|Year : 2020 | Volume
| Issue : 2 | Page : 68-74
Trichoscopy as a diagnostic tool for tinea capitis: A prospective, observational study
Pradeep Kumar1, Deepika Pandhi1, Sambit Nath Bhattacharya1, Shukla Das2
1 Department of Dermatology and STD, University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi, India
2 Department of Microbiology, University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi, India
|Date of Submission||07-Mar-2020|
|Date of Decision||17-Mar-2020|
|Date of Acceptance||07-Apr-2020|
|Date of Web Publication||05-May-2020|
Department of Dermatology and STD, University College of Medical Sciences and Associated GTB Hospital, Delhi - 110 095
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Tinea capitis is the most common pediatric dermatophyte infection. Trichoscopy aids in the rapid diagnosis and allows prompt treatment, preventing horizontal transmission. Objectives: The objective of this study is to document the trichoscopic features of tinea capitis and evaluate its correlation with clinical type, microscopic form, and mycological culture and propose diagnostic trichoscopic criteria.Materials and Methods: Trichoscopy was performed, after taking consent in 98 participants (<18 years) of tinea capitis diagnose by hair root and scalp scraping examination for hyphae positive on potassium hydroxide mount microscopy or culture positive on SDA media. The comparison of observed trichoscopic features, with the clinical type, pattern of invasion, and etiological agent was carried out. Results: The most common clinical variant was black dot, and etiological agent was Trichophyton violaceum. The following trichoscopic features were noted: black dot, comma, short broken, corkscrew, horse-shoe, zigzag hair, and perifollicular scaling. Perifollicular scaling was significantly common in gray-patch variant, whereas comma, black dot, horse-shoe hair, and perifollicular scaling were noted in black-dot variant. Comma, corkscrew, and zig-zag hair were significantly present in endothrix form, whereas perifollicular scaling was evident in ectothrix form. Combining perifollicular scaling with comma hair, short broken, and black dot hair achieved a diagnostic sensitivity of 98.97%. Conclusions: Trichoscopy by evaluating for the combination of perifollicular scaling and 3 dystrophic hair (comma hair, black dot, and short-broken hair) is a good diagnostic tool for tinea capitis. Horse-shoe hair a novel finding, not hitherto reported in the literature requires validation in future studies.
Keywords: Comma hair, cork-screw hair, horse-shoe hair, tinea capitis, trichoscopy, zigzag hair
|How to cite this article:|
Kumar P, Pandhi D, Bhattacharya SN, Das S. Trichoscopy as a diagnostic tool for tinea capitis: A prospective, observational study. Int J Trichol 2020;12:68-74
|How to cite this URL:|
Kumar P, Pandhi D, Bhattacharya SN, Das S. Trichoscopy as a diagnostic tool for tinea capitis: A prospective, observational study. Int J Trichol [serial online] 2020 [cited 2020 Oct 26];12:68-74. Available from: https://www.ijtrichology.com/text.asp?2020/12/2/68/283806
| Introduction|| |
Tinea capitis is the most frequent manifestation of dermatophyte infection in children, especially in the lower socioeconomic strata. The three clinical types of tinea capitis have been described: non-inflammatory variants (gray patch, black dot, seborrheic, and alopecia areata-like), inflammatory variants (kerion, favus, and pustular-like), and mixed pattern (new variant) associated with slow onset and extensive involvement.,
Epidemiology of tinea capitis varies greatly with respect to its geographic location and specific population groups. Among children, the worldwide prevalence of tinea capitis varies from 7.1% to 47.5%, and the incidence in India is 0.5% to 10%., Currently, Trichophyton tonsurans and Microsporum canis are the leading causes of tinea capitis in children in the United States and Europe, respectively. In the Indian population, Trichophyton violaceum was the most common etiological agent during the period of 2006–2010 with isolation rates of 30%–88%.,, Geographical distribution within India varies with T. violaceum (88.6%) being the most common etiological agent in North India, Trichophyton mentagrophytes complex (43%) in hilly areas of India, Trichophyton rubrum (21.8%) in South India, and Trichophyton tonsurans (61.1%) in Kashmir.,,,
Tinea capitis is screened by microscopy (10% potassium hydroxide [KOH] hair mount) and confirmed by growth in Sabouraud dextrose agar (SDA) culture media that takes 3–4 weeks, with resultant delayed treatment and increase in the risk of horizontal transmission. Therefore, trichoscopy can aid in the early diagnosis (without need for expert opinion for the interpretation of trichoscopic features) and prompt treatment to avoid contamination and complications such as cicatricial alopecia (as occurs in inflammatory variant). However, studies regarding the trichoscopic findings of patients with tinea capitis are relatively uncommon.,,,,, Therefore, the present study has been designed to establish the utility of trichoscopy as a diagnostic tool in tinea capitis and to determine the correlation of the etiological agent, pattern of invasion, and clinical types with trichoscopic changes, if any.
