A fatal case of Trichosporon inkin prosthetic endocarditis is reported. The isolation sites and susceptibility profiles of 10 other isolates are also reviewed. Four strains were recovered from cutaneous or subcutaneous samples, four were recovered from urine, one was recovered from peritoneal liquid, and one was recovered from bone. Voriconazole and amphotericin B had the most potent activities in vitro against the isolates, with MIC geometric means of 0.11 and 0.30 g/ml, respectively.
CASE REPORTA 52-year-old male underwent biological valve replacement for an insufficient aortic valve in October 1987. In May 2001, he developed valvular dysfunction with heart failure, and a second aortic valve replacement was performed. Fifteen months later, the patient presented to the Emergency Department with skin lesions on both hands, swelling of the right wrist, and articular pain. Physical examination revealed a temperature of 37.8°C and a leukocyte count of 12.8 ϫ10 6 per liter. Blood culture samples were taken, and the patient was discharged with the diagnosis of cellulitis and placed on amoxicillin-clavulanate therapy. Two days later, he came to the Infectious Diseases outpatient clinic with new skin lesions. An examination showed Osler's nodes in the fingers of both hands and in the feet and splinter hemorrhages on the nail folds. Transthoracic echocardiography showed a huge vegetation along the rim of the prosthetic aortic valve. After two new sets of blood cultures were performed, antibiotic therapy with vancomycin (1 g/12 h), gentamicin (80 mg/8 h), and rifampin (600 mg/day) was instituted. Forty-two hours later, the patient developed left hemiparesis and was transferred to another hospital for cardiovascular surgery. Unfortunately, after another 30 hours, he suffered a cardiopulmonary arrest and died before the surgery could be performed. An autopsy was not done.No growth was detected in the broth blood cultures after 7 days of incubation, but subcultures on Sabouraud glucose agar with gentamicin and chloramphenicol yielded colonies of a cream-colored organism after 48 h of incubation. Microscopic examination revealed budding cells and arthroconidia. Urease activity was positive. The API ID32C clinical yeast identification system (Biomerieux SA, Marcy-L'Etoile, France) was used to identify the isolate. With this commercial kit, we obtained the code 525764371, which is listed in the API ID32C database as a very good identification of Trichosporon inkin. However, the strain did not show growth on N-acetylglucosamine (the carbon source), a test by which the majority of T. inkin strains included in the API database are positive. Therefore, the isolate was sent to the Mycology Laboratory of the National Center for Microbiology of Spain for definitive identification and susceptibility testing.Identification of the isolate. At the National Center for Microbiology, the strain was labeled as CNM-CL-4811 (Spanish Centro Nacional de Microbiología yeast culture collection). The isolate was identified by routine physiological ...