Abstract
Background
Tinea capitis (TC) is a dermatophytosis of the scalp and hair, which occurs less common in children younger than two years of age, and the data of TC in this age group are still unknown.
Objectives
We aimed to reveal the epidemiological, clinical and mycological characteristics of TC in children under two years old.
Methods
We retrospectively analyzed all reported cases of TC in children in their first two years of life from 1991 to 2022, by searching PubMed, Embase, Web of Science, CNKI, Wanfang and Weipu databases.
Results
A total of 47 articles involving 126 cases of pediatric TC were enrolled in this study. The sex ratio (M/F) was 1.28:1. The age of the children ranged from ten days old to two years old with a median age of three months. The main clinical manifestations were alopecic patches (40 cases, 31.7%) and scaling (39 cases, 31.0%) on the scalp, and 29 infants (23.0%) appeared kerion. The most common sources of contagion were animals (35 cases, 27.78%) and humans (31 cases, 24.60%). The leading pathogens were Microsporidium canis (64 cases, 50.79%), followed by Trichophyton violaceum (13 cases, 10.32%), T. mentagrophytes complex (12 cases, 9.52%) and T. tonsurans (10 cases, 7.94%). Ninety-five children (75.40%) were treated with systemic antifungal drugs and 22 patients (17.46%) were only treated with topical therapy. Except for 10 patients with unknown final prognosis, all the other cases were cured after treatment. There was one child (0.79%) relapsed after treatment with griseofulvin and one case (0.79%) presented with gastrointestinal symptoms from griseofulvin.
Conclusion
The principal clinical symptoms of TC in children less than two years old were alopecic patches and scaling. The top four pathogens were M. canis, T. violaceum, T. mentagrophytes complex and T. tonsurans. Oral treatment for pediatric TC had achieved good therapeutic effects, and topical therapy can be an alternative choice.
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Introduction
Tinea capitis (TC) is a dermatophyte infection of the scalp and hair that appears most common in children, especially preschool children between 3 and 7 years old [1]. It rarely occurs in children in their first two years of life, and there are only a few literatures reporting this age group population and most of them are case reports [2, 3]. Therefore, the epidemiological, clinical and mycological characteristics of pediatric TC in children less than two years old are still unknown. Clinically, pediatric TC can vary considerably, including scaling, annular erythema, alopecia, broken hairs or even kerion, which often leads to misdiagnosis, such as seborrheic dermatitis, neonatal lupus erythematosus, impetigo or atopic dermatitis [4, 5]. If the diagnosis and treatment are not timely, it will cause serious consequences, and even permanent hair loss. Systemic antifungal therapy is the standard for TC, however, for a majority of countries there has been no Food and Drug Administration (FDA) approved oral drugs for the children under two years old [6]. In addition, there is still a lack of research or guidelines for what kind of therapy should be recommended in this age group, which limits clinical treatment. In this study, we systematically reviewed all literatures and summarized the epidemiology, clinical features, pathogens and treatment strategies of TC in children younger than two years old, in order to provide effective information and recommendations on the treatment for clinicians.
Methods
We reviewed all cases in children less than two years of age with an established diagnosis of TC from 1991 to 2022 (32 years), using the key search terms (“tinea capitis” OR “kerion” OR “favus”) AND (“children” OR “infant” OR “newborn” OR “neonate” OR “pediatric” OR “younger than two years old”). A search for all studies (case reports, case series, retrospective or prospective trials) were performed in the following foreign and domestic databases: PubMed, Embase, Web of Science, CNKI (http://www.cnki.net/), WanFang (http://www.wanfangdata.com.cn/) and WeiPu (http://www.cqvip.com/). Titles and abstracts from initial search were reviewed. Inclusion criteria were as follows: (i) studies published in either English or Chinese; (ii) articles published from 1991 to 2022; (iii) included patients’ age under 2 years old; (vi) established diagnosis of TC. The remaining studies were reviewed in detail and studies with obvious wrong or unclear records of data were excluded. Data on demographics, source of contagion, clinical presentation, pathogen, treatment, drug safety and prognosis were extracted from qualified studies and were analyzed using descriptive statistics.
