About Erythema Nodosum | ||
Erythema nodosum (EN) is an acute,
nodular, erythematous eruption that usually is limited to the extensor
aspects of the lower legs. Chronic or recurrent EN is rare but may
occur. EN is presumed to be a hypersensitivity reaction and may occur
in association with several systemic diseases or drug therapies, or it
may be idiopathic. The inflammatory reaction occurs in the panniculus. |
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EN probably is a
delayed
hypersensitivity reaction to a variety of antigens; circulating immune
complexes have not been found in idiopathic or uncomplicated cases,
however they may be demonstrated in patients with inflammatory bowel
disease. |
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Frequency: In the US: Peak incidence occurs at age 18-34 years. Age and sex distributions vary according to etiology and geographic location. Internationally: Rates of EN vary according to country. In England, the rate is 2.4 cases per 10,000 per year. Mortality/Morbidity: In most patients, EN resolves without any adverse reactions. Sex: Women are affected more often than men, with a male-to-female ratio of 1:4. Age: EN may occur in children and in patients older than 70 years, but it is more common in young adults aged 18-34 years. Age distribution varies with geographic location and etiology. |
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History: The eruptive phase of EN begins with flulike symptoms of fever and
generalized aching. Arthralgia may occur and precedes the eruption or appears during the
eruptive phase. Most lesions in infection-induced EN heal within 7 weeks, but active
disease may last up to 18 weeks. In contrast, 30% of idiopathic EN
cases may last more than 6 months. Febrile illness with dermatologic findings includes abrupt onset of
illness with initial fever, followed by a painful rash within 1-2 days |
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Physical:
Pertinent physical findings are limited to the skin and joints.
Distribution of skin lesions:
Characteristically, lesions appear on the
anterior leg; however, they may appear on any surface. Lesions change color in the second week from
bright red to bluish or livid. As absorption progresses, the color
gradually fades to a yellowish hue, resembling a bruise. This
disappears in 1 or 2 weeks as the overlying skin desquamates. Hilar adenopathy may develop as part of the
hypersensitivity reaction of EN. Bilateral hilar lymphadenopathy is
associated with sarcoidosis, while unilateral changes may occur with
infections and malignancy. Arthralgia occurs in more than 50% of patients and begins
during the eruptive phase or precedes the eruption by 2-4 weeks.
Erythema, swelling, and tenderness occur over the joint, sometimes with
effusions. Joint tenderness and morning stiffness may occur. Any joint
may be involved, but the ankles, knees, and wrist are affected most
commonly. Synovitis resolves within a few weeks, but joint pain and
stiffness may last up to 6 months. No destructive joint changes occur.
Synovial fluid is acellular, and the rheumatoid factor is negative. |
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Causes:
Currently, the most common cause of EN is streptococcal infection in
children and streptococcal infection and sarcoidosis in adults.
Numerous other causes have been reported. The causes reported most
often in the literature are as follows:
Bacterial infections include the following
Streptococcal infections: These infections are one of the most common
causes of EN.
Tuberculosis: An important cause in the past, tuberculosis has
decreased dramatically as a cause for EN but still must be excluded.Yersinia enterocolitica: This gram-negative bacillus causes acute diarrhea and abdominal pain and is a common cause of EN in France and Finland. Mycoplasma pneumoniae infection may cause EN. Leprosy: Clinically, erythema nodosum leprosum resembles EN, but the histologic picture is that of leukocytoclastic vasculitis. Lymphogranuloma venereum may cause EN. Salmonella infection may cause EN. Campylobacter infection may cause EN. |
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