Annals of Clinical Microbiology, The official Journal of the Korean Society of Clinical Microbiology

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Review article

Prevalence, clinical features, and diagnostic methods of dermatophyte skin infection in Korea

Department of Dermatology, College of Medicine, The Catholic University of Korea, Seoul, Korea

Corresponding to Young Bok Lee, E-mail: lyb80@catholic.ac.kr

Ann Clin Microbiol 2025;28(1):1. https://doi.org/10.5145/ACM.2025.28.1.1
Received on 9 October 2024, Revised on 28 November 2024, Accepted on 29 November 2024, Published on 30 December 2024.
Copyright © Korean Society of Clinical Microbiology.
This is an Open Access article which is freely available under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/).

Abstract

Cutaneous dermatophyte infections, dermatophytosis, are common worldwide, affecting various age groups and body parts. Despite advancements in antifungal therapies, the prevalence of dermatophytosis continues to increase, posing significant challenges for diagnosis and treatment. This review provides an overview of the prevalence, clinical features, and diagnostic methods for dermatophytosis in Korea. A comprehensive review of domestic reports and research on dermatophytosis in Korea was conducted using data from KoreaMed. This study covers the various clinical presentations, age distributions, seasonal trends, and types of dermatophytes identified in different body areas. Dermatophytosis in Korea have shown changing patterns in terms of prevalence and causative species. Trichophyton rubrum remains the most common causative organism, with varying presentations depending on the site of infection, such as tinea pedis, tinea corporis, tinea capitis, tinea faciei, and onychomycosis. Diagnostic practices largely depend on the potassium hydroxide smear test, which has limited sensitivity, particularly for onychomycosis. Recent trends indicate an increase in the incidence of dermatophytosis among older adults, which may be linked to underlying health conditions and lifestyle changes. Dermatophytosis in Korea exhibit diverse clinical manifestations influenced by factors such as patient age, body site, and seasonal variation. Improved diagnostic methods are needed to enhance the accuracy and guide appropriate treatment, especially with the emergence of antifungal-resistant strains. This review aims to provide a better understanding of the current state of dermatophytosis in Korea and contribute to more effective management and prevention strategies.

Keywords

Dermatophytes, Dermatophytoses, Tinea, Korea

Introduction

Background

Fungal skin infections are generally classified as those caused by dermatophytes or non-dermatophyte fungi. Most cases are due to dermatophytes, and dermatophytoses that thrive during hot and humid seasons [1]. These infections affect a wide range of age groups, from infants to older adults, and can occur in various body parts, including the face, scalp, nails, trunk, and extremities [2]. Without proper management, these infections have a high recurrence rate and are highly contagious, leading many individuals to seek dermatological treatment [2].

Dermatophytoses have various clinical manifestations. Although dermatologists can often visually diagnose these infections based on their characteristic clinical features, diagnosis can be more challenging when patients receive other treatments, when atypical clinical features are present, or when visual diagnosis alone is difficult [3]. In such cases, laboratory tests are often required for diagnosis. Methods such as direct potassium hydroxide (KOH) examination in the clinic, biopsy, or fungal culture can be used to confirm the disease.

Objectives

This review summarizes domestic reports on dermatophytoses in Korea gathered through searches in KoreaMed. This study provides valuable insights into dermatophytoses in Korea, considering its unique geographical and climatic characteristics. This review aimed to provide a detailed examination of the prevalence, types, and identified fungal species of dermatophytoses in Korea.

Epidemiology of dermatophytosis

Global incidence of dermatophytosis

Dermatophytosis is a common disease worldwide, affecting an estimated 20%–25% of the global population [4]. Hot and humid climates significantly influence the prevalence of dermatophytoses. However, recently, various factors such as increased international travel and a rise in the immunocompromised and aging populations have contributed to changes in its prevalence [5,6].

Dermatophytosis occurs primarily in patients with poor hygiene or inadequate nutrition. Notably, despite improvements in living standards, hygiene, and nutritional status, the incidence of dermatophytosis has shown an upward trend [7]. This is associated with an increase in conditions that lead to diabetes or immunosuppression, the use of steroids, and a growing number of pets.

Recent epidemiological studies indicate that dermatophytosis is one of the most prevalent superficial fungal infections worldwide. In particular, drug-resistant dermatophytic strains have emerged that pose a significant challenge for effective management and treatment. This increase in resistance is partly attributable to the widespread use of over-the-counter antifungal medications and incomplete treatment courses. Furthermore, lifestyle changes such as the increased use of communal spaces (e.g., gyms and swimming pools), a growing preference for tight clothing, and the use of synthetic footwear have contributed to the persistence and spread of dermatophytoses. Consequently, dermatophytosis continues to be a public health concern, necessitating further research for improved prevention and treatment strategies.

Epidemiology of dermatophytosis in Korea

The causative fungi of cutaneous dermatophytosis in Korea have changed over time [812]. Several factors such as socioeconomic status, lifestyle, and the development of new antifungal drugs have contributed to changes in the main causative dermatophytes of superficial mycoses. With advancements in antifungal agents, an increasing number of patients have sought treatment at dermatological clinics for dermatophytosis, which is more commonly observed in men than in women.