Results
A total of 651 articles were retrieved by using the key search terms, and 47 articles were qualified according to the inclusion and exclusion criteria. One hundred and twenty-six cases of TC in children less than 2 years old from 14 countries were included and analyzed (Tables 1 and 2).
Epidemiological Features
Males (68 cases, 56.20%) of pediatric TC were slightly higher than females (53 cases, 43.80%) with a sex ratio (M/F) of 1.28:1. The other nine patients’ gender information were not available in the literatures. The patients’ age ranged from 10 days old to 2 years old with a median age of 3 months, among them, children younger than 6 months old accounted for the highest proportion of 46.03% (Fig. 1). The duration of the disease prior to diagnosis ranged from 3 to 270 days (median = 30 days). A total of 30 cases (23.8%) had a clear history of misdiagnosis as seborrheic dermatitis, eczema, impetigo or neonatal lupus, treated with topical steroid cream (13 cases) and systemic or topical antibiotics (12 cases), which aggravated the lesions and even evolved into kerion. Animals (35 cases, 27.78%) were the most common source of contagion, followed by humans (31 cases), accounting for 24.60% (Fig. 2).
Clinical Manifestations and Pathogens
The clinical presentation of pediatric TC was variable, and the main clinical manifestations were alopecic patches (40 cases, 31.7%) and scaling (39 cases, 31.0%) on the scalp. Twenty-nine children (23.0%) appeared follicular pustules with exudative or overlying crust on alopecic patches, suggesting a kerion. Four cases (3.17%) and one case (0.79%) were diagnosed as black-dot tinea and favus due to T. mentagrophytes var. quinckeanum, respectively. The other thirteen patients’ clinical manifestations were not described in detail. There were 12 species of dermatophytes isolated from patients. The most predominate pathogens were M. canis (64 cases, 50.79%), followed by T. violaceum (13 cases, 10.32%), T. mentagrophytes complex (12 cases, 9.52%) and T. tonsurans (10 cases, 7.94%). Other strains were only reported in several cases, besides, a case of TC in a newborn was found caused by two organisms, T. rubrum and T. mentagrophytes complex (Fig. 3).
Treatment and Prognosis
Ninety-five children (75.4%) were treated with systemic antifungal drugs, including 64 patients with griseofulvin, 13 patients with itraconazole, 8 patients with terbinafine, 7 patients with fluconazole, and 3 patients with two oral antifungal drugs for the former one ineffective. Besides, 22 patients (17.46%) were only treated with topical therapy, and 9 patients’ treatment strategy were unknown (Fig. 4). Except for 10 patients with unknown final prognosis, all the other cases were cured after treatment and one patient relapsed after treatment with griseofulvin 20 mg/kg/d for two months, who was cured after giving griseofulvin for another one month. There were almost no drug-related side effects except one child (0.79%) presented with gastrointestinal symptoms from griseofulvin, who got better after stopping the drug.
Discussion
We systemically reviewed all articles published in English and Chinese referring to TC in children less than two years old. This study revealed the epidemiological features and treatment recommendations of pediatric TC, providing valuable information for the diagnosis and treatment of TC in children under two years old.
Overall, the data on TC in this age group are limited because of the unusual and low reported prevalence. Children aged 3 ~ 7 years old remain the most commonly affected [1]. We found that the epidemiology, pathogen spectrum and clinical presentation of TC in children younger than two years old were similar to those older than two years old [50], and different from TC in adults [51]. In infants and children, boys were slightly more susceptible to TC than girls (1.28:1), which may be attributed to boys having short hair, more contact with animals and more outdoor physical activities [52]. We confirmed that the top four pathogens were M. canis, T. violaceum, T. mentagrophytes complex and T. tonsurans. The most common zoophilic species were M. canis, followed by T. mentagrophytes complex, which can cause dermatophytosis in animals, and indirectly infect humans through close contact [53]. The most commonly isolated anthropophilic dermatophytes were T. violaceum and T. tonsurans, and mothers were the main source of contagion, who acted as symptomatic or asymptomatic carriers of the anthropophilic pathogens. TC may be seen in various clinical presentation, including hair loss, scaling, black dots, follicular pustules and kerions, depending on the species of dermatophytes, the phase of infection and the immune status of the host [54]. The symptoms of TC in children younger than two years old were similar to older children, and alopecic patches and scaling were noted as the most common types. Therefore, the diagnosis of TC should be considered when an infant presents with scaling, alopecic patches or broken hair on the scalp [23].
