Curvularia infections in humans are relatively uncommon despite the ubiquitous presence of this soildwelling dematiaceous fungus in the environment. Originally thought to be solely a pathogen of plants, Curvularia has been described as a pathogen of humans and animals in the last half-century, causing respiratory tract, cutaneous, and corneal infections. Only three previous cases of central nervous system involvement by Curvularia have been documented in the medical literature. We report a fatal case of cerebral Curvularia infection in which there was no known history of immunocompromise or prior respiratory tract or sinus infection in the patient.
CASE REPORTA 21-year-old African-American male with a past medical history significant only for asthma presented to our medical center complaining of headache for the previous 2 months. The headache was located in the parietal and occipital regions and was constant with increasing severity over the past month. He obtained no relief with the use of over-the-counter medications. The headache was associated with double vision, dizziness, unsteady gait, anorexia with a 10-pound weight loss, low-grade fever, chills, and night sweats. His social history included smoking one pack of cigarettes per day and occasional cocaine and marijuana use. He denied intravenous drug use and was taking no medications at the time of admission. Physical examination findings included a temperature of 100.4°F; blood pressure of 101/67 mm Hg; neurologic status, alert and oriented to person, place, and time; no nuchal rigidity; no neurologic deficits; and diffuse inspiratory and expiratory wheezes bilaterally. Laboratory findings included a normal complete blood count, a urine drug screen positive for barbiturates and cannabinoids, and a slightly decreased serum sodium level. A computed tomography (CT) scan of the brain with and without contrast revealed a 4.8-by 3.8-cm area of intraparenchymal hypodensity on the right side of the brain involving the right basal ganglia and anterior horn adjacent to the right lateral ventricle with a density suggestive of hemorrhage. Apparent cerebral edema with a 4.0-mm left midline shift was also noted.The patient was admitted to the intensive care unit and begun on mannitol and dexamethasone to reduce intracranial swelling. A stereotactic needle aspiration and biopsy of the cerebral mass was performed 2 days later. Cytologic analysis of the aspirated material showed rare pleomorphic septate fungal elements in a background of neutrophils, lymphocytes, multinucleated histiocytes, and necrotic debris (Fig. 1). Histologic sections of the stereotactic brain biopsy tissue demonstrated brain parenchyma with granulomatous inflammation and necrosis associated with scattered light-brown fungal hyphae (Fig. 2). The fungal hyphae in the biopsy specimen were much more uniform in diameter than those seen in the fluid sample. Only rare septa were identified. Treatment of the patient with amphotericin B, vancomycin, and ceftriaxone was begun. Culture of the biopsy tissue sub...