According to a study conducted by a Korean research team, the number of patients with dermatophytosis is increasing annually [8]. Analysis of the causative strains in 1,314,400 patients revealed that the most common causative organism was Trichophyton rubrum (88.4%), followed by T. mentagrophytes, Microsporum canis, and Epidermophyton floccosum. Although infections caused by T. rubrum are increasing each year, the identification rates of T. mentagrophytes, M. canis, and E. floccosum have been decreasing [8]. In a study by Lee et al. [9] that analyzed patients suspected of having superficial mycoses at Asan Medical Center in Seoul from 1998 to 2002, the age distribution of dermatophytosis showed a normal distribution, peaking in the 40s and 50s for both men and women. The toenails, feet, fingernails, trunk, groin, scalp, and face were most commonly affected, in that order. The positivity rate for the KOH smear test was 49% and that for fungal cultures was 51%. The identified fungi included dermatophytes (78.5%), yeasts (20.5%), and nondermatophytic molds (1.0%) [9]. Among the dermatophytes, T. rubrum was the most prevalent, followed by Candida and Trichosporon species. Non-dermatophytic molds are primarily Aspergillus species [9]. Except for the scalp and face, T. rubrum was the dominant species across all body parts. On the scalp, M. canis was the most frequently found, whereas T. mentagrophytes was the most common on the face. Candida species were mainly detected on the fingernails, toenails, hands, and feet, with Candida parapsilosis being the most prevalent. Trichosporon species were found in about 8%–10% of cases, primarily on the feet, toenails, and hands. Non-dermatophytic molds are mostly detected on the fingernails and hands, accounting for 1.0% of the total identified fungi [9]. Another study by Lee et al. [10] analyzed 7,487 patients who visited the Dermatology Department of Chonnam National University Hospital and were clinically suspected of having superficial mycoses. The study concluded that patients with superficial mycoses accounted for 12.5% of all new patients. By age, 24.2% were in their 60s or older, and 17.7% were in their 50s; however, the disease was relatively evenly distributed across all age groups above 20 years. The male-to-female ratio was 1.2:1, indicating a higher prevalence among males. Seasonal distribution showed a peak in the summer months (June–August, 33.4%) [10]. The most common clinical type of tinea was tinea pedis (24.1%), followed by onychomycosis (18.1%), tinea corporis (14.5%), tinea cruris (9.3%), tinea faciale (7.7%), tinea manuum (7.5%), candidiasis (7.0%), pityriasis versicolor (6.3%), and tinea capitis (5.2%). Coinfections were observed in 693 patients (9.2%), with the most common being the co-occurrence of tinea pedis and onychomycosis. The positive rate of the KOH test was 49.7%, and the culture rate was 36.5% [10]. The frequency of isolated fungi in cases of superficial mycoses was as follows: T. rubrum (34.1%), C. albicans (9.6%), M. canis (5.4%), T. mentagrophytes (3.9%), M. gypseum (0.4%), E. f loccosum (0.3%), T. verrucosum (0.3%), T. tonsurans (0.1%), and T. violaceum (0.1%) [10]. According to Lee et al. [11], who analyzed the medical records of Kyungpook National University from 2013 to 2016, fungal infections most commonly occurred in patients in their 50s and peaked in August. The most common clinical type of superficial fungal infection is tinea pedis, and the most prevalent causative fungus is Trichophyton rubrum

According to a study conducted by a research team at Kyungpook University in Korea, the number of patients with dermatophytosis is increasing every year [8]. Analysis of the causative strains in 1,314,400 patients revealed that the most common causative organism was Trichophyton rubrum (88.4%), followed by T. mentagrophyte, Microsporum canis, and Epidermophyton floccosum. Although infections caused by T. rubrum are increasing annually, the identification rates of T. mentagrophyte, M. canis, and E. floccosum have been reported to be decreasing [8]. Moreover, these studies highlighted certain demographic trends, indicating that dermatophytosis is more prevalent in the elderly population, possibly because of the increased vulnerability associated with aging, immunosenescence, and chronic conditions such as diabetes. Geographic analysis within Korea has shown a higher incidence in urban areas, which is potentially linked to lifestyle factors such as the use of communal facilities and tight, non-breathable clothing [8].

The increase in T. rubrum infections is thought to be associated with its high adaptability to the keratinized environment of the human skin and its resistance to common antifungal treatments. Conversely, the decreases in T. mentagrophyte, M. canis, and E. floccosum may be owing to improved hygiene practices, reduced animal exposure, and changes in public health measures. These evolving patterns underscore the need for ongoing surveillance and tailored strategies for managing dermatophytosis in South Korea (Table 1).

Table 1. Comparative overview of dermatophytosis epidemiological studies in Korea

Studies Research Period Institution Sample Size Key Findings Key Demographics
[8] 1979–2013 Catholic Skin Clinic, Daegu 415,526 cases (131,440 confirmed) T. rubrum increasing; decline in E. floccosum. Higher incidence in urban areas; more common in males.
[9] 1998–2002 Asan Medical Center 8,955 patients T. rubrum most prevalent; KOH positivity 49.2%. Age peak: 40–50s; Male-to-female ratio: 1.09:1.
[10] 2001–2010 Chonnam National University 7,785 patients T. rubrum (51.1%), Candida spp. (33.2%) common. Common in older adults (60s); Male-to-female ratio: 1.2:1.
[11] 2013–2016 Kyungpook National University 20,413 patients (8,106 culture positive) Most common: Tinea pedis; causative agent: T. rubrum. Predominantly males; peak in 50s; seasonal peak in August.

Various dermatophytoses according to the body sites (Table 2)

Tinea pedis

Tinea pedis (athlete’s foot) is an extremely common condition, with global statistics indicating a prevalence of 20%–25% in the population. Despite the development of various antifungal agents, the prevalence has continued to rise over the years [4,13]. The prevalence of tinea pedis can change owing to factors such as migration to different regions, travel, host immunity, advancements in medical technology, and socioeconomic status. The increase in prevalence is believed to be due to factors such as an aging population, an increase in immunocompromised individuals resulting from the use of antibiotics and immunosuppressants, and the increased use of sports facilities such as swimming pools and gyms [6].

Recently, Cho et al. [14] analyzed the results of a public awareness and behavior survey on athlete’s foot conducted by the Korean Dermatological Association in 2022 in commemoration of the 20th Skin Health Day. Although tinea pedis is a well-known and common condition, this study reported that the public awareness of tinea pedis is insufficient. More than 25% of the individuals relied on self-diagnosis and the use of over-the-counter medications or home remedies. Some of these remedies include “soaking feet in vinegar or glacial acetic acid,” “soaking feet in soju or alcohol,” and “bursting blisters before applying medication [14].

This highlights the urgent need to raise awareness regarding the accurate diagnosis and appropriate treatment of tinea pedis.

Tinea pedis can be clinically classified into interdigital, vesicular, hyperkeratotic, and mixed types [15]. The interdigital type is the most common form of tinea pedis, characterized by maceration, fissures, or scaling of the skin in the interdigital spaces, most frequently affecting the fourth toe web, followed by the third toe web. This type has a high fungal positivity rate and can spread to the soles in warm and moist environments, potentially leading to secondary bacterial infections through the damaged skin. The hyperkeratotic type is the most common form of chronic fungal infection and presents with thickened keratin scaling across the entire sole. Patients typically present with minimal subjective symptoms. The vesicular type refers to vesicles scattered on the soles or sides of the feet. Upon infection, it triggers inflammation and blister formation, with heat and moisture playing important roles. The vesicles are often itchy during formation. These three types are often difficult to distinguish clearly, and multiple types frequently occur in a mixed form [15].

Tinea pedis thrives in hot and humid climates, and in Korea, it has a high military infection rate [16]. Soldiers live in close quarters in barracks and wear enclosed military boots even during hot and humid summers, which may have contributed to the high prevalence of tinea pedis. In the U.S. military, the prevalence rate is reported to be as high as 75% in summer [17], whereas in tropical regions such as Colombia, the prevalence among soldiers ranges from 64% to 84% [18]. According to a study by Seo et al. [16], the prevalence of tinea pedis in a Korean battalion was 51.5%, with the highest rate of 74% in August and the lowest rate of 36.7% in February. Among Korean soldiers, the interdigital type was the most common, observed in 60% of cases. The fungal strains identified were T. rubrum (67.7%) and T. mentagrophytes (25.8%) [16].