Historical data revealed that the fungal distribution pattern of TC in children varied in different countries and times [55]. In China, with the development of economy, the improvement of sanitation and social changes, zoophilic fungi (M. canis) are gradually replacing anthropophilic fungi (T. schoenleinii and T. violaceum) as the most prevalent agent of TC [56]. In Central Europe and the Mediterranean countries, pets are becoming the most likely sources of contagion and TC is predominantly due to M.canis [57]. Whereas in the USA, France and the UK, due to the increase in the immigration of people with African origin, most cases of TC are caused by T. tonsurans [58, 59]. In some Africa areas, TC has always been a serious problem for the poor hygiene and socioeconomic conditions, and dermatophytes with partial geographical restriction, like T. violaceum and T. soudanense, were the leading pathogens [60, 61]. In our study, for the limited cases of TC in younger children, we didn’t find the significant differences in fungal profiles across countries and regions.
Clinically, systemic antifungal drugs have always been recommended for the successful treatment of TC. Since 1959, griseofulvin remains the gold standard of systemic therapy for TC, but high doses and long treatment periods are warranted [62]. The newer antifungal agents terbinafine, itraconazole and fluconazole are now being used more frequently for TC especially in children older than 2 years old, with good efficacy and safety but a reduced treatment duration [6, 63]. However, for the majority of countries in the world, there are still no FDA approved oral agents or treatment guidelines of TC for the children less than two years of age [64]. Till now, there is controversy on whether systemic or topical treatment should be used for TC in this age group. There are mainly two sides of cautious. For one hand, systemic therapy is an off-label treatment, and drug risks limit the use of oral drugs. For the other hand, although topical therapy is felt to be safer for infants, TC usually causes infection at the root of the hair follicle deep within the dermis, and topical treatment alone cannot completely clear the fungus, resulting in higher recurrence rates. In our literature review, we noted that both oral and topical drugs have achieved good therapeutic effects, and almost no reported side effects and recurrence were noted during the whole treatment period and follow up. Besides, Chen et al. [65] found that oral itraconazole was safe and effective in infants and the profiles of adverse events were similar to those in adults and older children through a retrospective analysis of a large number of articles. These results remind us oral antifungal drugs, including griseofulvin, itraconazole, terbinafine and fluconazole, have few adverse effects and topical treatment can be an alternative choice, furthermore, the issues of drug safety and recurrence are not as many as we worried about.
Here, we give the following treatment recommendation for pediatric TC in children under two years old according to these acquired data: (i) children with consent of the guardian or severe clinical symptoms, treatment with systemic antifungal drugs should be recommended, and adverse reactions can be monitored; (ii) infants, especially neonates, with mild symptoms, underlying diseases or no agreement of their guardian, topical therapy should be considered; (iii) the combination of topical and systemic treatment for severe patients might increase the cure rate and shorten the duration of systemic antifungal drugs; (vi) topical cream and antimycotic shampoo can be applied to reduce the transmission of infection and to decrease shedding of infected fungal elements [4].
In this study, we systematically summarized the epidemiological, clinical and pathogenic characteristics of TC in children less than two years old, and based on these data analysis, we gave the treatment recommendation. Oral treatment for pediatric TC were safe, and topical therapy can be an alternative choice, achieving good therapeutic effects. In sum, it is of great significance to improve the treatment for pediatric TC in younger children.
References
Leung AKC, Hon KL, Leong KF, Barankin B, Lam JM. Tinea capitis: an updated review. Recent Pat Inflamm Allergy Drug Discov. 2020;14(1):58–68. https://doi.org/10.2174/1872213x14666200106145624.
Mandras N, Roana J, Cervetti O, Panzone M, Tullio V. A case report of tinea capitis in infant in first year of life. BMC Pediatr. 2019;19(1):65. https://doi.org/10.1186/s12887-019-1433-7.