| Materials and Methods|| |
We carried out an observational, descriptive study over 18 months, after obtaining approval from the Institutional Ethics Committee. We recruited 98 (<18 years) with suspected tinea capitis (patchy alopecia, scaling, broken hair, pustules, boggy swelling, and cervical lymphadenopathy) that were positive for hyphae (endothrix or ectothrix) on 10% KOH mount microscopy. After a written informed consent, history and detailed clinical examination were carried out including scalp site examination and evaluation for lymphadenopathy, coexistent fungal infection (including nail), and associated diseases (nonfungal). A clinical photograph was taken, and trichoscopic examination of the most affected scalp lesion was performed. This was done by USB dermatoscope: AM7013MZTS Dino-Lite Premier (AnMo Electronics Corporation, Taiwan, China), and the trichoscopic findings were noted at ×70 and ×170 in polarized and nonpolarized mode. These features were evaluated by the single observer. Subsequently, extracted hair root and scalp scraping of the recruited participants were sent for Sabouraud's dextrose agar culture.
The statistical analysis was performed using the IBM SPSS software version 20.0 (IBM Corp., Armonk, Chicago, IL, NY; USA) with a threshold of significance of P (two-tailed) <0.05 (confidence interval = 95%) significant. The comparison of trichoscopic features of tinea capitis with clinical type, pattern of invasion, and mycological culture was done using the Chi-square test.
| Results|| |
The details of the 98 recruited patient's sociodemographic profile are depicted in [Table 1]. Most of the patients (92.85%) were below 12 years, with a peak age range of 4–6 years, and a marginal female preponderance with a male-to-female ratio of 1:1.18.
|Table 1: Sociodemographic profile and various history of 98 study participants|
Click here to view
The duration of tinea capitis varied from 1 to 48 months, with a 50th percentile of 2 ± 3 months (median ± interquartile range [IQR]) and a mean ± standard deviation of 3.79 ± 6.63 months. The most common symptom in tinea capitis was hair loss (94.89%) followed by scaling (86.73%) and pruritus (82.65%) with predominant multifocal scalp involvement. The associated findings included regional lymphadenopathy (65%), tinea faciei (7.14%), tinea manuum (1%), and onychomycosis (1%). The other concurrent diseases were molluscum contagiosum (3.06%), pediculosis capitis, and verruca vulgaris (2.04% each).
The most common clinical type of tinea capitis was black dot (46.93%) followed by gray patch (28.57%), kerion (11.22%), seborrheic variant (7.14%), alopecia areata (3.06%), and the least common was the pustular variant (3.06%). No case of favus was seen in the present study. KOH mount microscopy examination revealed endothrix variant was more common in tinea capitis as compared to ectothrix (74% versus 26%). Endothrix invasion was significantly more in black dot and kerion (P = 0.038) clinical variants. Mycological culture was positive in 51 out of the 98 cases. The most common causative agent in the present study was T. violaceum (86.27%) followed by Trichophyton verrucosum, Trichophyton mentagrophytes complex, Trichophyton tonsurans (each 3.92%), and Trichophyton rubrum (1.96%). No Microsporum species were isolated in our patients.
Hair morphologies observed in tinea capitis on trichoscopy were short-broken hair, comma hair, cork-screw hair, black dot, zigzag hair, i-hair, Morse code hair, horse-shoe hair (novel finding), exclamation hair, flame hair, regrowing hair, and perifollicular scaling.
