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Brazilian Journal of Infectious Diseases

Print version ISSN 1413-8670

Braz J Infect Dis vol.14 no.6 Salvador Nov./Dec. 2010

http://dx.doi.org/10.1590/S1413-86702010000600014 

CASE REPORT

 

Candida tropicalis as an emerging pathogen in Candida meningitis: case report and review

 

 

Luciano Z GoldaniI; Rodrigo P SantosII

IInfectious Diseases Unit, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Brazil
IIInfectious Diseases Unit, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Brazil

Correspondence to

 

 


ABSTRACT

Candida species are an uncommon cause of meninigitis. Given the rarity of this infection, the epidemiology, prognosis, and optimal therapy for Candida meningitis are poorly defined. The authors report on a paraplegic patient due to spinal cord injury who developed C. tropicalis meningitis. In addition, we review and discuss other reported cases of C. tropicalis meningitis in the medical literature.

Keywords: Candida; meningitis.


 

 

INTRODUCTION

Candida species are an uncommon cause of meningitis. Given the rarity of this infection, the epidemiology, prognosis, and optimal therapy of Candida meningitis are poorly defined. Risk factors for meningitis are similar to those associated with invasive candidiasis. The risk of developing this complication is unknown. It occurs in immunosupressed patients, in patients treated with broad-spectrum antibiotics and receiving parenteral nutrition or result of disseminated disease.1-4 In addition, two specific patient groups, premature neonates and neurosurgical patients, are at increased risk.

The case of a paraplegic patient due to a spinal cord injury who developed C. tropicalis meningitis is herein reported and the cases reported in the medical literature are reviewed and discussed medical literature.

 

CASE REPORT

A 26-year-old man was admitted to Hospital das Clínicas, Porto Alegre, Brazil, in February 2009 complaining of nausea, vomiting, headache and fever (39ºC). Physical exam revealed neck stiffness without any focal neurological signs. Previous medical history included paraplegia due to a spinal injury (2002), decubitus ulcers (2002), pelvic osteomyelitis (2006) and recurrent urinary tract infections. A lumbar puncture yielded cerebrospinal fluid (CSF) with 2,500 leukocytes/mm3 (100% neutrophils), an elevated protein level of 98 mg/dL, and a reduced glucose level of 34 mg/dL. No fungi and bacteria were seen on Gram stain. CSF cultures were negative for bacteria and fungi. Chest-X ray, head CT scan, and transesophageal echocardiogram results were normal. Blood cultures and HIV serologic test results were negative. Urine cultures grew a mixed flora of Gram-positives and negatives, but urinary Gram-stain revealed innumerous yeasts compatible with Candida spp. Despite broad-spectrum 96-hours antibiotic therapy including cefepime, vancomycin, and metronidazole, the patient persisted with fever and headache. Repeated lumbar puncture showed 106 leukocytes/mm3 (70% neutrophils, 30% lymphocytes), a protein level of 40 mg/dL, and a glucose level of 24 mg/dL. At 24 hours, the primary plates and broth culture grew a budding yeast that was identified with a 99% probability as C. tropicalis on API 20C (bioMérieux). The isolates fluconazole MIC was 0.025 µg/mL on disk diffusion susceptibility testing. The patient was treated with amphotericin B deoxycholate (1.0 mg/kg/day) for five days but progressed to respiratory insufficiency, coma and death.

 

DISCUSSION

C. albicans accounts for 70%–100% of all fungal meningitis isolates.3,4 Other reported species include C. glabrata, C. tropicalis, C. parapsilopsis, and C. lusitaniae. As shown in Table 1, there have been few cases of C. tropicalis meningitis described in the medical literature.4-17 In contrast to meningitis caused by C. albicans, C. tropicalis meningitis has been increasingly reported in adults. Most cases of C. tropicalis are postoperative complications of head and neck surgery, including mastoid exploration, craniotomy, and ventricular-peritoneal shunt. Additional cases of C. tropicalis meningitis in adults have been reported in immunosupressed patients, patients taking prolonged broad-spectrum antibiotic therapy or as a result of disseminated disease, as observed in our case, which developed a possible Candida urinary tract infection with later dissemination to the central nervous system.

Symptoms such as those presented by our patient are similar to other Candida meningitis and include fever, headache, altered mental status, and meningism. Focal neurologic signs are rare. The diagnosis of meningitis is established by a positive CSF culture. Multiple CSF specimens may be required. CSF parameters are variable, with a mild lymphocytic or polymorphonuclear pleocytosis and an increased protein level. Fungal elements are generally not seen. Thus, CSF abnormalities are indistinguishable from cryptococcal, tuberculous, and some bacterial meningitides. Although fluconazole resistant isolates of C. tropicalis have been occasionally reported, the isolate of our case was fluconazole-susceptible.

Despite appropriate therapy with amphotericin B plus 5´fluorocytocine, mortality was seen in 5 of 17 patients (30%) with C. tropicalis meningitis. In addition to head and neck postoperative procedures, physicians should have a high index of suspicion for Candida meningitis in patients taking broad-spectrum antibiotics who also present an initial source of Candida infection. Non-albicans species identification and appropriate susceptibility tests should be considered for appropriate management of Candida meningitis.

 

REFERENCES

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Correspondence to:
Dr. Luciano Z. Goldani
Infectious Diseases Unit Hospital de Clínicas de Porto Alegre
Ramiro Barcelos 2350
Porto Alegre, 900640-003 Brazil

Submitted on: 03/05/2010
Approved on: 05/21/2010
We declare no conflict of interest.

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