Toyosawa Y, Kimura U, Kurihara M, Noguchi H, Matsumoto T, Hiruma M, et al. Kerion Celsi caused by nannizzia gypsea in a two-year-old child who had been hospitalized since birth. Med Mycol J. 2022;63(1):21–3. https://doi.org/10.3314/mmj.21-00021.
Michaels BD, Del Rosso JQ. Tinea capitis in infants: recognition, evaluation, and management suggestions. J Clin Aesthet Dermatol. 2012;5(2):49–59.
Zampella JG, Kwatra SG, Blanck J, Cohen B. Tinea in tots: cases and literature review of oral antifungal treatment of tinea capitis in children under 2 years of age. J Pediatr. 2017;183:12-8.e3. https://doi.org/10.1016/j.jpeds.2016.12.042.
Chen X, Jiang X, Yang M, Bennett C, González U, Lin X, et al. Systemic antifungal therapy for tinea capitis in children: an abridged cochrane review. J Am Acad Dermatol. 2017;76(2):368–74. https://doi.org/10.1002/14651858.CD004685.pub3.
Gondim-Gonçalves HM, Mapurunga AC, Melo-Monteiro C, Lima AA. Tinea capitis caused by Microsporum canis in a newborn. Int J Dermatol. 1992;31(5):367. https://doi.org/10.1111/j.1365-4362.1992.tb03964.x.
Snider R, Landers S, Levy ML. The ringworm riddle: an outbreak of Microsporum canis in the nursery. Pediatr Infect Dis J. 1993;12(2):145–8.
Virgili A, Corazza M, Zampino MR. Atypical features of tinea in newborns. Pediatr Dermatol. 1993;10(1):92. https://doi.org/10.1111/j.1525-1470.1993.tb00027.x.
Cabon N, Moulinier C, Taieb A, Maleville J. Tinea capitis and faciei caused by Microsporon langeronii in two neonates. Pediatr Dermatol. 1994;11(3):281. https://doi.org/10.1111/j.1525-1470.1994.tb00607.x.
Ghorpade A, Ramanan C. Tinea capitis and corporis due to Trichophyton violaceum in a six-day-old infant. Int J Dermatol. 1994;33(3):219–20.
García-Sánchez MS, Pereiro M Jr, Pereiro MM, Toribio J. Favus due to Trichophyton mentagrophytes var. quinckeanum. Dermatol (Basel, Switz). 1997;194(2):177–9. https://doi.org/10.1159/000246092.
Ungar SL, Laude TA. Tinea capitis in a newborn caused by two organisms. Pediatr Dermatol. 1997;14(3):229–30. https://doi.org/10.1111/j.1525-1470.1997.tb00245.x.
Weston WL, Morelli JG. Neonatal tinea capitis. Pediatr Infect Dis J. 1998;17(3):257–8. https://doi.org/10.1097/00006454-199803000-00021.
Wilmer A, Wollina U. Oral terbinafine in the treatment of griseofulvin-resistant Tinea capitis et faciei et corporis in a 10-month-old girl. Acta Derm Venereol. 1998;78(4):314. https://doi.org/10.1080/000155598442052.
Romano C. Case reports. Four paediatric cases of tinea capitis due to unusual agents. Mycoses. 1999;42(5–6):421–5. https://doi.org/10.1046/j.1439-0507.1999.00494.x.
Ginarte M, Pereiro M Jr, Fernández-Redondo V, Toribio J. Case reports. Pityriasis amiantacea as manifestation of tinea capitis due to Microsporum canis. Mycoses. 2000;43(1–2):93–6. https://doi.org/10.1046/j.1439-0507.2000.00543.x.
Koumantaki E, Georgala S, Rallis E, Papadavid E. Microsporum canis tinea capitis in an 8-month-old infant successfully treated with 2 weekly pulses of oral itraconazole. Pediatr Dermatol. 2001;18(1):60–2. https://doi.org/10.1046/j.1525-1470.2001.018001060.x.
Romano C, Gianni C, Papini M. Tinea capitis in infants less than 1 year of age. Pediatr Dermatol. 2001;18(6):465–8. https://doi.org/10.1046/j.1525-1470.2001.1861997.x.
