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For further information, see CMDT PART 6-47: ERYTHEMA NODOSUM
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Essentials of Diagnosis
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Painful red nodules without ulceration on anterior aspects of legs
Slow regression over several weeks to resemble contusions
Women are predominantly affected by a ratio of 10:1 over men
Some cases associated with infection, inflammatory bowel disease, or drug sensitivity
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General Considerations
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Most cases are idiopathic; however, erythema nodosum can be a sign of systemic disease
The disease may be associated with various infectious and noninfectious conditions
Infection: streptococcal, coccidioidomycosis, other fungal (eg, histoplasmosis, blastomycosis), tuberculosis, diverticulitis, syphilis, Yersinia enterocolitica
Other: sarcoidosis, medications (eg, oral contraceptives), inflammatory bowel disease, pregnancy, Behçet disease
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The subcutaneous swellings are exquisitely tender and may be preceded by fever, malaise, and arthralgia
They are most often located on the anterior surfaces of the legs below the knees but may occur on the arms, trunk, and face
The lesions, 1–10 cm in diameter, are at first pink to red; with regression, all the various hues seen in a contusion can be observed
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Differential Diagnosis
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Erythema induratum (associated with tuberculosis)
Nodular vasculitis
Erythema multiforme
Lupus panniculitis
Poststeroid panniculitis
Contusions or bruises
Sweet syndrome (acute febrile neutrophilic dermatosis)
Subcutaneous fat necrosis (associated with pancreatitis)
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History and Physical Examination
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History should include inquiring about medication exposures, prior upper respiratory infection, and diarrheal illness
Significant physical examination findings include symptoms of any deep fungal infection endemic to the area
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Partial protein derivative (PPD)
Blood interferon gamma release assay (such as QuantiFERON) (see Pulmonary Tuberculosis)
Two consecutive ASO/DNAse B titers at 2- to 4-week intervals
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See Table 6–2
First identify and treat the underlying cause
Primary therapy is with nonsteroidal anti-inflammatory drugs
Saturated solution of potassium iodide, 5–15 drops three times daily, may result in prompt involution in many cases
Systemic therapy directed against the lesions themselves may include use of corticosteroids unless contraindicated by associated infection
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It usually lasts about 6 weeks and may recur
If no underlying cause is found, a significant underlying illness (usually sarcoidosis) will develop in only a small percentage of patients over the next year
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