In another study by Park et al., the prevalence of tinea pedis in Korea was found to be the highest in patients aged 60 years and above (25.6%), followed by those in their 50s (23%), 40s (17.6%), 20s (10.8%), and teens (4.1%) [19]. The clinical manifestations observed were interdigital (50%), interdigital-hyperkeratotic (43.6%), and interdigital-vesicular (4%). Mycologically, T. rubrum was identified in 96% of cases, whereas T. mentagrophytes was observed in 4% of cases [19].

Tinea pedis frequently recurs and can spread to other parts of the body, thus serving as an important source of infection for tinea in others. It often spreads through keratin particles containing fungi shed from patient lesions, thereby increasing the likelihood of infection within the family.

 

Table 2. Summary of dermatophytic skin infections in Korea: key features, causative agents, and epidemiological insights

Dermatophytoses Clinical Characteristics Most Common Fungi Prevalence in Korea
Tinea pedis Common globally (20%-25%). Interdigital type most common. High prevalence in military personnel. Causes include aging, immunosuppression, and humid environments. T. rubrum, T. mentagrophytes 51.5% in Korean soldiers; 75% in U.S. military during summer.
Tinea corporis Occurs on non-hairy skin. Most common annular type in Korea (87.6%). Coinfections common, mainly with tinea pedis and onychomycosis. T. rubrum, T. mentagrophytes, M. canis Annular type most common (87.6%). Coinfections in 57.1% of cases.
Tinea capitis Occurs on scalp and hair follicles. More common in children. Increased incidence in adults due to immunosuppression. M. canis most common in children, T. rubrum in adults. M. canis (children), T. rubrum (adults) Primarily children (85.5% M. canis). Increasing cases in adults, especially postmenopausal women.
Onychomycosis Fungal infection of nails. Common in elderly. T. rubrum most frequent in toenails; Candida spp. in fingernails. Rising in children due to lifestyle changes. T. rubrum, Candida albicans Higher in elderly; rising in children. T. rubrum causes 76% of toenail infections in Korea.
Tinea faciei Occurs on hairless facial areas. Often misdiagnosed as dermatitis or rosacea. Common in agricultural workers. T. rubrum most prevalent. T. rubrum, T. mentagrophytes, T. tonsurans More frequent in men and agricultural workers. Cheeks most commonly affected (64.3%).
Tinea cruris Groin infection. Common in males. Often associated with tinea pedis. T. rubrum most frequent causative agent (93.5%). T. rubrum, T. mentagrophytes, E. floccosum Male-to-female ratio as high as 23.9:1. Peaks in summer.
Tinea manuum Affects hands, commonly linked to tinea pedis. “Two feet–one hand” syndrome common. T. rubrum most frequent cause. T. rubrum, T. mentagrophytes, M. gypseum Higher in men (Male:Female = 2:1). Frequently coexists with other tinea infections.

Abbreviations: GVHD, graft-versus-host disease; COVID-19, coronavirus disease 2019.

Tinea corporis

Tinea corporis is an inflammatory or non-inflammatory dermatophytic infection that occurs on the skin, excluding the scalp, face, hands, feet, and groins. A typical lesion presents with a well-defined border surrounded by papules or vesicles, whereas the center heals to show either a hyperpigmented patch covered with scales or a normal skin color. Although tinea corporis can occur regardless of the region or age, it is more prevalent in individuals with poor hygiene or nutritional status, and hot and humid environments play a significant role in its development. Clinical manifestations were classified into annular, eczematous, annular, plaque, herpetiform, kerion, and crusted types.

According to Jang et al. [20], 87.6% of tinea corporis cases in Korea present with the annular type, 9.5% with the eczematous annular type, and 2.9% with the plaque type. Most patients had a disease duration of less than one month (64.8%) [20]. The size of the lesions varied, with 14.3% of lesions smaller than 2 cm, 53.4% between 2 and 5 cm, 19.0% between 5 and 10 cm, and 13.3% larger than 10 cm. The lesions were more commonly located in the non-exposed areas (55.7%) than in the exposed areas (44.3%). Co-infections with other types of tinea were observed in 57.1% of the cases, with tinea pedis being the most common (42.5%), followed by onychomycosis (28.7%), tinea cruris (19.1%), tinea faciei (8.5%), tinea manuum (4.3%), and tinea capitis (1.1%) [20]. The causative fungi varied depending on the clinical presentation; T. mentagrophytes infections were commonly associated with the eczematous annular type, whereas T. rubrum infections frequently presented with lesions sized between 2 and 10 cm. Infections caused by M. canis typically result in smaller clinical lesions than those caused by other species [20].

Tinea capitis

Tinea capitis is a dermatophyte infection of the hair follicles and scalp. Tinea capitis can present in both noninflammatory and inflammatory forms with a variety of clinical manifestations, making it necessary to differentiate it from conditions such as seborrheic dermatitis, folliculitis, alopecia areata, trichotillomania, psoriasis, and syphilis. The non-inflammatory types of tinea capitis include diffuse scaling, grey patches, and black dots, whereas the inflammatory types include diffuse pustular forms and kerion [21]. The typical clinical presentation of tinea capitis is a well-defined patch of hair loss accompanied by scaling especially in children. However, in adults, tinea capitis tends to be smaller, show less severe hair loss, and present with atypical and diverse clinical features, making them prone to misdiagnosis. Tinea capitis primarily occurs in children aged 3–14 years, its incidence decreases after puberty, and is relatively rare in adults. This is explained by several factors, including the antifungal activity of fatty acids in postpubertal sebum, maturity of hair follicles, and changes in the immune system in adults, which help prevent fungal infections [22]. However, the prevalence of tinea capitis has changed recently, and its occurrence in adults is increasing owing to various factors, such as systemic diseases and the prolonged use of steroids or immunosuppressants [23,24]. In particular, postmenopausal women are more susceptible to tinea capitis than other adults because of hormonal changes that further reduce the secretion of sebum, which has antimicrobial properties [25]. 

The causative fungi in children are mostly zoophilic species such as Microsporum canis. However, in Korean adults, recent studies have reported an increasing prevalence of anthropophilic species such as Trichophyton rubrum, in addition to M. canis [26,27]. Nonetheless, with the growing number of households keeping pets as a hobby, the incidence of zoophilic species is also increasing [28]. 