Chang SE, Kang SK, Choi JH, Sung KJ, Moon KC, Koh JK. Tinea capitis due to Trichophyton rubrum in a neonate. Pediatr Dermatol. 2002;19(4):356–8. https://doi.org/10.1046/j.1525-1470.2002.00100.x.
Gilaberte Y, Rezusta A, Coscojuela C. Tinea capitis in a newborn infected by Microsporum audouinii in Spain. J Eur Acad Dermatol Venereol JEADV. 2003;17(2):239–40. https://doi.org/10.1046/j.1468-3083.2003.00577_10.x.
Aste N, Pinna AL, Pau M, Biggio P. Kerion Celsi in a newborn due to Microsporum canis. Mycoses. 2004;47(5–6):236–7. https://doi.org/10.1111/j.1439-0507.2004.00967.x.
Gilaberte Y, Rezusta A, Gil J, Sáenz-Santamaría MC, Coscojuela C, Navarro M, et al. Tinea capitis in infants in their first year of life. Br J Dermatol. 2004;151(4):886–90. https://doi.org/10.1111/j.1365-2133.2004.06112.x.
Valari M, Stefanaki C, Karteri G, Zarkadi E, Katsambas A. Tinea capitis due to Trichophyton rubrum in a 3-month-old infant. Mycoses. 2006;49(5):439–40. https://doi.org/10.1111/j.1439-0507.2006.01267.x.
Binder B, Richtig E, Weger W, Ginter-Hanselmayer G. Tinea capitis in early infancy treated with itraconazole: a pilot study. J Eur Acad Dermatol Venereol JEADV. 2009;23(10):1161–3. https://doi.org/10.1111/j.1468-3083.2009.03271.x.
Larralde M, Gomar B, Boggio P, Abad ME, Pagotto B. Neonatal kerion Celsi: report of three cases. Pediatr Dermatol. 2010;27(4):361–3. https://doi.org/10.1111/j.1525-1470.2010.01169.x.
Atanasovski M, El Tal AK, Hamzavi F, Mehregan DA. Neonatal dermatophytosis: report of a case and review of the literature. Pediatr Dermatol. 2011;28(2):185–8. https://doi.org/10.1111/j.1525-1470.2010.01318.x.
Mapelli ET, Borghi E, Cerri A, Sciota R, Morace G, Menni S. Tinea corporis due to Trichophyton rubrum in a woman and Tinea capitis in her 15-day-old baby: molecular evidence of vertical transmission. Mycopathologia. 2012;173(2–3):135–8. https://doi.org/10.1007/s11046-011-9492-9.
Zaraa I, Hawilo A, Trojjet S, El Euch D, Mokni M, Ben OA. Letter: Tinea capitis in infants in their first 2 years of life: a 12-year study and a review of the literature. Dermatol Online J. 2012;18(7):16.
Ambooken B, Binitha MP, Chandran B. Kerion due to microsporum gypseum in a 1-month-old infant. Int J Trichol. 2013;5(4):214–6. https://doi.org/10.4103/0974-7753.130418.
Berry A, Abramovici G, Chamlin SL. A 21-day-old boy with an annular eruption. Tinea faciei/Tinea capitis. Pediatr Ann. 2014;43(1):e16-8. https://doi.org/10.3928/00904481-20131223-12.
Hudgins E, Wine Lee L, Castelo-Soccio L. A 24-day-old neonate with annular plaques on the scalp. JAMA Pediatr. 2015;169(1):93–4. https://doi.org/10.1001/jamapediatrics.2014.1848.
Fremerey C, Nenoff P. Tinea capitis in a newborn. N Engl J Med. 2018;378(21):2022. https://doi.org/10.1056/NEJMicm1711862.
Kumar P, Pandhi D. Role of trichoscopy in the management of tinea capitis in two infants: a case report. J Cutan Aesthet Surg. 2021;14(4):443–5. https://doi.org/10.4103/jcas.Jcas_160_20.
