Abstract

The goal of this study was to review 18 cases of phaeohyphomycosis in Rio Grande do Sul. The records of all of the patients with a diagnosis of phaeohyphomycosis between 1995-2010 were reviewed. Twelve of the 18 patients (66.6%) were male. The average age of the patients was 50 years old (range: 16-74 years). Eleven patients (61%) presented with subcutaneous lesions. Seven patients (38.8%) had received a solid organ transplant. In all of the cases, the presence of melanin in the fungal cells was determined by Fontana-Masson staining of tissue sections and documented. Among the 18 patients, a total of 11 different fungal species were isolated. The causative organisms included Exophiala jeanselmei, Alternaria, Curvularia, Cladophialophora and Colletotrichum gloeosporioides. To our knowledge, this review reports the first case of subcutaneous phaeohyphomycosis caused by C. gloeosporioides in a lung transplant patient. The number of reported cases of phaeohyphomycosis has increased in the last decade. In a number of cases, this increased incidence may be primarily attributed to iatrogenic immunodeficiency.

Highlights

  • The goal of this study was to review 18 cases of phaeohyphomycosis in Rio Grande do Sul

  • Phaeohyphomycosis can be distinguished from two other subcutaneous mycoses caused by phaeoid fungi: Chromoblastomycosis and Mycetoma

  • We retrospectively reviewed the clinical data, epidemiological data and diagnoses of 18 cases of phaeohyphomycosis identified between 1995-2010 by the Mycology Laboratory of the Santa Casa Medical Centre, Porto Alegre, Rio Grande do Sul (RS), Brazil

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Summary

Introduction

The goal of this study was to review 18 cases of phaeohyphomycosis in Rio Grande do Sul. This review reports the first case of subcutaneous phaeohyphomycosis caused by C. gloeosporioides in a lung transplant patient. The term phaeohyphomycosis (from the Greek phaios, meaning dark or darkish) was introduced by Ajello et al in 1974 to designate infections by phaeoid or pigmented filamentous fungi that contain melanin in their walls. The diagnosis is necessarily supported by the examination of cultures to identify the genus and species of the aetiological agent (Lacaz et al 2002) The rarity of this mycosis justifies describing the clinical, epidemiological and diagnostic characteristics to aid in its immediate recognition and early treatment. We retrospectively reviewed the clinical data, epidemiological data and diagnoses of 18 cases of phaeohyphomycosis identified between 1995-2010 by the Mycology Laboratory of the Santa Casa Medical Centre, Porto Alegre, Rio Grande do Sul (RS), Brazil. The study was approved by the Committee of Research and Ethical of Santa Casa Medical Centre (protocol 3098/89)

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