The frequency of different trichoscopic features of tinea capitis is depicted in [Figure 1]. Black dot (82.65%) was the most common finding followed by comma hair, short-broken hair, perifollicular scaling, cork-screw hair, horse-shoe hair, and zigzag hair. Whereas, other findings such as regrowing hair, i-hair, flame hair, morse code hair, thick scale, erythema, telangiectasia, and hemorrhages (ETH) were observed in one-fifth or fewer cases.
|Figure 1: Frequency of trichoscopic features in 98 children with tinea capitis|
Click here to view
Black dot (P = 0.015) and ETH (P = 0.00) were significantly present in noninflammatory and inflammatory variant of tinea capitis, respectively, on trichoscopy. The clinical types of tinea capitis showed a significant presence of trichoscopic features, like comma hair (P = 0.019), black dot (P = 0.008), horse-shoe hair (P = 0.056, marginal significant), and perifollicular scaling (P = 0.023) in black-dot variant [Figure 2]a and [Figure 2]b and perifollicular scaling (P = 0.03) in gray patch tinea capitis [Figure 3]a and [Figure 3]b. Similarly, black dot (P = 0.021) and ETH (P = 0.001) were significantly present in kerion variety. Endothrix variant showed comma hair, cork-screw hair (P = 0.007 each), zigzag hair (P = 0.011), and horse-shoe hair (P = 0.062, marginal significant) as significant trichoscopic findings. Similarly, a significant presence of perifollicular scaling (P = 0.028) in ectothrix form was noted. Correlating with the etiological agent, comma hair (P = 0.005) was significantly found in tinea capitis caused by T. violaceum [Table 2].
|Figure 2: (a) Clinical image showing black-dot tinea capitis. (b) Trichoscopy (×70 magnification, polarized mode) shows comma hair (red arrow), cork-screw hair (blue arrow) and horse-shoe hair (green arrow) in patient in (a)|
Click here to view
|Figure 3: (a) Clinical image showing gray patch tinea capitis. (b) Trichoscopy (×70 magnification, polarized mode) shows perifollicular scaling (yellow arrow) in the patient in (a)|
Click here to view
|Table 2: Comparison of frequency of trichoscopic features with clinical types, microscopic form, and etiological agents|
Click here to view
The sensitivity (95% confidence interval of mean) of individual trichoscopic features for diagnosing tinea capitis was short-broken hair 53.1% (43.1–63.0), comma hair 57.1% (47.2–66.9), cork-screw hair 32.7% (23.3–42.0), black dot 82.7% (75.1–90.2), and perifollicular scaling 46.9 (36.9–56.8). By combining perifollicular scaling, comma hair, short-broken hair, and black dot, a sensitivity of 98.97% was achieved.
| Discussion|| |
Tinea capitis is a common fungal infection among children (median age ± IQR: 2 ± 3 years) mostly belonging to lower socioeconomic scale, with a slight female predominance. In the present study, 50% cases presented within 3 months of the onset of disease, with an early presentation being observed in the inflammatory variants. Coexisting fungal infection was seen in 13.26% cases that could be attributable to autoinoculation of fungus from the untreated tinea capitis lesions. Culture on SDA media-yielded growth in 52% cases, and only Trichophyton isolates were found. Further, with an 86.7% isolation rate in our study, T. violaceum continues to be the predominant species in north India.
In 2008, Slowinska et al. described for the first time the dermoscopic image finding of comma hair in two children with tinea capitis, due to M. canis. Subsequent studies revealed perifollicular scaling (95%), short-broken hair (74%–100%), comma hair (26%–66%), cork-screw hair (13%–80%), zigzag hair (25%–50%), black dot (13%–65%), i-hair, and Morse code hair (16%–26.5%) as trichoscopic features suggestive of tinea capitis.,,,,,,,,,
There is a paucity of data evaluating trichoscopic features in patients with tinea capitis and the diagnosis of tinea capitis based on trichoscopic diagnostic criteria has not been well established due to low power of the previous studies.,,,,,,,, The various trichoscopic features of tinea capitis in our cohort are depicted in [Table 3] and compared with other studies. Similar to our findings, comparable percentage of black dot, comma hair, cork-screw hair and zigzag hair were reported by El-Taweel et al. and Aqil et al., This could be attributed to a similar profile of etiological agents (most importantly T. violaceum) isolated in these two studies., The most common etiological agent in our study T. violaceum (86.27%) causes hair-shaft deformation without color impairment by endothrix invasion, resulting in comma and corkscrew hair. However, bent hair, forked hair, and V-shaped hair reported by Aqil et al. were not present in our study. Zigzag hair [Figure 4], horse-shoe hair, and regrowing hair were seen in 10%–17% patients, and Morse code hair [Figure 5], flame hair, and i-hair were seen in 2%–7% patients in the present study. Transverse perforation of hair shaft by ectothrix invasion followed by few and several fracture results in Morse code hair and zigzag hair, respectively, and complete transverse fracture produce broken and black-dot hair. Morse code hair and zigzag hair in Caucasians and comma hair in Africans were significantly noted by Dhaille et al. We were unable to correlate trichoscopic hair findings with racial hair types due to similar ethnic profile of our patients. Further, trichoscopic features were independent of gender in our study group, in contrast to the study by Aqil et al., wherein cork-screw hair was significantly present in female children.