Chen RE, Sun ZJ, Wan JZ. A case of kerion and tinea corporis in infants caused by Microsporum fuentcs. Chin J Dermatol (In Chin). 2001;34(6):434. https://doi.org/10.3760/j.issn:0412-4030.2001.06.034.
Lu GX, Tao SQ, Shen YN, Chen F, Liu WD. A case report of “black dot tinea” caused by a variant species of Trichophyton tonsurans cured with terbinafine. J Clin Dermatol (In Chin). 2001;30(3):183–4. https://doi.org/10.3969/j.issn.1000-4963.2001.03.027.
Zhu LX, Sun ZZ. Kerion cured with itraconazole in an infant. Chin J Dermatol (In Chin). 2006;36(1):40.
Chen J, Zhou L. A case of tinea capifis varnigra caused by trichophyton violaceum. Chin J Derm Venereol. 2017;21(6):362–3. https://doi.org/10.3969/j.issn.1001-7089.2007.06.020.
Gao ZQ, Li JL, Gu WL. A case of infant tinea capitis. J Clin Dermatol. 2007;36(5):322–3. https://doi.org/10.3969/j.issn.1000-4963.2007.05.028.
Xing FS, Hu ZM, Jiang P, Sun ZZ. A case of Infant Kerion with tinea corporis. Chin J Derm Venereol (In Chin). 2009;23(1):52–3.
Wang J, Xu YC, Ju Y, Ren RX, He YX. Three cases of neonatal tinea capitis caused by Microsporum canis. Med J Natl Defending Forces Northeast China (In Chin). 2011;32(1):6.
Jing DY. Kerion due to Trichophyton mentagrophytes in an infant. China J Lepr Skin Dis (In Chin). 2014;30(2):119–20.
Tang JQ, Zhuang KW, Ran X, Ran YP. A case of infant kerion with dermatophytid reaction due to Trichophyton tonsurans. Chin J Mycol (In Chin). 2016;11(3):185–6.
Wang YN, Chen XJ, Xia XJ, Hang CY. A case of infant kerion. Chin J Dermatol (In Chin). 2017;50(11):794. https://doi.org/10.3760/cma.j.issn.0412-4030.2017.11.004.
Chen J, Wang CC, Zhang Y, Nie ZH, Li GZ. A case of tinea capitis in infant caused by Trichophyton violaceum. Chin J Dermato Venerol Integ Trad W Med (In Chin). 2007;21(6):69–70. https://doi.org/10.3969/j.issn.1672-0709.2017.01.023.
Guo YY, Fu M, Ma CL. Tinea capitis in a newborn caused by Microsporum canis: a case report. Chin J Mycol (In Chin). 2018;13(4):239–40.
Huang MN, Zhu HL, Xiong CP. A case of infant black-dot ringworm. J Diagn Ther Dermato-Venereol. 2020;27(6):438–40. https://doi.org/10.3969/j.issn.1674-8468.2020.06.015.
Xiao YY, Zhou YB, Chao JJ, Ma L. Successful treatment of tinea capitis caused by Microsporum canis in a 23-day-old newborn with itraconazole pulse therapy and a review of the literature. Dermatol Ther. 2021;34(5):e15078. https://doi.org/10.1111/dth.15078.
Zhou YB, Chao JJ, Xiao YY, Ma L. High-dose oral terbinafine in the treatment of pediatric tinea capitis under 2 years old. Dermatol Ther. 2022;35(4):e15320. https://doi.org/10.1111/dth.15320.
Chen XQ, Zheng DY, Xiao YY, Dong BL, Cao CW, Ma L, et al. Aetiology of tinea capitis in China: a multicentre prospective study. Br J Dermatol. 2021. https://doi.org/10.1111/bjd.20875.
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(8):876–88. https://doi.org/10.1111/myc.13102.
Getso MI, Hashemi SJ, Ghazvini RD, Yusuf SM, Khodavaisy S, Gerami-Shoar M, et al. Determination of dermatophytes isolated from tinea capitis using conventional and ITS-based sequencing methods in Kano, Nigeria. J de Mycologie Medicale. 2021;31(3):101157. https://doi.org/10.1016/j.mycmed.2021.101157.