Recently, Seong et al. [29] analyzed the mycological characteristics of 60 adults and 58 children diagnosed with tinea capitis over a past 24 years. Microsporum canis was the most common causative organism in adults (48.8%) and children (85.5%). However, in adults, an increasing number of infections caused by dermatophytes other than Microsporum was identified [29]. This trend is consistent with the findings of studies by Lee et al. and Jung et al., who reported a recent increase in Trichophyton rubrum infections in adult tinea capitis [27,30]. In domestic studies, adult tinea capitis was more prevalent in women, particularly postmenopausal women [29,30]. Treatment of tinea capitis includes oral medications such as itraconazole and terbinafine, as well as topical agents containing sertaconazole.

Onychomycosis

Onychomycosis is a very common fungal infection of the nails caused by dermatophytes, yeasts, and non-dermatophytic molds. Onychomycosis poses cosmetic issues and can cause functional impairment, making treatment necessary to reduce the risk of transmission. It is considered an age-related infectious disease because of its increasing incidence among the elderly population. This is believed to be due to the underlying conditions and circulatory disorders common in older adults, which lead to nail deformities and delayed nail growth, thereby increasing susceptibility to fungal infections [31]. Onychomycosis is relatively rare in children compared to that in adults because of their different environmental and physical conditions. However, with lifestyle changes, such as increased use of antibiotics and immunosuppressants, exposure to swimming pools and gyms, and wearing tight shoes, the prevalence of onychomycosis in children is gradually increasing [32]. 

The main causative agents of onychomycosis are dermatophytes, which include Trichophyton rubrum, T. mentagrophytes, and Epidermophyton floccosum. Yeast species include Candida albicans, C. parapsilosis, and C. tropicalis, while non-dermatophytic molds include Scopulariopsis brevicaulis, Aspergillus sp., Fusarium sp., and Acremonium sp. [33,34]. 

Onychomycosis is clinically classified using the Zaias and Baran classification into distal and lateral subungual onychomycosis, white superficial onychomycosis, proximal subungual onychomycosis, and total dystrophic onychomycosis [35,36]. 

Lim et al. [37] have identified the clinical features and causative organisms of onychomycosis in South Korea. For toenail onychomycosis, T. rubrum was the most common pathogen, followed by T. mentagrophytes. Among the yeasts, C. albicans was the most frequently observed, followed by C. parapsilosis and C. tropicalis. In contrast, in fingernail onychomycosis, yeast infections account for 48.2%, dermatophyte infections for 44.4%, and non-dermatophytic molds for 7.4%. 

The prevalence of pediatric onychomycosis has increased in Korea. According to Kim et al. [38], the number of pediatric onychomycosis patients has gradually increased, and factors such as trauma, family history, and underlying diseases are associated with the condition. Fingernail onychomycosis occurs at a younger age than toenail onychomycosis, with C. albicans identified in more than 50% of cases. In toenail onychomycosis, T. rubrum was the most common fungus, observed in 76% of cases [38].

Tinea faciei

Tinea faciei is a relatively uncommon dermatophytic infection that occurs in hairless areas of the face, specifically from the forehead (where hair does not grow) to the jawline [39]. Historically, tinea faciei was generally classified as tinea corporis, and some mycologists still include it in this category. In Korea, it was also reported as tinea corpora until the 1970s. However, following a report by Yim et al. [40] in 1982, it was classified as a separate condition owing to the unique anatomical and physiological characteristics of the facial area, which influence the features of the lesion and the conditions that need to be differentiated.

Similar to tinea infections in other areas, tinea faciei often presents as a central area of healed scaly patches surrounded by a ring of erythema. However, owing to the high exposure of the face to sunlight and the use of cosmetics, it can manifest in atypical forms such as patches, plaques, or blisters [41]. This atypical presentation can often be mistaken for other facial skin conditions, such as lupus erythematosus, rosacea, atopic dermatitis, or granuloma annulare, leading to misdiagnosis. In Korea, there have been reports of tinea faciei presenting with atypical clinical manifestations [42,43], including cases resembling eczema herpeticum [44], contact dermatitis [45], and rosacea [46].

A common issue is the frequent use of steroid preparations without definitive mycological diagnostic tests such as KOH smears, under the assumption that the condition is common dermatitis. This leads to further confusion in diagnosis. Tinea faciei can exhibit clinical patterns similar to those of other dermatoses, and its prevalence, distribution of fungal species, and clinical presentation may vary depending on the environmental and regional characteristics.

Kim et al. [47] analyzed 56 patients diagnosed with tinea faciei who visited Daegu Catholic University between 2013 and 2014. The highest incidence was observed in patients in their 50s and the occurrence rate was higher in men than in women. The most common occupations among the patients were agriculture and livestock (46.6%), with a higher frequency than other occupational groups [47]. The most frequently affected area was the cheek (64.3%), followed by the forehead, temples, and nose. The average lesion size was relatively large with a mean diameter of 9.6 cm [47]. The cultured strains included T. rubrum (79.2%), T. mentagrophytes (8.3%), T. tonsurans (8.3%), and T. verrucosum (4.2%) [47].

Tinea cruris

Tinea cruris is a superficial dermatophytic infection that occurs in the groin and is more common in adult males. It frequently affects individuals living in hot and humid regions, and obesity and mechanical friction from tight-fitting underwear are important contributing factors. The higher prevalence of tinea cruris in men is thought to be due to men wearing more enclosed clothing, the groin area being more enclosed due to the presence of the scrotum, and increased physical activity, which raises the humidity and temperature in the groin area due to sweating. 

Shin et al. [48] analyzed 598 cases of tinea cruris in patients over 13 years of age who visited Yeungnam University. The results showed that the highest number of cases occurred during the summer, particularly in July and August, with a male-to-female ratio of 23.9:1, indicating a significantly higher prevalence in males. Regarding the identified strains, T. rubrum accounted for 93.5% of the identified strains, followed by T. mentagrophytes, E. floccosum, and M. canis [48]. Tinea cruris is most commonly associated with tinea pedis (22.4%), followed by onychomycosis (6.7% of cases) [48]. In a study by Lim et al. [49], which analyzed 89 patients with tinea cruris between 2000 and 2005, the male-to-female ratio was 10.8:1, with most cases occurring in individuals in their 20s to 40s. Among these patients, 8.7% had concurrent T. pedis, suggesting that many patients initially present with T. pedis symptoms. In this study, T. rubrum was identified in 89.2% of cases, T. mentagrophytes in 7.2%, and E. floccosum in 3.6% [49].

Tinea manus

Tinea manuum is a dermatophytic infection that occurs on the hands and accounts for approximately 5% of all tinea infections [12]. The main causative fungi of tinea manuum in Korea are Trichophyton rubrum, T. mentagrophytes, and Microsporum canis, with T. rubrum responsible for 76% of the cases. Many of these cases are associated with concurrent tinea pedia [12]. The primary source of infection for tinea manuum is self-inoculation, which is usually caused by scratching the lesions of the tinea pedis with the hands [50].

