Response of chromoblastomycosis to voriconazole^*

Abstract:

Chromoblastomycosis is a chronic fungal infection of the epidermis, dermis and subcutaneous tissue, in which the most common etiologic agent in Brazil is Fonsecaea pedrosoi. In more advanced cases we found many difficulties in their treatment, and therefore, we report a case of extensive and severe chromoblastomycosis, with therapeutical failure of first choice treatments, but good response to voriconazole.

Keywords:
Antifungal agents; Chromoblastomycosis; Fungi

Male, Caucasian, 48 years old, rural worker, after an accident with a tree branch, for the last five years has had onset of pruritus and nodular lesion on the lower left limb and lumbar region, evolving to progressive increase in erythematous verrucous plaques with areas of atrophy (Figure 1). It was then diagnosed as chromoblastomycosis by Fonsecaea pedrosoi. Since the diagnosis, during these five years the patient has undergone many treatments such as: cryosurgery; stand alone itraconazole or in combination with thermotherapy; cryosurgery and terbinafine; and itraconazole associated with terbinafine, all of them not providing apparent clinical response. In his last medical visit, patient was hospitalized and received voriconazole 200mg every 12 hours and, in four weeks of treatment, a significant improvement of lesions was observed, recovering movement of left knee (Figures 2, 3 and 4).

Figure 1
Verrucous plaques with meliceric-hematic crusts on the buttock and left lower limb

Figure 2
Weekly clinical evolution of verrucous lesions during 30 days of hospitalization

Figure 3
Acute flattening of verrucous plaques after 12 months of treatment with voriconazole (200mg orally every 12 hours).

Figure 4
Marked improvement of verrucous lesions after 12 months of treatment (side view)

DISCUSSION

Voriconazole, a new second-generation triazole, which has been effective in cases of cerebral and disseminated phaeohyphomycosis, demonstrated activity in vitro against the main etiological agents of chromoblastomycosis, such as Fonsecaea pedrosoi, Fonsecaea monophora, Fonsecaea nubica and Cladophialophora carrionii.^1,4 Similar to voriconazole, posaconazole and isavuconazole seem to be potential candidates for use in treatment of chromoblastomycosis, for they present the lowest minimal inhibitory concentrations in studies with specimens of Fonsecaea. However, only posaconazole is commercially available in Brazil since 2015.^2,5 It is important to highlight the improvement of clinical conditions and quality of life of these patients, who are resistant to conventional therapeutics, with these new medications. However, clinical suspicion and early therapy in initial cases are still paramount for therapeutic success.

• Financial Support: None
• *
  Work performed at Hospital Universitário Maria Aparecida Pedrossian -Universidade Federal de Mato Grosso do Sul (HUMAP-UFMS) – Campo Grande (MS), Brazil.

REFERENCES

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• ²
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  Criado PR, Valente NY, Brandt HR, Belda Junior W, Halpern I. Dermatite verrucosa de Pedroso e Gomes (Cromomicose): 90 anos depois, ainda entre nós. An Bras Dermatol. 2010;85:104-5.
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  Najafzadeh MJ, Badali H, Illnait-Zaragozi MT, De Hoog GS, Meis JF. In vitro activities of eight antifungal drugs against 55 clinical isolates of Fonsecaea spp. Antimicrob Agents Chemother. 2010;54:1636-8.

Publication Dates

• Publication in this collection
  Sep-Oct 2016

History

• Received
  15 Sept 2015
• Accepted
  16 Nov 2015