Moriello KA, Coyner K, Paterson S, Mignon B. Diagnosis and treatment of dermatophytosis in dogs and cats: clinical consensus guidelines of the world association for veterinary dermatology. Vet Dermatol. 2017;28(3):266-e68. https://doi.org/10.1111/vde.12440.
Celestrino GA, Verrinder Veasey J, Benard G, Sousa MGT. Host immune responses in dermatophytes infection. Mycoses. 2021;64(5):477–83. https://doi.org/10.1111/myc.13246.
Elewski BE. Tinea capitis: a current perspective. J Am Acad Dermatol. 2000;42(1 Pt 1):1–20. https://doi.org/10.1016/s0190-9622(00)90001-x.
Zhan P, Li D, Wang C, Sun J, Geng C, Xiong Z, et al. Epidemiological changes in tinea capitis over the sixty years of economic growth in China. Med Mycol. 2015;53(7):691–8. https://doi.org/10.1093/mmy/myv057.
Ginter-Hanselmayer G, Weger W, Ilkit M, Smolle J. Epidemiology of tinea capitis in Europe: current state and changing patterns. Mycoses. 2007;50(Suppl 2):6–13. https://doi.org/10.1111/j.1439-0507.2007.01424.x.
Suh DC, Friedlander SF, Raut M, Chang J, Vo L, Shin HC, et al. Tinea capitis in the United States: diagnosis, treatment, and costs. J Am Acad Dermatol. 2006;55(6):1111–2. https://doi.org/10.1016/j.jaad.2006.08.056.
Ferguson L, Fuller LC. Spectrum and burden of dermatophytes in children. J Infect. 2017;74(Suppl 1):S54-s60. https://doi.org/10.1016/s0163-4453(17)30192-5.
Bongomin F, Olum R, Nsenga L, Namusobya M, Russell L, de Sousa E, et al. Estimation of the burden of tinea capitis among children in Africa. Mycoses. 2021;64(4):349–63. https://doi.org/10.1111/myc.13221.
Coulibaly O, L’Ollivier C, Piarroux R, Ranque S. Epidemiology of human dermatophytoses in Africa. Med Mycol. 2018;56(2):145–61. https://doi.org/10.1093/mmy/myx048.
Bennett ML, Fleischer AB, Loveless JW, Feldman SR. Oral griseofulvin remains the treatment of choice for tinea capitis in children. Pediatr Dermatol. 2000;17(4):304–9. https://doi.org/10.1046/j.1525-1470.2000.01784.x.
Chen X, Jiang X, Yang M, González U, Lin X, Hua X, et al. Systemic antifungal therapy for tinea capitis in children. Cochrane Database Syst Rev. 2016;2016(5):cd004685. https://doi.org/10.1016/j.jaad.2016.08.061.
Chan YC, Friedlander SF. Therapeutic options in the treatment of tinea capitis. Expert Opin Pharmacother. 2004;5(2):219–27. https://doi.org/10.1517/14656566.5.2.219.
Chen S, Sun KY, Feng XW, Ran X, Lama J, Ran YP. Efficacy and safety of itraconazole use in infants. World J Pediatr WJP. 2016;12(4):399–407. https://doi.org/10.1007/s12519-016-0034-x.
Funding
This work was funded by China National Key R&D Program during the 14th Five-year Plan Period (Grant No.2022YFC2504804); National Natural Science Foundation of China (Grant No. 81972949); CAMS Innovation Fund for Medical Sciences (CIFMS) (Grant No. 2021-I2M-1-039); The National Science and Technology Infrastructure of China (Grant No. NPRC-32) and The Basic Scientific Research Fund Projects of Chinese Academy of Medical Sciences (Grant No. 2021-PT310-006).
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GZL contributed to the study conception and design. Data collection and analysis were performed by GS, MJZ and XK. The first draft of the manuscript was written by GS and the revision of the article was done by GZL and WDL. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
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Song, G., Zhang, M., Kong, X. et al. Tinea Capitis in Children Younger than Two Years Old: A Retrospective Study and Treatment Recommendations. Mycopathologia 188, 461–478 (2023). https://doi.org/10.1007/s11046-022-00703-z
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DOI: https://doi.org/10.1007/s11046-022-00703-z