Tinea manuum often occurs alongside tinea pedis, and when it involves one hand and both feet or toenails, it is referred to as the “two feet-one hand” syndrome [50]. However, there are other reported routes of infection, such as direct contact with pets such as hedgehogs, leading to tinea development exclusively on the hands that came into contact with the infected animal. This phenomenon has been documented both domestically and international literature [5153]. In cases of tinea manuum caused by zoophilic subtypes such as T. mentagrophytes, atypically severe inflammatory lesions such as pustular patches may appear localized in areas exposed to the animal [5154].

According to a study on tinea manus in Korea published by Ko et al. [55], the incidence of tinea manus was higher in men than in women (Male:Female = 2:1), and the presence of other tinea lesions was also more common in men. Clinically, the most frequent site is the palm, followed by cases involving both the palm and dorsum of the hand [55]. The most common clinical presentation was the hyperkeratotic type, appearing as scaly patches on the palm, followed by the vesicular and interdigital types [55]. Coexisting tinea infections were observed in 78% of patients, with tinea pedis and onychomycosis being the most common, although tinea corporis was also noted. Among the cultured strains, T. rubrum was the most frequently isolated, followed by T. mentagrophytes and M. gypseum [55].

Diagnosis of dermatophytic infections in dermatologic clinics

A KOH smear is commonly used as the primary diagnostic test because it is simple and provides rapid results. However, its accuracy depends on the examiner’s skill and experience and is less sensitive than other diagnostic methods. In particular, the positivity rate of KOH in onychomycosis was lower than that of KOH results from other sites. According to a study by Lee et al. [56], the sensitivity of the KOH smear ranges from 16.7% to 70.0%, depending on the number of months of training of dermatology residents.

When onychomycosis is suspected but both fungal culture and KOH smear results are negative, a pathological staining examination of the nail plate can be considered to improve diagnostic accuracy. This involves aseptically cutting the nail plate of a suspected patient, followed by staining with Grocott-Gomori methenamine silver or periodic acid-Schiff to confirm the presence of fungi. Meta-analyses have shown that this test has a sensitivity of 84% and a specificity of 89%, offering the highest accuracy as a single diagnostic test [57,58].

Conclusions

Dermatophytoses vary depending on the site of occurrence, patient age, and medication history. For an accurate diagnosis, it is important to identify the fungus from the lesion site easily and quickly. Despite many advancements in identifying fungi, most clinical diagnoses still rely on the KOH method, which is simple to perform but has low sensitivity. However, owing to improper diagnosis and medication misuse, the prevalence of dermatophytosis has not decreased, and many patients require treatment each year.

Recently, the emergence of strains resistant to major treatment drugs such as terbinafine, itraconazole, and f luconazole has become a concern abroad, raising alarms for the treatment of dermatophytic infections. For dermatologists, it is necessary to develop new diagnostic methods to ensure more accurate patient treatment, which may also help prevent the misuse of medications.

Ethics statement

This was not a human population study; therefore, approval by the institutional review board and informed consent were not required.

Conflicts of interest

No potential conflicts of interest relevant to this article were reported.

Funding

None.

Data availability

None.

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2. Chanyachailert P, Leeyaphan C, Bunyaratavej S. Cutaneous fungal infections caused by dermatophytes and non-dermatophytes: an updated comprehensive review of epidemiology, clinical presentations, and diagnostic testing. J Fungi 2023;9:669.
  

3. Zacharopoulou A, Tsiogka A, Tsimpidakis A, Lamia A, Koumaki D, Gregoriou S. Tinea incognito: challenges in diagnosis and management. J Clin Med 2024;13:3267.
  

4. Havlickova B, Czaika VA, Friedrich M. Epidemiological trends in skin mycoses worldwide. Mycoses 2008;51(Suppl 4):2-15.
 

5. Ali-Shtayeh MS, Yaish S, Jamous RM, Arda H, Husein EI. Updating the epidemiology of dermatophyte infections in Palestine with special reference to concomitant dermatophytosis. J Mycol Med 2015;25:116-22.
 

6. Foster KW, Ghannoum MA, Elewski BE. Epidemiologic surveillance of cutaneous fungal infection in the United States from 1999 to 2002. J Am Acad Dermatol 2004;50:748-52.
 

7. Lee WJ, Kim SL, Jang YH, Lee SJ, Kim DW, Bang YJ, et al. Increasing prevalence of Trichophyton rubrum identified through an analysis of 115,846 cases over the last 37 years. J Korean Med Sci 2015;30:639-43.
  

8. Kim SL, Lee KC, Jang YH, Lee SJ, Kim DW, Lee WJ, et al. The epidemiology of dermatophyte infection in Southeastern Korea (1979~2013). Ann Dermatol 2016;28:524-7.
  

9. Lee DK, Moon KC, Koh JK. Clinical and mycological studies on superficial fungal infection. Korean J Med Mycol 2006;11:54-63.

10. Lee YW, Yoon SJ, Lee JB, Kim SJ, Lee SC, Won YH. Clinical and mycological studies on dermatomycosis (2001-2010). Korean J Med Mycol 2013;18:30-8.

11. Lee WJ, Eun DH, Jang YH, Bang YJ, Jun JB. The incidences of dermatophytosis and cutaneous candidiasis infection in Southeastern Korea between 2013 and 2016. Korean J Med Mycol 2018;23:1-8.

12. Jang SJ and Ahn KJ. Superficial dermatomycosis and the causative agents in Korea. Korean J Med Mycol 2004;9:91-9.

13. Ward H, Parkes N, Smith C, Kluzek S, Pearson R. Consensus for the treatment of tinea pedis: a systematic review of randomised controlled trials. J Fungi 2022;8:351.
  

14. Cho M, Lee YW, Lee DH, Jeong KH, Kwon SH, Kim JE, et al. A survey on the perception and behavior regarding tinea pedis among Korean adults. Korean J Dermatol 2023;61:420-8.

15. Lee SK, Choi JS, Kim KH. A Clinical and mycological study of tinea pedis. Korean J Dermatol 1995;33:1029-37.

16. Seo KI, Kim JA, Lim JG, Eun HC, Youn JI. Prevalence of tinea pedis in Korean soldiers in a battalion. Korean J Dermatol 2000;38:1050-4.

