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. 2003;11(2):131–133. doi: 10.1080/10647440300025510

Vulvovaginal Trichosporonosis

Paul Makela 1,, Debbie Leaman 2, Jack D Sobel 2
PMCID: PMC1852272  PMID: 14627220

Abstract

Objective: Isolation of Trichosporon species from vaginal secretions is a rare event, and no data are available on its pathogenic role. A case series is presented to determine the pathogenic role of Trichosporon species in vulvovaginal infections.

Methods: We performed a retrospective chart review of patients seen in the W.S.U. Vaginitis Clinic in order to identify patients from whom Trichosporon species were isolated.

Results: Between 1986 and 2001, a total of 13 patients had a total of 18 positive vaginal cultures for Trichosporon species. All 18 vaginal isolates were T. inkin. In general, positive vaginal cultures were accompanied by low yeast colony counts. Four out of 18 positive T. inkin cultures were obtained from visits by asymptomatic patients. Of the remaining 14 positive T. inkin cultures from patients with symptoms, nine out of 14 cultures had other diagnoses (Candida albicans, six cases; bacterial vaginosis, two cases; Trichomonas, one case). Five positive T. inkin cultures were obtained from visits at which patients had symptoms and no associated diagnosis. In only one of the five episodes could we establish a clear pathogenic role for Trichosporon. In this case the patient was treated with boric acid and had resolution of symptoms and a negative culture at follow-up. In-vitro susceptibility tests revealed that T. inkin was resistant to flucytosine and susceptible to all topical and oral azoles.

Conclusions: T. inkin is occasionally found in vulvovaginal cultures and is usually a non-pathogen. Transient colonization tended to occur in women, usually of African—American origin, with major perturbations in vaginal flora (bacterial vaginosis and trichomoniasis) and increased pH. Pathogenic consequences of Trichosporon colonization appear to be rare.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chaumentin G., Boibieux A., Piens M. A., Douchet C., Buttard P., Bertrand J. L., Peyramond D. Trichosporon inkin endocarditis: short-term evolution and clinical report. Clin Infect Dis. 1996 Aug;23(2):396–397. doi: 10.1093/clinids/23.2.396. [DOI] [PubMed] [Google Scholar]
  2. Guého E., Improvisi L., de Hoog G. S., Dupont B. Trichosporon on humans: a practical account. Mycoses. 1994 Jan-Feb;37(1-2):3–10. doi: 10.1111/j.1439-0507.1994.tb00277.x. [DOI] [PubMed] [Google Scholar]
  3. Guého E., Smith M. T., de Hoog G. S., Billon-Grand G., Christen R., Batenburg-van der Vegte W. H. Contributions to a revision of the genus Trichosporon. Antonie Van Leeuwenhoek. 1992 May;61(4):289–316. doi: 10.1007/BF00713938. [DOI] [PubMed] [Google Scholar]
  4. Itoh T., Hosokawa H., Kohdera U., Toyazaki N., Asada Y. Disseminated infection with Trichosporon asahii. Mycoses. 1996 May-Jun;39(5-6):195–199. doi: 10.1111/j.1439-0507.1996.tb00124.x. [DOI] [PubMed] [Google Scholar]
  5. Lopes J. O., Alves S. H., Klock C., Oliveira L. T., Dal Forno N. R. Trichosporon inkin peritonitis during continuous ambulatory peritoneal dialysis with bibliography review. Mycopathologia. 1997;139(1):15–18. doi: 10.1023/a:1006870017725. [DOI] [PubMed] [Google Scholar]
  6. Mayser P., Huppertz M., Papavassilis C., Gründer K. Hefen der Gattung Trichosporon. Identifizierung, Epidemiologie und Bedeutung der dermatologischen Krankheitsbilder. Hautarzt. 1996 Dec;47(12):913–920. doi: 10.1007/s001050050531. [DOI] [PubMed] [Google Scholar]
  7. Piwoz J. A., Stadtmauer G. J., Bottone E. J., Weitzman I., Shlasko E., Cummingham-Rundles C. Trichosporon inkin lung abscesses presenting as a penetrating chest wall mass. Pediatr Infect Dis J. 2000 Oct;19(10):1025–1027. doi: 10.1097/00006454-200010000-00023. [DOI] [PubMed] [Google Scholar]
  8. Sobel J. D. Epidemiology and pathogenesis of recurrent vulvovaginal candidiasis. Am J Obstet Gynecol. 1985 Aug 1;152(7 Pt 2):924–935. doi: 10.1016/s0002-9378(85)80003-x. [DOI] [PubMed] [Google Scholar]
  9. Sobel J. D. Vaginal mucormycosis: a case report. Infect Dis Obstet Gynecol. 2001;9(2):117–118. doi: 10.1155/S1064744901000205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Sobel J. D., Vazquez J., Lynch M., Meriwether C., Zervos M. J. Vaginitis due to Saccharomyces cerevisiae: epidemiology, clinical aspects, and therapy. Clin Infect Dis. 1993 Jan;16(1):93–99. doi: 10.1093/clinids/16.1.93. [DOI] [PubMed] [Google Scholar]
  11. Thérizol-Ferly M., Kombila M., Gomez de Diaz M., Duong T. H., Richard-Lenoble D. White piedra and Trichosporon species in equatorial Africa. I. History and clinical aspects: an analysis of 449 superficial inguinal specimens. Mycoses. 1994 Jul-Aug;37(7-8):249–253. doi: 10.1111/j.1439-0507.1994.tb00421.x. [DOI] [PubMed] [Google Scholar]

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