|Table 3: Comparative trichoscopic features between our study and other studies|
Click here to view
|Figure 4: Zigzag hair (red arrow) in tinea capitis: (×70, polarized mode)|
Click here to view
|Figure 5: Morse code hair (violet arrow) as trichoscopic finding in tinea capitis (70x magnification, polarised mode)|
Click here to view
Trichoscopy of noninflammatory variant (particularly black-dot tinea capitis) and inflammatory variant (particularly kerion) characteristically showed black dot (in both variants) and ETH, respectively. The ectothrix invasion presenting as gray patch tinea capitis is characterized by perifollicular scaling on trichoscopy. Endothrix invasion causing black-dot tinea capitis is characterized by comma hair (particularly T. violaceum affected cases) and horse-shoe hair. Apart from this, cork-screw hair and zigzag hair were also produced by endothrix invasion. This is in agreement with our study and the findings of Dhaille et al., where corkscrew and comma hair were present in endothrix cases. Zigzag hair has also been described in ectothrix variant by Bourezane and Bourezane.
Horse-shoe hair was a novel finding in the present study, observed in 16% children with tinea capitis (predominantly in the black-dot variety). It is defined as U-shaped hair (resembling horse-shoe) with arms of equal length and could be considered as exacerbation of the comma hair (and hence similar pathogenesis). On SDA culture media, these cases showed T. violaceum (56.25%) as the predominant isolate and a single isolate of Trichophyton mentagrophytes complex was also recovered. This hair pattern was observed in both noninflammatory and inflammatory variants of tinea capitis in the present study.
Tinea capitis cannot be diagnosed by a single trichoscopic feature but requires combination of features such as perifollicular scaling, along with any type of dystrophic hair or broken hairs that have been found to be specific for tinea capitis.,, Brasileiro et al. concluded that a combination of six trichoscopic features (short broken, black dot, comma, corkscrew, zigzag hair, and perifollicular scaling) were essential to make the diagnosis of tinea capitis. In contrast, a recent study by Dhaille et al. suggested that a single trichoscopic feature is predictive of tinea capitis. They reported the sensitivity of a single trichoscopic feature for the prediction of tinea capitis varied from 22.6% to 83% in their study, as compared to our study wherein individual predictive sensitivity varied from 32.7% to 82.7%. It is pertinent to note that our study analyzed 98 confirmed tinea capitis as compared to the study by Dhaille et al., wherein 58 out of the 100 recruited participantts were considered as case of tinea capitis and alternate diagnosis of alopecia areata, trichotillomania, and lichen planopilaris were considered for the other patients. The researchers had included these 58 cases on the basis of presence of at least 2 hair showing tinea capitis specific trichoscopic features and had also excluded kerion case. We found that at least 4 among the above 6 features were consistently present in 97 out of 98 patients in the present study; therefore, we recommend that 4 features (short-broken hair, black dot, comma hair, and perifollicular scaling) are sufficient for diagnosing tinea capitis with a 98.97% sensitivity. Further, we infer that a single trichoscopic feature may lead to a low sensitivity in the diagnosis of tinea capitis.
Limitation of our study was the isolation of only Trichophyton species as etiological agents and absence of any Microsporum species. Therefore, we cannot comment on trichoscopic findings and correlation pertaining to the latter species. Furthermore, Trichophyton species (other than T. violaceum) also had low isolation rates (2%–4%), and their correlation with altered hair morphology on trichoscopy cannot be commented upon. We recommend that in order to establish the correlation between trichoscopic features with etiological agents of tinea capitis, inclusion criteria should include fungal culture-positive cases wherein a minimum number of cases caused by each common causative agent is included.
| Conclusions|| |
Trichoscopy had a sensitivity of 98.97% in diagnosing tinea capitis by considering the combination of perifollicular scaling and 3 dystrophic hair (short-broken hair, comma hair, and black dot). Therefore, we validate that trichoscopy may be rapid diagnostic tool for tinea capitis obviating the need for traditional fungal culture method that takes several weeks. Horse-shoe hair is a novel finding in the present study and needs to be validated in future trichoscopy studies of tinea capitis.