17. Taplin D. Superficial mycoses. J Invest Dermatol 1976;67:177-81.
 

18. Aly R. Ecology and epidemiology of dermatophyte infections. J Am Acad Dermatol 1994;31:S21-5.
 

19. Park SH, Shin YM, Moon SK, Shin DH, Choi JS, Kim KH, et al. A clinical and mycological study of tinea pedis. Korean J Med Mycol 2006;11:123-31.

20. Jang SJ, Choe YB, Ahn KJ. A clinical and mycological study of tinea corporis. Korean J Dermatol 2004;42:166-72.

21. Higgins EM, Fuller LC, Smith CH. Guidelines for the management of tinea capitis. Br J Dermatol 2000;143:53-8.
 

22. Gianni C, Betti R, Perotta E, Crosti C. Tinea capitis in adults. Mycoses 1995;38:329-31.
 

23. He M, Zeng J, Mao Y, Zheng Y, Lian X, Chen H. Aetiological changes of tinea capitis in the Hubei area in 60 years: focus on adult tinea capitis. Mycoses 2021;64:1527-34.
 

24. Khosravi AR, Shokri H, Vahedi G. Factors in etiology and predisposition of adult tinea capitis and review of published literature. Mycopathologia 2016;181:371-8.
 

25. Liang G, Zheng X, Song G, Zhang M, Liu J, Zang X, et al. Adult tinea capitis in China: a retrospective analysis from 2000 to 2019. Mycoses 2020;63:876-88.
 

26. Park SK, Park SW, Yun SK, Kim HU, Park J. Tinea capitis in adults: a 18-year retrospective, single-centre study in Korea. Mycoses 2019;62:609-16.
 

27. Lee HJ, Kim JY, Park KD, Jang YH, Lee SJ, Bang YJ, et al. Analysis of adult patients with tinea capitis in Southeastern Korea. Ann Dermatol 2020;32:109-14.
  

28. Lee YW, Lim SH, Yim SM, Choe YB, Ahn KJ. A clinical and mycological study of dermatophytosis associated with animal contact. Korean J Med Mycol 2005;10:151-9.

29. Seong M, Son H, Suh MK, Lee K. Clinical and mycological analysis of tinea capitis in adults and children during the last 24-year-period (1999~2022): a single-center study. Korean J Dermatol 2024;62:82-91.

30. Jung IS, Ryu GW, Yun SJ, Lee JB, Kim SJ, Lee SC, et al. Clinical and mycological features of tinea capitis in Korea: analysis of 61 cases from 1990 to 2018. Korean J Dermatol 2020;58:16.

31. Rodriguez-Pazos L, Pereiro-Ferreirós MM, Pereiro M Jr, Toribio J. Onychomycosis observed in children over a 20-year period. Mycoses 2011;54:450-3.
 

32. Lange M, Roszkiewicz J, Szczerkowska-Dobosz A, Jasiel-Walikowska E, Bykowska B. Onychomycosis is no longer a rare finding in children. Mycoses 2006;49:55-9.
 

33. Ghannoum MA, Hajjeh RA, Scher R, Konnikov N, Gupta AK, Summerbell R, et al. A large-scale North American study of fungal isolates from nails: the frequency of onychomycosis, fungal distribution, and antifungal susceptibility patterns. J Am Acad Dermatol 2000;43:641-8.
 

34. Gupta AK, Jain HC, Lynde CW, Macdonald P, Cooper EA, Summerbell RC. Prevalence and epidemiology of onychomycosis in patients visiting physicians’ offices: a multicenter Canadian survey of 15,000 patients. J Am Acad Dermatol 2000;43:244-8.
 

35. Zaias N. Onychomycosis. Arch Dermatol 1972;105:263-74.
 

36. Baran R and Hay RJ. New clinical classification for onychomycoses. J Mycol Med 2014;24:247-60.
 

37. Lim SW, Suh MK, Ha GY. Clinical features and identification of etiologic agents in onychomycosis (1999-2002). Korean J Dermatol 2004;42:53-60.

38. Kim NH, Yun SJ, Lee JB, Kim SJ, Lee SC, Won YH. Clinical study of onychomycosis observed in children (2005~2014). Korean J Dermatol 2016;54:781-7.

39. Drake LA, Dinehart SM, Farmer ER, Goltz RW, Graham GF, Hardinsky MK, et al. Guidelines of care for superficial mycotic infections of the skin: tinea corporis, tinea cruris, tinea faciei, tinea manuum, and tinea pedis. J Am Acad Dermatol 1996;34:282-6.
 

40. Yim SM, Choi YB, Ahn KJ. A clinical and mycological study of tinea faciale. Korean J Med Mycol 2004;9:214-21.

41. Noguchi H, Jinnin M, Miyata K, Hiruma M, Ihn H. Clinical features of 80 cases of tinea faciei treated at a rural clinic in Japan. Drug Discov Ther 2014;8:245-8.
 

42. Hur W, Koo SW, Hann SK, Bang D. Two cases of tinea faciei with atypical clinical manifestation. Korean J Dermatol 1991;29:414-8.

43. Park SB, Lee YW, Park EJ, Kwon IH, Kim KH, Kim KJ. A case of tinea faciei caused by Trichophyton mentagrophytes with atypical presentation. Korean J Med Mycol 2010;15:170-4.

44. Hwang J, Kang JM, Ahn JG. Two cases of tinea faciei mimicking eczema herpeticum in siblings. Pediatr Infect Vaccine 2021;28:49-56.

45. Kim WJ, Park JW, Shin DH, Choi JS, Kim KH. Three cases of tinea faciei misdiagnosed as contact dermatitis. Korean J Med Mycol 2004;9:54-9.

46. Kang GS, Hwang SM, Suh MK, Ha GY, Jang TJ. A case of rosacea-like tinea faciei caused by Trichophyton rubrum. Korean J Med Mycol 2010;15:22-6.

47. Kim I, Bang YJ, Jun JB, Park KD, Chung H, Park J. The clinical and mycological study of tinea faciei in Daegu. Korean J Med Mycol 2015;20:63-9.

48. Shin DH and Kim KH. Clinical and mycologic studies of tinea cruris. Korean J Dermatol 1999;37:219-24.

49. Lim JW, Suh MK, Ha GY. The frequency of tinea pedis in patients with tinea cruris. Korean J Med Mycol 2007;12:1-8.

50. Daniel CR 3rd, Gupta AK, Daniel MP, Daniel CM. Two feet-one hand syndrome: a retrospective multicenter survey. Int J Dermatol 1997;36:658-60.
 

51. Mochizuki T, Takeda K, Nakagawa M, Kawasaki M, Tanabe H, Ishizaki H. The first isolation in Japan of Trichophyton mentagrophytes var. erinacei causing tinea manuum. Int J Dermatol 2005;44:765-8.
 

