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Nocardiosis is an acute or chronic, often disseminated,
suppurative or granulomatous infection caused by various
aerobic soil saprophytes of the genus Nocardia.
Pneumonia is typical, but skin and CNS infections are
common. Diagnosis is by culture and special stains.
Treatment is usually with sulfonamides.
Several Nocardia sp, in the family Actinomycetaceae,
cause human disease. The most common human pathogen is
N. asteroides, which usually causes pulmonary and
disseminated infection. N. brasiliensis most commonly
causes skin infection, particularly in tropical
climates. Infection is via inhalation or by direct
inoculation of the skin. Nocardiosis occurs worldwide in
all age groups, but incidence is greater among older
adults, especially men. Person-to-person spread is rare.
Lymphoreticular malignancies, organ transplantation,
high-dose corticosteroid or other immunosuppressive
therapy, and underlying pulmonary disease are
predisposing factors, but about 1⁄2 the patients have no
preexisting disease. Nocardiosis is also an
opportunistic infection in patients with advanced HIV
infection. Other Nocardia sp sometimes cause localized
or, occasionally, systemic infections.
Symptoms and Signs
Nocardiosis usually begins as a subacute pulmonary
infection that resembles actinomycosis, but Nocardia is
more likely to disseminate locally or hematogenously.
Dissemination with abscess formation may involve any
organ but most commonly affects the brain, skin, kidney,
bone, or muscle. |
The most common symptoms of pulmonary involvement—cough, fever,
chills, chest pain, weakness, anorexia, and weight loss—are
nonspecific and may resemble those of TB or suppurative
pneumonia. Pleural effusion also may occur. Metastatic brain
abscesses, occurring in 30 to 50% of cases, usually produce
severe headaches and focal neurologic abnormalities. Infection
may be acute, subacute, or chronic.
Skin or subcutaneous abscesses occur frequently, sometimes as a
primary local inoculation. They may appear as a firm cellulitis,
a lymphocutaneous syndrome, or an actinomycetoma. The
lymphocutaneous syndrome consists of a primary pyoderma lesion
and lymphatic nodules resembling sporotrichosis. An
actinomycetoma begins as a nodule, suppurates, spreads along
fascial planes, and drains through chronic fistulas.
Diagnosis
Diagnosis is by identification of Nocardia sp in tissue or
culture from localized lesions identified by physical
examination, x-ray, or other imaging studies. Clumps of beaded,
branching filaments of gram-positive bacteria (which may be
weakly acid-fast) are often seen. Nocardia do not develop a
clubbed appearance, as does Actinomyces israelii.
Prognosis and Treatment
Without treatment, pulmonary and disseminated nocardiosis are
usually fatal. Among patients who are treated with appropriate
antibiotics, the mortality rate is highest (> 50%) in
immunocompromised patients with disseminated infections and
lowest (about 10%) in immunocompetent patients with lesions
restricted to the lungs. Cure rates for patients with skin
infection are usually > 95%.
Trimethoprim-sulfamethoxazole or high doses of a sulfonamide
alone (sulfamethoxazole or sulfisoxazole) are used. Because most
cases respond slowly, a dose that maintains a sulfonamide blood
concentration of 12 to 15 mg/dL (eg, with sulfadiazine 4 to 6
g/day po) must be continued for several months. When sulfonamide
hypersensitivity or refractory infection is present, amikacin, a
tetracycline (particularly minocycline), imipenem-cilastatin,
ceftriaxone, cefotaxime, or cycloserine can be used. In vitro
susceptibility data should guide the choice of alternative
drugs.
Last full review/revision November
2005