Limitations of the study
The study is limited by the inability to measure and document hair shaft diameter and variability owing to the lack of sophisticated dermoscope-like FotoFinder.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Grover C, Arora P, Manchanda V. Tinea capitis in the pediatric population: A study from North India. Indian J Dermatol Venereol Leprol 2010;76:527-32.
] [Full text]
Bunyaratavej S, Leeyaphan C, Rujitharanawong C, Muanprasat C, Matthapan L. Clinical and laboratory characteristics of a TC outbreak among novice buddhist monks. Pediatr Dermatol 2017;34:371-373.
Leiva-Salinas M, Marin-Cabanas I, Betlloch I, Tesfasmariam A, Reyes F, Belinchon I, et al
. Tinea capitis in schoolchildren in a rural area in Southern Ethiopia. Int J Dermatol 2015;54:800-5.
Pai VV, Hanumanthayya K, Tophakhane RS, Nandihal NW, Kikkeri NS. Clinical study of tinea capitis in Northern Karnataka: A three-year experience at a single institute. Indian Dermatol Online J 2013;4:22-6.
] [Full text]
Hay RJ. Tinea capitis: Current status. Mycopathologia 2017;182:87-93.
Bhat YJ, Zeerak S, Kanth F, Yaseen A, Hassan I, Hakak R. Clinicoepidemiological and mycological study of tinea capitis in the pediatric population of Kashmir Valley: A study from a tertiary care centre. Indian Dermatol Online J 2017;8:100-3.
] [Full text]
Moriarty B, Hay R, Morris-Jones R. The diagnosis and management of tinea. BMJ 2012;345:e4380.
Dhaille F, Dillies AS, Dessirier F, Reygagne P, Diouf M, Baltazard T, et al
. A single typical trichoscopic feature is predictive of tinea capitis: A prospective multicentre study. Br J Dermatol 2019;181:1046-51.
El-Taweel AE, El-Esawy F, Abdel-Salam O. Different trichoscopic features of tinea capitis and alopecia areata in pediatric patients. Dermatol Res Pract 2014;2014:848763.
Brasileiro A, Campos S, Cabete J, Galhardas C, Lencastre A, Serrão V. Trichoscopy as an additional tool for the differential diagnosis of tinea capitis: A prospective clinical study. Br J Dermatol 2016;175:208-9.
Bourezane Y, Bourezane Y. Analysis of trichoscopic signs observed in 24 patients presenting tinea capitis: Hypotheses based on physiopathology and proposed new classification. Ann Dermatol Venereol 2017;144:490-6.
Ekiz O, Sen BB, Rifaioǧlu EN, Balta I. Trichoscopy in paediatric patients with tinea capitis: A useful method to differentiate from alopecia areata. J Eur Acad Dermatol Venereol 2014;28:1255-8.
Aqil N, BayBay H, Moustaide K, Douhi Z, Elloudi S, Mernissi FZ. A prospective study of tinea capitis in children: Making the diagnosis easier with a dermoscope. J Med Case Rep 2018;12:383.
Slowinska M, Rudnicka L, Schwartz RA, Kowalska-Oledzka E, Rakowska A, Sicinska J, et al
. Comma hairs: A dermatoscopic marker for tinea capitis: A rapid diagnostic method. J Am Acad Dermatol 2008;59:S77-9.
Hughes R, Chiaverini C, Bahadoran P, Lacour JP. Corkscrew hair: A new dermoscopic sign for diagnosis of tinea capitis in black children. Arch Dermatol 2011;147:355-6.
Mapelli ET, Gualandri L, Cerri A, Menni S. Comma hairs in tinea capitis: A useful dermatoscopic sign for diagnosis of tinea capitis. Pediatr Dermatol 2012;29:223-4.
Sandoval AB, Ortiz JA, Rodríguez JM, Vargas AG, Quintero DG. Dermoscopic pattern in tinea capitis. Rev Iberoam Micol 2010;27:151-2.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
[Table 1], [Table 2], [Table 3]