52. Rhee DY, Kim MS, Chang SE, Lee MW, Choi JH, Moon KC, et al. A case of tinea manuum caused by Trichophyton mentagrophytes var. erinacei: the first isolation in Korea. Mycoses 2009;52:287-90.
 

53. Lim JH, Kim HS, Kim HO, Cho BK, Kim SI, Choi JS, et al. Tinea manus caused by Trichophyton mentagrophytes var. erinacei transferred from a hedgehog. Korean J Dermatol 2009;47:504-7.

54. Lee S and Ahn HJ. Pustular tinea manuum in a child caused by Trichophyton erinacei from a pet hedgehog. Korean J Dermatol 2023;61:204-6.

55. Ko D, Kim I, Chae I, Park KD, Chung H, Bang YJ, et al. The clinical and mycological study of tinea manus and concomitant dermatophytosis. Korean J Med Mycol 2013;18:102-10.

56. Lee JH, Kang JW, Nam MW, Lee JS. Investigating the diagnostic utility of potassium hydroxide (KOH) smear test and the influence of clinical and practical factors in onychomycosis. Korean J Dermatol 2024;62:228-33.

57. Baek G, Koo T, Lee D, Kang HJ, Kim MS, Kim Y, et al. Histopathological examination of the nail plate and comparison between periodic acid-schiff and gomori’s methenamine silver stains for the diagnosis of onychomycosis. Korean J Dermatol 2021;59:618-23.

58. Jung MY, Shim JH, Lee JH, Lee JH, Yang JM, Lee DY, et al. Comparison of diagnostic methods for onychomycosis, and proposal of a diagnostic algorithm. Clin Exp Dermatol 2015;40:479-84.
 

Table 1
Table 2

1. Segal E and Elad D. Human and zoonotic dermatophytoses: epidemiological aspects. Front Microbiol 2021;12:713532.

2. Chanyachailert P, Leeyaphan C, Bunyaratavej S. Cutaneous fungal infections caused by dermatophytes and non-dermatophytes: an updated comprehensive review of epidemiology, clinical presentations, and diagnostic testing. J Fungi 2023;9:669.

3. Zacharopoulou A, Tsiogka A, Tsimpidakis A, Lamia A, Koumaki D, Gregoriou S. Tinea incognito: challenges in diagnosis and management. J Clin Med 2024;13:3267.

4. Havlickova B, Czaika VA, Friedrich M. Epidemiological trends in skin mycoses worldwide. Mycoses 2008;51(Suppl 4):2-15.

5. Ali-Shtayeh MS, Yaish S, Jamous RM, Arda H, Husein EI. Updating the epidemiology of dermatophyte infections in Palestine with special reference to concomitant dermatophytosis. J Mycol Med 2015;25:116-22.

6. Foster KW, Ghannoum MA, Elewski BE. Epidemiologic surveillance of cutaneous fungal infection in the United States from 1999 to 2002. J Am Acad Dermatol 2004;50:748-52.

7. Lee WJ, Kim SL, Jang YH, Lee SJ, Kim DW, Bang YJ, et al. Increasing prevalence of Trichophyton rubrum identified through an analysis of 115,846 cases over the last 37 years. J Korean Med Sci 2015;30:639-43.

8. Kim SL, Lee KC, Jang YH, Lee SJ, Kim DW, Lee WJ, et al. The epidemiology of dermatophyte infection in Southeastern Korea (1979~2013). Ann Dermatol 2016;28:524-7.

9. Lee DK, Moon KC, Koh JK. Clinical and mycological studies on superficial fungal infection. Korean J Med Mycol 2006;11:54-63.

10. Lee YW, Yoon SJ, Lee JB, Kim SJ, Lee SC, Won YH. Clinical and mycological studies on dermatomycosis (2001-2010). Korean J Med Mycol 2013;18:30-8.

11. Lee WJ, Eun DH, Jang YH, Bang YJ, Jun JB. The incidences of dermatophytosis and cutaneous candidiasis infection in Southeastern Korea between 2013 and 2016. Korean J Med Mycol 2018;23:1-8.

12. Jang SJ and Ahn KJ. Superficial dermatomycosis and the causative agents in Korea. Korean J Med Mycol 2004;9:91-9.

13. Ward H, Parkes N, Smith C, Kluzek S, Pearson R. Consensus for the treatment of tinea pedis: a systematic review of randomised controlled trials. J Fungi 2022;8:351.

14. Cho M, Lee YW, Lee DH, Jeong KH, Kwon SH, Kim JE, et al. A survey on the perception and behavior regarding tinea pedis among Korean adults. Korean J Dermatol 2023;61:420-8.

15. Lee SK, Choi JS, Kim KH. A Clinical and mycological study of tinea pedis. Korean J Dermatol 1995;33:1029-37.

16. Seo KI, Kim JA, Lim JG, Eun HC, Youn JI. Prevalence of tinea pedis in Korean soldiers in a battalion. Korean J Dermatol 2000;38:1050-4.

17. Taplin D. Superficial mycoses. J Invest Dermatol 1976;67:177-81.

18. Aly R. Ecology and epidemiology of dermatophyte infections. J Am Acad Dermatol 1994;31:S21-5.

19. Park SH, Shin YM, Moon SK, Shin DH, Choi JS, Kim KH, et al. A clinical and mycological study of tinea pedis. Korean J Med Mycol 2006;11:123-31.

20. Jang SJ, Choe YB, Ahn KJ. A clinical and mycological study of tinea corporis. Korean J Dermatol 2004;42:166-72.

21. Higgins EM, Fuller LC, Smith CH. Guidelines for the management of tinea capitis. Br J Dermatol 2000;143:53-8.

22. Gianni C, Betti R, Perotta E, Crosti C. Tinea capitis in adults. Mycoses 1995;38:329-31.

23. He M, Zeng J, Mao Y, Zheng Y, Lian X, Chen H. Aetiological changes of tinea capitis in the Hubei area in 60 years: focus on adult tinea capitis. Mycoses 2021;64:1527-34.

24. Khosravi AR, Shokri H, Vahedi G. Factors in etiology and predisposition of adult tinea capitis and review of published literature. Mycopathologia 2016;181:371-8.

25. Liang G, Zheng X, Song G, Zhang M, Liu J, Zang X, et al. Adult tinea capitis in China: a retrospective analysis from 2000 to 2019. Mycoses 2020;63:876-88.

26. Park SK, Park SW, Yun SK, Kim HU, Park J. Tinea capitis in adults: a 18-year retrospective, single-centre study in Korea. Mycoses 2019;62:609-16.

27. Lee HJ, Kim JY, Park KD, Jang YH, Lee SJ, Bang YJ, et al. Analysis of adult patients with tinea capitis in Southeastern Korea. Ann Dermatol 2020;32:109-14.

