloughing off of skin (exfoliation and denudation). The exposed under layer of skin (dermis) is red and suggests severe scalding. Often, the mucous membranes become involved, especially around the eyes (conjunctivitis), but also the mouth, throat, and bronchial tree.
Onset can occur at any age. The infantile form frequently follows an infection. In adults the disorder is usually caused by a reaction to taking a pharmaceutical drug, especially anticonvulsants, non-steroid anti-inflammatories, and/or some antibiotics.
TEN is thought to be an immunological disorder and to be one of a family of three skin disorders. TEN is considered to be the more serious, followed by Stevens-Johnson syndrome and erythema multiforme, in order of severity of disease.
Early in the course of the disorder, the major complaint is that of pain associated with a rash. Discrete, warm, red, measle-like spots appear and then merge to cover an extensive portion of the body. It is common to have a period of two or three days of general discomfort and fatigue (malaise), rash, fever, sore throat, and loss of appetite. Loss of appetite may, in part at least, be due to the involvement of the mucous membranes of the mouth and throat that makes eating and swallowing difficult. An acute phase (8-12 days) follows, during which the eyes become involved in the form of conjunctivitis. If this is not treated early and properly, loss of vision may result.
Development of crusted lesions around mucous membranes in the nose, ears, anus and/or vagina can be followed within 24 hours by intense redness in these areas. Skin redness may spread with tenderness, itching and separation of skin layers possibly developing within 36 to 48 hours. Apparently normal skin may peel away in large sheets when touched (Nikolsky's sign). Blisters of various sizes may form, along with peeling. The severity of peeling skin is often related to the degree of fever, severe discomfort, and loss of appetite. With healing, peeled areas may become dried and yellowish crusts may appear in affected areas.
Toxic epidermal necrolysis usually progresses rapidly and within a few days may become severe. After extensive peeling, fluid loss that can lead to dehydration, giving rise to signs and symptoms not unlike those that occur in burn victims. Disfiguring scarring, also resembling the scars associated with burns, may develop when the skin begins to heal.
Among infants or children, TEN is often caused by bacterial (staphylococcal) infections. A common staphylococcal skin infection with blisters and crusting called Impetigo may also precede this disorder. Toxic epidermal necrolysis can occur sporadically or in epidemic proportions in nurseries.
An allergic reaction to a drug is most often the cause among adults. The exact cause of the violent skin reaction is unknown. There appears to be an immune response leading to the rejection of the skin and mucous membrane. Most cases involve the use of medications such as antibacterial sulfonamides (chloramphenicol), non-steroidal anti-inflammatory drugs (including ibuprofen), and anticonvulsants such as phenytoin.
Some clinicians believe that genetic defects in the patient's metabolic pathways lead to the accumulation of toxic metabolites. They propose that a break occurs in the body's self-tolerance of proteins that the body itself produces.
In the United States, it has been estimated that TEN occurs in 0.22 to 1.23 cases per 100,000 of population. It seems to affect males and females in equal numbers.
At one time TEN was fatal in about 40% of cases. However with proper treatment in a burn center or intensive care center, the rate of mortality has dropped to 20%. For unknown reasons, TEN affects more women than men. The female to male ratio is 1.6:1. The age distribution of persons with TEN appears to be skewed towards the elderly, but that may be because the elderly take more medications than do younger people.
Symptoms of the following disorders can be similar to those of toxic epidermal necrolysis. Comparisons may be useful for a differential diagnosis:
Staphylococcal scalded skin syndrome (SSSS) is also a disorder characterized by red blistering skin that looks like a burn or scald, hence the name. SSSS is caused by the release of two toxins (epidermolytic toxins A and B) from particular strains of the bacteria Staphylococcus aureus. These toxins disrupt the parts of skin cells responsible for making the cells stick to each other. The cells become unstuck and therefore "peel".
Stevens-Johnson syndrome is another blistering skin disorder usually affecting children and young adults. It is marked by severe reddening and blisters on the skin and mucous membranes. A preliminary stage may last from one to two weeks consisting of fever, discomfort, coughing linked to an acute allergic reaction, sore throat, chest pain, vomiting, diarrhea, and joint or muscle pain. Lesions may then appear in the mouth and throat as well as on reproductive organs and the anal area. Progressive eye inflammation can lead to diminished vision. Crusting with bleeding may develop on the lips. Symptoms may heal within three to six weeks, but can recur at any time. The cause of this disorder is not known, although more severe cases are possibly associated with collagen disease, malignancy, contact dermatitis or drug reactions. Stevens-Johnson usually appears in the fall or spring, for reasons not yet understood by scientists. (For more information on this disorder, choose "Stevens-Johnson" as your search term in the Rare Disease Database.)
Rapid recognition, diagnosis, and the appropriate site of treatment are essential in order to minimize the potentially dangerous consequences of this disorder in children or adults. If the patient cannot be treated at a specialized burn unit, treatment may then best take place in an intensive care unit. TEN, as well as Stevens-Johnson syndrome, are clinically evident, but the diagnosis may be confirmed by immunofluorescence studies, skin biopsy to determine the depth at which the skin is peeling, and bacterial studies in the case of children.
If peeling takes place when the upper layers of the skin slip free of the lower layers upon being rubbed with only slight pressure, that may be an indicator of toxic epidermal necrolysis.
Early treatment of infantile or childhood onset toxic epidermal necrolysis is essential because of the rapid progression of symptoms. Antibiotic (e.g., penicillin) drug therapy may be helpful for treatment of infection. Fluid and electrolyte balance may need correction. Children should be watched carefully to prevent them from touching peeled or blistered areas, and possibly worsening the condition. Hospitalization and/or isolation may be required to assure a sterile environment. Healing may rapidly follow appropriate treatment.
Treatment of adult onset toxic epidermal necrolysis is usually similar to therapy for severe burns. Immediate removal of the offending drug is a key to treatment. Contact with peeled skin surface should be minimal. Hospitalization with isolation in a sterile environment to minimize infection may be necessary. Severe loss of fluid and electrolytes may require replacement on an ongoing basis to prevent dehydration. If the disorder is caused by a drug reaction, systemic corticosteroids may be able to control the reaction but do not seem to improve skin symptoms. Blood poisoning and lung infections should be anticipated and treated promptly if they occur. Other therapy is symptomatic and supportive.
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FROM THE INTERNET
Ngan V. Toxic epidermal necrolysis. Dermnet.Last updated: 30 March 2003. 3pp.
Lehrer M. Erythema multiforme. Medical Encyclopedia, MedlinePlus. Update Date: 7/28/2001. 4 pp.
Toxic Epidermal Necrolysis. Lucille Packard Children's Hospital. nd. 2pp.
Stevens Johnson Syndrome Foundation. Stevens Johnson Syndrome/Toxic Epidermal Necrolysis. nd. 2pp.
Dystrophic Epidermolysis Bullosa Research Association of America, Inc. (DEBRA)
75 Broad Street
New York, NY 10004
NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases
One AMS Circle
Bethesda, MD 20892-3675
University of Pennsylvania Dermatology Clinic
34th and Spruce Streets
Philadelphia, PA 19104
Stevens Johnson Syndrome Foundation and Support Group
PO Box 350333
Westminster, CO 80035-0333
Genetic and Rare Diseases (GARD) Information Center
PO Box 8126
Gaithersburg, MD 20898-8126
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