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Neoscytalidium Dimidiatum As Onychomycosis Causative Agent in an Iranian Patient: A Case Report and Literature Review Publisher



Razavyoon T1 ; Hashemi SJ1 ; Ansari S2 ; Mansouri P3 ; Daieghazvini R1 ; Khodavaisy S1 ; Rafat Z4 ; Kamali Sarvestani H1 ; Hosseinpour L1 ; Afshar P5 ; Hashemi F6 ; Safaie F7
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Skin and Stem Cell Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Medical Microbiology, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
  5. 5. Research and Development of Referral Laboratory, Deputy of Health Management, Mazandaran University of Medical Sciences, Sari, Iran
  6. 6. School of Pharmacy, Tehran University of Medical Sciences, Iran
  7. 7. Islamic Azad University, Tehran Medical Branch, Iran

Source: New Microbes and New Infections Published:2022


Abstract

A 38-year-old healthy male presented to our medical mycology center with whitish opaque discoloration of the right toenail. He reported a history of some sand scratches subsequent to walking barefoot on the beach two years ago and wearing hard safety shoes for a period of two years. On clinical examination, onycholysis, onychodystrophy, and apparent thickening of the ungual bed in the left big toe were found. The microscopic examination of nail clippings using 15% potassium hydroxide (KOH/) revealed the presence of septate pigmented hyphae. The fungus was identified as Neoscytalidium dimidiatum based on the cultural characteristics, the arrangement of arthroconidia on lactophenol cotton blue (LPCB) staining, blocky-brown pigmented hyphae on serum physiology mounts, and sequencing. Susceptibility of the isolated fungi to amphotericin B, itraconazole, voriconazole, and terbinafine was tested using the standard broth microdilution M38-A2 method developed by the Clinical and Laboratory Standards Institute (CLSI). The minimum inhibitory concentrations (MICs) of the four antifungal drugs used in this study were: amphotericin B: 1 mg/L, itraconazole: 2 mg/L, voriconazole: 0.25 mg/L, and terbinafine: 1 mg/L. The patient underwent terbinafine and clobetasol topical treatments for 6 months. © 2022