28. Lee YW, Lim SH, Yim SM, Choe YB, Ahn KJ. A clinical and mycological study of dermatophytosis associated with animal contact. Korean J Med Mycol 2005;10:151-9.

29. Seong M, Son H, Suh MK, Lee K. Clinical and mycological analysis of tinea capitis in adults and children during the last 24-year-period (1999~2022): a single-center study. Korean J Dermatol 2024;62:82-91.

30. Jung IS, Ryu GW, Yun SJ, Lee JB, Kim SJ, Lee SC, et al. Clinical and mycological features of tinea capitis in Korea: analysis of 61 cases from 1990 to 2018. Korean J Dermatol 2020;58:16.

31. Rodriguez-Pazos L, Pereiro-Ferreirós MM, Pereiro M Jr, Toribio J. Onychomycosis observed in children over a 20-year period. Mycoses 2011;54:450-3.

32. Lange M, Roszkiewicz J, Szczerkowska-Dobosz A, Jasiel-Walikowska E, Bykowska B. Onychomycosis is no longer a rare finding in children. Mycoses 2006;49:55-9.

33. Ghannoum MA, Hajjeh RA, Scher R, Konnikov N, Gupta AK, Summerbell R, et al. A largescale North American study of fungal isolates from nails: the frequency of onychomycosis, fungal distribution, and antifungal susceptibility patterns. J Am Acad Dermatol 2000;43:641-8.

34. Gupta AK, Jain HC, Lynde CW, Macdonald P, Cooper EA, Summerbell RC. Prevalence and epidemiology of onychomycosis in patients visiting physicians’ offices: a multicenter canadian survey of 15,000 patients. J Am Acad Dermatol 2000;43:244-8.

35. Zaias N. Onychomycosis. Arch Dermatol 1972;105:263-74.

36. Baran R and Hay RJ. New clinical classification for onychomycoses. J Mycol Med 2014;24:247-60.

37. Lim SW, Suh MK, Ha GY. Clinical features and identification of etiologic agents in onychomycosis (1999-2002). Korean J Dermatol 2004;42:53-60.

38. Kim NH, Yun SJ, Lee JB, Kim SJ, Lee SC, Won YH. Clinical study of onychomycosis observed in children (2005~2014). Korean J Dermatol 2016;54:781-7.

39. Drake LA, Dinehart SM, Farmer ER, Goltz RW, Graham GF, Hardinsky MK, et al. Guidelines of care for superficial mycotic infections of the skin: tinea corporis, tinea cruris, tinea faciei, tinea manuum, and tinea pedis. Guidelines/Outcomes Committee. American Academy of Dermatology. J Am Acad Dermatol 1996;34:282-6.

40. Yim SM, Choi YB, Ahn KJ. A clinical and mycological study of tinea faciale. Korean J Med Mycol 2004;9:214-21.

41. Noguchi H, Jinnin M, Miyata K, Hiruma M, Ihn H. Clinical features of 80 cases of tinea faciei treated at a rural clinic in Japan. Drug Discov Ther 2014;8:245-8.

42. Hur W, Koo SW, Hann SK, Bang D. Two cases of tinea faciei with atypical clinical manifestation. Korean J Dermatol 1991;29:414-8.

43. Park SB, Lee YW, Park EJ, Kwon IH, Kim KH, Kim KJ. A case of tinea faciei caused by Trichophyton mentagrophytes with atypical presentation. Korean J Med Mycol 2010;15:170-4.

44. Hwang J, Kang JM, Ahn JG. Two cases of tinea faciei mimicking eczema herpeticum in siblings. Pediatr Infect Vaccine 2021;28:49-56.

45. Kim WJ, Park JW, Shin DH, Choi JS, Kim KH. Three cases of tinea faciei misdiagnosed as contact dermatitis. Korean J Med Mycol 2004;9:54-9.

46. Kang GS, Hwang SM, Suh MK, Ha GY, Jang TJ. A case of rosacea-like tinea faciei caused by Trichophyton rubrum. Korean J Med Mycol 2010;15:22-6.

47. Kim I, Bang YJ, Jun JB, Park KD, Chung H, Park J. The clinical and mycological study of tinea faciei in Daegu. Korean J Med Mycol 2015;20:63-9.

48. Shin DH and Kim KH. Clinical and mycologic studies of tinea cruris. Korean J Dermatol 1999;37:219-24.

49. Lim JW, Suh MK, Ha GY. The frequency of tinea pedis in patients with tinea cruris. Korean J Med Mycol 2007;12:1-8.

50. Daniel CR 3rd, Gupta AK, Daniel MP, Daniel CM. Two feet-one hand syndrome: a retrospective multicenter survey. Int J Dermatol 1997;36:658-60.

51. Mochizuki T, Takeda K, Nakagawa M, Kawasaki M, Tanabe H, Ishizaki H. The first isolation in Japan of Trichophyton mentagrophytes var. erinacei causing tinea manuum. Int J Dermatol 2005;44:765-8.

52. Rhee DY, Kim MS, Chang SE, Lee MW, Choi JH, Moon KC, et al. A case of tinea manuum caused by Trichophyton mentagrophytes var. erinacei: the first isolation in Korea. Mycoses 2009;52:287-90.

53. Lim JH, Kim HS, Kim HO, Cho BK, Kim SI, Choi JS, et al. Tinea manus caused by Trichophyton mentagrophytes var. erinacei transferred from a hedgehog. Korean J Dermatol 2009;47:504-7.

54. Lee S and Ahn HJ. Pustular tinea manuum in a child caused by Trichophyton erinacei from a pet hedgehog. Korean J Dermatol 2023;61:204-6.

55. Ko D, Kim I, Chae I, Park KD, Chung H, Bang YJ, et al. The clinical and mycological study of tinea manus and concomitant dermatophytosis. Korean J Med Mycol 2013;18:102-10.

56. Lee JH, Kang JW, Nam MW, Lee JS. Investigating the diagnostic utility of potassium hydroxide (KOH) smear test and the influence of clinical and practical factors in onychomycosis. Korean J Dermatol 2024;62:228-33.

57. Baek G, Koo T, Lee D, Kang HJ, Kim MS, Kim Y, et al. Histopathological examination of the nail plate and comparison between periodic acid-schiff and gomori’s methenamine silver stains for the diagnosis of onychomycosis. Korean J Dermatol 2021;59:618-23.

58. Jung MY, Shim JH, Lee JH, Lee JH, Yang JM, Lee DY, et al. Comparison of diagnostic methods for onychomycosis, and proposal of a diagnostic algorithm. Clin Exp Dermatol 2015;40:479-84.