Tinea capitis is perhaps the most common mycotic infection in children. In
North America the epidemiology of tinea capitis has changed so that Trichop
hyton tonsurans now predominates over Microsporum audouinii. With this tran
sition the utility of the Wood's light for diagnosis has been reduced since
T. tonsurans infection is Wood's light negative. Griseofulvin has been the
mainstay of therapy for the last 40 years. The newer antifungal agents-itr
aconazole, terbinafine, and fluconazole-appear to be effective and safe for
the treatment of tinea capitis. When tinea capitis is due to T. tonsurans
or other endothrix species the following regimens have been used: itraconaz
ole continuous regimen (5 mg/kg/day for 4 weeks), itraconazole pulse regime
n with capsules (5 mg/kg/day for 1 week plus 1-3 pulses 3 weeks apart), and
itraconazole pulse regimen with oral solution (3 mg/kg/day for 1 week plus
1-3 pulses 3 weeks apart). With terbinafine tablets the continuous regimen
(>40 kg body weight, 250 mg/day; 20-40 kg, 125 mg/day; and <20 kg, 125 mg/
day) is given for 2 to 4 weeks. Fluconazole tablets or oral suspension (6 m
g/kg/day) were administered for 20 days in one trial. Another possibility m
ay be 6 mg/kg/day for 2 weeks and evaluating the scalp 4 weeks later. An ex
tra week of therapy (6 mg/kg/day) can be administered if clinically indicat
ed at that time, A once-weekly regimen may also be effective. When ectothri
x organisms (e.g., Microsporum canis) are present, a longer duration of the
rapy may be required. The data suggest that the newer agents are effective,
safe with few adverse effects, and have a high benefit:risk ratio. It rema
ins to be seen to what extent griseofulvin will be superseded for the treat
ment of tinea capitis, Adjunctive therapies may help decrease the risk of i
nfection to other individuals. Appropriate measures should be taken to redu
ce the possibility of reinfection.