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Texte intégral de l'article
 
  Version imprimable

Tinea capitis by Trichophyton schöenleinii


European Journal of Dermatology. Volume 11, Numéro 5, 481-2, September - October 2001, Votre diagnostic !


Résumé   Summary  

Auteur(s) : Glória da Cunha Velho, Manuela Selores, Isabel Amorim, Virgínia Lopes, Department of Dermatology, Hospital Geral de Santo António, 4430 VN Gaia, Portugal..

Résumé : A five year-old female orphan, living in an SOS Village, had been treated unsuccessfully for tinea amiantacea with tars and salicilic acid shampoos for two years. She presented with powdery grey hair and large adherent scales surrounding the hair shafts without alopecia (Fig. 1). Wood's lamp examination revealed a yellow fluorescence. She had no skin lesions and was a healthy child. Scales and altered hairs were collected.

Illustrations

ARTICLE

Tinea capitis by Trichophyton schöenleinii

The direct microscopic examination of the scrapings and hair, with lactophenol - blue, showed septate hyaline hyphae and arthrospores with an endothrix parasitism (Fig. 2).

Sabouraud dextrose agar with antibiotics and mycobiotic cultures were incubated at 25º C and 37º C. The cultures showed slow growing waxy colonies with irregular borders that submerged into the agar. The surface of the colonies, at first white, became cream coloured and the reverse was non-pigmented (Fig. 3).

This dermatophyte grew equally at room temperature and at 37º C. The urease test was negative and growth was not enhanced on media enriched with vitamins or aminoacids. Irregular and multiple branched hyphae with broadened tips, or antlerlike structures also known as favic chandeliers were the characteristic features seen (Fig. 4). Chlamydospores were common in older cultures. Neither microconidia nor macroconidia were seen.

A diagnosis of tinea capitis by Trichophyton schöenleinii was made.

She was treated with 15 mg/kg/day of oral micronized griseofulvin (375 mg once a day) and ketoconazole shampoo (once a day) for twelve weeks.

All the household members (a total of ten children and one adult) and our patient's sister, who was visiting her frequently at that time, were screened for the presence of hair and scaling lesions and fluorescence. A total of six samples were collected from the fluorescence positive scalps. We detected T. schöenleinii only in our patient's sister.

Nevertheless, all the children were treated with ketoconazole shampoo (once a day) and her sister was additionally prescribed oral griseofulvin.

Patients were rechecked and cultures obtained, and the child was clinically and mycologically cured. We do not know what happened to her sister since we lost contact.

T. schöenleinii is an important anthropophilic dermatophyte that causes Tinea favosa, a rare and chronic disease characterised by the presence of yellowish, cup-shaped crusts called scutula, on the scalp and glabrous skin [1], and severe alopecia. Besides this classic clinical type there are erythematous follicular forms, without alopecia, similar to seborrheic dermatitis, psoriasis or tinea amiantacea [2, 3]. Because of its non-inflammatory appearance, the disorder may persist for years before it is diagnosed [2].

The peculiar type of hair invasion (endothrix favic) contributes to the chronic course of the favus, which may persist in adult life [4]. Endothrix infections are more likely to result in outbreaks among family members or intimate friends [3]. T. schöenleinii can be transmitted from person to person by sharing towels or clothing [5].

A recent study has revealed that symptomatic children may not be the source of infection of other children [6]. However, it showed that a high percentage of symptom-free adult carriers at home could act as reservoirs of infection [4] and were responsible for the spread and persistence of scalp ringworm in the community [7].

The question of whether asymptomatic carriers should be treated with oral antifungals or antiseborrheic shampoos remains [8]. However, there is a slight risk of adverse reactions from oral griseofulvin administered for 4-6 weeks [4]; the regular use of a shampoo is an appealing solution for controlling the carrier state, particularly in closed institutions. Unfortunately only one controlled study has evaluated treatment options for the carrier state [2, 4, 7, 8].

Although the favus occurred worldwide in the past it is now limited to some endemic regions, probably due to the great improvement of socio-economic conditions [9, 10]. During the past decade, there have been some cases confined to Germany [11], West Iran [12], Jordan [13] and Brazil [14].

Our patient presented a seborrheic-like scaling, without alopecia, resistant to the usual treatment and not suggestive of tinea capitis. We emphasise the importance of microbiological study in such cases.

Her sister was presumably the source of the infection, since the household members who had a positive fluorescence, were not infected and the others had apparently healthy scalps.

In spite of being a rare agent of tinea in Portugal nowadays, T. schöenleinii exists sporadically in endemic areas, which also happens in other countries [9, 10]. As we lost contact with our patient's sister we presume the source may not be totally eradicated.

Article accepted on 30/1/01

REFERENCES

1. Weitzman I, Summerbell RC. The dermatophytes. Cl Microb Rev, 1995: 240-59.

2. Esteves JA, Cabrita JD, Nobre GN. Micologia Médica. Lisboa. Fundação Calouste Gulbenkian. 1990: 447.

3. Frieden IJ, Howard R. Tinea capitis: Epidemiology, diagnosis, treatment, and control. J Am Acad Dermatol 1994; 31: S42-6.

4. Greer DL. Treatment of the symptom-free carriers in the management of tinea capitis. The Lancet 1996; 348: 350-1.

5. Aly R. Ecology, epidemiology and diagnosis of tinea capitis. Pediatr Infect Dis J 1999; 18: 180-5.

6. Williams JV, Honig PJ, McGinley KJ, Leyden JJ. Semiquantitative study of tinea capitis and the asymptomatic carrier state in the inner-city school children. Pediatrics 1995; 96: 265-7.

7. Neil G, Hanslo D, Buccimazza S, Kibel M. Control of the carrier state of the scalp dermatophytes. Pediatric Infect Dis J 1990; 9: 57-8.

8. Vargo K, Cohen BA. Prevalence of undetected tinea capitis in household members of children with disease. Pediatrics 1993; 92: 155-6.

9. Korstanje MJ, Staats CCG. Tinea capitis in Northwestern Europe 1963-1993: etiologic agents and their changing prevalence. Int J Derm 1994; 33: 548-9.

10. Venugopal PV, Venugopal TV. Tinea capitis in Saudi Arabia. Int J Derm 1993; 32: 39-40.

11. Zienicke HC, Korting HC, Lukaes A, Braun-Falco O. Dematophytosis in children and adolescents: epidemiological, clinical, and microbiological aspects changing with age. J Dermatol 1991; 18: 438-46.

12. Omidynia E, et al. A study of dermatophytoses in Hamadan, the governmentship of West Iran. Mycopathologia 1996; 133: 9-13.

13. Abu-Elteen KH, Abdul Malek M. Prevalence of dermatophytoses in the Zarqa district of Jordan. Mycopathologia 1999; 145: 137-42.

14. Belda Junior W, et al. Tinea favosa. Report of a familial occurrence in Itapeceria da Serra. Rev Inst Med Trop São Paulo 1990; 32: 58-62.


 

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