Leprosy is a chronic, systemic infection characterized by progressive cutaneous lesions. It's sometimes called Hansen's disease. Ninety percent of leprosy cases in the United States are found in immigrants from leprosy-endemic regions (Mexico, India, and Southeast Asia). Incubation time is frequently 3 to 5 years but has been reported 6 months to several decades. It's commonly transmitted by humans, but a few cases have been transmitted from animals (armadillos and primates).
With timely and correct treatment, this seldom fatal disease has a good prognosis. Acute episodes may intensify leprosy's slowly progressing course, but whether such exacerbations are part of the disease process or a reaction to therapy remains unclear.
Untreated, leprosy can cause severe disability, blindness, and deformities. Leprosy takes three distinct forms:
Leprosy is a chronic disease caused by a bacillus, Mycobacterium leprae. M. leprae multiplies very slowly and the incubation period of the disease is about five years. Symptoms can take as long as 20 years to appear. Leprosy is not highly infectious. It is transmitted via droplets, from the nose and mouth, during close and frequent contacts with untreated cases.
Symptoms and Signs
Identification of acid-fast bacilli in skin and nasal mucosa scrapings confirms a diagnosis of leprosy. A skin biopsy shows the typical histologic pattern of nerve changes. The skin biopsy and scrapings also are evaluated to determine the percentage of fully intact cells (morphologic index) and to measure the amount of bacteria present (bacterial index).
Leprosy usually responds to antimicrobial therapy with sulfones, primarily oral dapsone, which may cause hypersensitivity reactions. Especially dangerous - but rare - reactions include hepatitis and exfoliative dermatitis. If these reactions occur, sulfone therapy should stop at once.
If leprosy fails to respond to sulfones or if the patient has respiratory or other complications, an alternative therapy, such as rifampin or clofazimine, may be effective.
Plantar ulcers are prevented by having the patient wear rigid-soled footwear or walking plaster casts. Contractures of the hand may be prevented by physical therapy. Reconstructive surgery is sometimes helpful. Nerve and tendon transplants and release of contractures also increase function. Plastic surgery for facial deformities may be needed. Ophthalmologic examinations should be done for all patients because 48% have evidence of sightthreatening ocular complications.
Prevention consists of avoiding close physical contact with untreated people. People on long-term medication become noninfectious.
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