Literature DB >> 33098693

'Mask tinea': tinea faciei possibly potentiated by prolonged mask usage during the COVID-19 pandemic.

A Agarwal1, T Hassanandani1, A Das2, M Panda1, S Chakravorty3.   

Abstract

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Year:  2020        PMID: 33098693      PMCID: PMC9213933          DOI: 10.1111/ced.14491

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN: 0307-6938            Impact factor:   4.481


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The COVID‐19 pandemic emerged when India was already facing an epidemic‐like situation of superficial dermatophytosis (tinea). The prevalence of tinea in India is currently 27.6%, with tinea faciei accounting for 1.8% cases. The use of face masks, although necessary, has the potential to aggravate a worrisome situation with regard to tinea in India. We report seven nonfamilial cases of tinea faciei (confirmed by culture and potassium hydroxide staining) all of which involved the facial area covered by a mask (Fig. 1, Fig. 2, Table 1). The lesions appeared after the patients began using masks. Mean duration of mask use was 6–7 h/day. Patients reused masks without daily washing (mean duration 6–7 days before washing), and the used masks were often stored and washed with other clothing. Five patients had pre‐existing plaques of tinea (tinea corporis, cruris and unguium) elsewhere. Presence of tinea infections among family members was noted in four patients, three of whom gave a history of sharing masks with other family members. Three patients had pre‐existing diabetes mellitus. All the patients were treated with oral and topical antifungals, and given advice regarding proper mask use.
Figure 1

(a,b) Tinea faciei presenting as (a) a serpiginous plaque localized above left nasolabial fold in Patient1 and (b) as scaly plaque with a defined margin seen in the neck region in Patient 2. (c) Lactophenol cotton blue mount showing tear‐drop microconidia consistent with Trichophyton rubrumin a culture from Patient 1.

Figure 2

(a,b) Tinea faciei as (a) an annular plaque 30 × 30 mm in size on the right cheek in Patient 3 (b) and (b) as an erythematous annular plaque localized to the leftcheek of Patient 4. (c) Lactophenol cotton blue mount showing spiral hyphae consistent with Trichophyton mentagrophytesin a culture from Patient 3.

Table 1

Characteristics of patients presenting with ‘mask tinea’.

PatientAge, years/sexFungal cultureLocation of tinea on faceMean duration of mask use per day, hTinea lesions elsewhere in the bodyMean duration between washing masks, daysFamily history of tineaSharing of mask among family membersConcurrent disease/medication
150/M Trichophyton rubrum Above left nasolabial fold8–10Tinea corporis, cruris and unguium (toe)7YesNoType 2 DM, uncontrolled/insulin
235/F T. rubrum Neck region6No7YesYesType 2 DM, controlled/metformin
330/M Trichophyton mentagrophytes Right cheek8Tinea cruris3–4NoNo
440/F T. mentagrophytes Left cheek6–8No5YesYesType 2 DM, controlled/metformin
525/M T. mentagrophytes Left cheek8–10Tinea cruris, corporis and unguium (finger)5–7YesYes
643/M T. rubrum Right cheek6–8Tinea cruris10NoNo
718/F T. mentagrophytes Right cheek6Tinea cruris7NoNo
(a,b) Tinea faciei presenting as (a) a serpiginous plaque localized above left nasolabial fold in Patient1 and (b) as scaly plaque with a defined margin seen in the neck region in Patient 2. (c) Lactophenol cotton blue mount showing tear‐drop microconidia consistent with Trichophyton rubrumin a culture from Patient 1. (a,b) Tinea faciei as (a) an annular plaque 30 × 30 mm in size on the right cheek in Patient 3 (b) and (b) as an erythematous annular plaque localized to the leftcheek of Patient 4. (c) Lactophenol cotton blue mount showing spiral hyphae consistent with Trichophyton mentagrophytesin a culture from Patient 3. Characteristics of patients presenting with ‘mask tinea’. Face masks create a humid microenvironment due to occlusion and increased sweating, which are the perfect conditions for the fungus. In a tropical country such as India where the burden of tinea is already high, we believe that the widespread promotion and use of cloth face masks is acting as a source for the inoculation and spread of dermatophytes., In all patients, the source of infection was either from a coexisting area of tinea elsewhere or from an infected family member. Most of the patients reused and shared masks, and washed masks along with their regular clothing. Hammer et al. found that 10% of infectious material was transferred from contaminated to sterile textiles during common storage, and 16% of spores were transferred during washing of clothes in the same vessel. Washing of contaminated clothes at 60 °C is recommended to eliminate fungal pathogens, which is not commonly practised in India. This explains how the fungus spreads from clothes to the mask, and persists even after regular washing. Family history of tinea, fomite spread, tight clothing, hot and humid climate, and pre‐existing diabetes are documented risk factors for acquiring tinea (noted in our patients). Multiple lockdowns impinging access to healthcare, along with personal neglect and use of over‐the‐counter treatments could also be precipitating factors. We propose calling this new variant of tinea faciei, ‘mask tinea’, owing to its peculiar location, associated cosmetic blemishes and difficulty in prevention. The masking effect due to the protective face covers could lead to a delay in diagnosis, thus we advocate thorough examination of the mask area in patients with tinea. A limitation of our case series is that we cannot confidently attribute this type of tinea solely to the wearing of masks, as other proven risk factors should be considered as well. Establishing the causality requires further case−control studies. As dermatologists, we should be aware about this increasing problem due to the novel mask requirements by the general public during the COVID‐19 pandemic. Consequently, proper counselling regarding use, handling and sanitization of the ubiquitous mask should also be done.
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