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Antimicrobial Agents and Chemotherapy, June 2004, p. 2341, Vol. 48, No. 6
0066-4804/04/$08.00+0 DOI: 10.1128/AAC.48.6.2341.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
| LETTER TO THE EDITOR |
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The patient took oral fluconazole (600 mg/day), but his symptoms persisted. A computed tomography scan of the head was normal, and repeat LP revealed no improvement in CSF parameters. Fluconazole was stopped, and intravenous amphotericin B deoxycholate (AMB-DOC) was begun. Within 72 h, the patient developed acute nonoliguric renal failure. Amphotericin B lipid complex (ABLC) (5 mg/kg of body weight/day) was substituted for AMB-DOC. The patient's headaches and creatinine improved gradually. ABLC was discontinued, and oral fluconazole (600 mg/day) was begun.
The patient subsequently moved to Chicago, Ill. During the next 6 months he continued to have headaches associated with elevations in both CSF white blood cell count and titers of anti-Coccidioides antibody. Treatment with high doses of liposomal amphotericin B (up to 10 mg/kg/day) or fluconazole (1,200 mg/day) resulted in only partial clinical improvement. An Ommaya reservoir was placed, and escalating daily doses of intraventricular AMB were begun (up to 1 mg/day). Neurologic toxicity (nausea, vomiting, diplopia, headache, and tremor) secondary to intraventricular AMB developed and persisted despite reduction in both dose and frequency of intraventricular AMB. This was discontinued, and high-dose oral voriconazole (400 mg twice daily) was begun, after which the headaches resolved. The patient initially complained of solar photosensitivity, but this improved with the use of sunblock.
Two months later, evaluation of complaints of low back pain resulted in diagnosis of an intradural abscess at T11. The lesion, suspected to be a coccidioidomycoma, was surgically excised, but stains and cultures were negative. Surgery was complicated by communicating hydrocephalus, requiring ventriculo-peritoneal shunt placement.
After 21/2 years of treatment with voriconazole, the patient's headaches and back pain have resolved. Follow-up LPs reveal normal CSF cell counts, protein, and glucose. Serum and CSF anti-Coccidioides (by LP) antibodies by CF have remained undetectable (titers of <1:1). This patient's dose of voriconazole has been reduced to 200 mg twice daily, and lifelong therapy is planned.
Meningitis is a rare complication of infection with the fungus Coccidioides. Since this patient acquired his infection while in Arizona, he was presumed to have been infected with Coccidioides posadasii, which has recently been identified as the etiology of coccidioidomycosis outside of California (3). It is not known whether C. posadasii responds differently to fluconazole therapy than Coccidioides immitis. The treatment of Coccidioides meningitis can be difficult. Untreated infection is associated with nearly 100% mortality. There is doubt as to whether meningeal coccidioidomycosis is curable, and some authorities recommend lifelong antifungal therapy to prevent recurrence (2).
Although not approved for the treatment of the endemic mycoses, voriconazole has in vitro activity against these fungi, including C. immitis (5). Voriconazole has 96% oral bioavailability, low protein binding, and extensive tissue distribution, including penetration into the central nervous system (4). Voriconazole may be effective in patients with refractory coccidioidomycosis (1), including possibly infections due to C. posadasii. Further clinical studies are warranted.
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Laurie A. Proia Allan R. Tenorio* Department of Internal Medicine Section of Infectious Diseases Rush Medical College 600 South Paulina Suite 143 Academic Facility Chicago, IL 60612
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| * Phone: (312) 942-5865, Fax: (312) 942-8200, E-mail: allan_s_tenorio{at}rush.edu |
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