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Anthrax is an acute infectious disease caused by the gram-positive, encapsulated, nonmotile, spore-forming rod Bacillus anthracis.1,2 The incubation period is 1 to 7 days after exposure, and no person-to-person transmission is documented. Its potential as an agent of bioterrorism should prompt immediate notification of the local or state health department upon first suspicion of an anthrax-like illness. Human anthrax cases arise after exposure to infected animals or their products and rarely occur in the United States. In 2001, B anthracis spores intentionally delivered through the US Postal Serviceresulted in 22 cases of bioterrorism-related anthrax.3

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Clinical Manifestations

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Anthrax infections occur as cutaneous, inhaled, and gastrointestinal. All forms can progress to sepsis and meningitis. Cutaneous anthrax appears when B anthracis spores enter through a cutaneous abrasion.4 A small erythematous papule vesiculates to form a painless eschar with marked edema. Lymphadenopathy or lymphangitis may occur. Untreated, mortality is as high as 20%.

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Inhalation anthrax occurs after respiratory exposure to B anthracis spores.5 Initial symptoms are nonspecific, mimicking influenza. Symptoms become fulminant over a few days, often leading to death. Mediastinal widening on chest radiograph is pathognomonic. Hemorrhagic meningitis and bacteremia are common.

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Gastrointestinal anthrax follows ingestion of contaminated, undercooked meat,6 presenting with nausea, vomiting, and malaise, progressing to bloody diarrhea, gross ascites, hemorrhagic lymphadenitis, and sepsis. A pharyngeal form of anthrax occurs with profound submental swelling, adenopathy, and systemic symptoms.7 Multiple forms of anthrax have been described in children.8-15

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Diagnosis

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Gram stain and culture of vesicular fluid or blood confirm the diagnosis of anthrax. B anthracis grows in ordinary nutrient broth and on blood agar,2 appearing as large, gram-positive, sporulating bacilli on Gram stain. Rapid diagnostic tests are available through the Laboratory Response Network.16

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Treatment and Prevention

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Antibiotic resistance to penicillins and tetracyclines is assumed in bioterrorism cases until proven otherwise.1 Empiric therapy of inhalational or gastrointestinal bioterrorism-mediated anthrax includes intravenous ciprofloxacin or doxycycline plus 1 or 2 additional agents, including rifampin, vancomycin, penicillin, ampicillin, chloramphenicol, imipenem, clindamycin, and clarithromycin. Ciprofloxacin has better central nervous system penetration than doxycycline. First-line therapy for cutaneous anthrax includes either oral ciprofloxacin or doxycycline. If cutaneous lesions involve the head and neck or extensive edema is associated, combination intravenous regimens are recommended. Steroid therapy is considered for severe edema associated with cutaneous lesions and for meningitis. As spores may persist in the respiratory tract, all forms of anthrax are treated for 60 days, and therapy may be completed orally when clinically appropriate.17,18

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Treatment recommendations for children include ciprofloxacin (10 mg/kg/dose intravenously transitioning to 15 mg/kg/dose orally every 12 hours, maximum 500 mg per dose) or doxycycline (2.2 mg/kg/dose intravenously transitioning to same dose orally every 12 hours, maximum 100 mg per dose), plus 1 or 2 ...

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