Research Article |
Open Access |
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Tinea Versicolor - An Epidemiology |
Mahendra Kumar Rai , Sonali Wankhade * |
Department of Biotechnology, SGB Amravati University, Amravati 444 602, Maharashtra, India |
| *Corresponding author: |
Dr. Sonali Wankhade,
Department of Biotechnology,
SGB Amravati University, Amravati 444 602,
Maharashtra, India,
E-mail: sonaliwankhade@rediffmail.com
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Received December 07, 2009; Accepted December 24, 2009; Published December 24, 2009 |
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Citation: Rai MK, Wankhade S (2009) Tinea Versicolor - An Epidemiology. J Microbial Biochem Technol 1: 051-056. doi:10.4172/1948- 5948.1000010 |
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Copyright: © 2009 Rai MK, et al. This is an open-access article distributed
under the terms of the Creative Commons Attribution License,which
permits unrestricted use, distribution, and reproduction in any medium,
provided the original author and source are credited. |
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| Dermatophytic infections have been one of the major
crises prevalent all over the world. Dermatophytes feed
on skin, hair and nail thus causes infection, popularly
known as ‘Tinea infections’. Due to yeast Malassezia furfur
multihued patches occurs on skin and causes infection
known as Tinea versicolor (T.versicolor), which worsens
if neglected. It has global occurrence and is prominent in
hot and humid region. It predominantly affects late teens
and young adults of both sexes. Customarily Tinea versicolor,
is treated by systemic drugs in oral as well as topical
mode. Despite adequate remedy, recurrence is common
with major side effects. For overcoming adverse consequences,
need arises to go naturewide and seek the solution
through herbs. With the help of essential oils, this
stubborn infection can be eradicated effectively, averting
the side effects. |
Keywords |
| Tinea versicolor; Dermatophytes; Malassezia furfur;
Essential oils |
Introduction |
| Tinea versicolor (pityriasis versicolor or PV) is a superficial
fungal infection, characterized by changes in skin pigment due
to colonization of the stratum corneum by a dimorphic lipophilic
fungus of the normal flora of the skin, known as Malassezia furfur
(Adamski, 1995; Sunenshine et al., 1998b; Zaitz et al., 2000;
Moniri et al., 2009). The organism’s yeast phase shows two
morphologically distinct forms, one ovoid, the other spherical,
in which the fungus is named Pityrosporum ovale and
Pityrosporum orbiculare respectively. PV is also known as tinea
versicolor, dermatomycosis furfuracea and tinea flava. Although
it may be distributed globally, it is more commonly found in the
tropics. Often considered a post-pubescent disease, evidence
shows that PV is common in children (Sunenshine et al., 1998b). |
Historical considerations |
| T. versicolor was first recognised as a fungal disease by
Eichsedt in 1846 (Ashbee and Evans, 2002). In 1853, Robin
described the fungus in scales, naming it Microsporum furfur
(Gordon, 1951a). In 1853, Malassez observed “spores” (Gordon,
1951b). Baillon, (1889) used the name Malassezia furfur
in his text to commemorate Malassez (Ashbee et al., 2002). The
genus name Pityrosporum was proposed by Sabouraud in 1904
(Inamadar and Palit, 2003) that were then named Pityrosporum
ovale by Castellani and Chalmers in 1913 (Gupta et al., 2002).
In 1951, Gordon isolated other yeast, micromorphologically distinct
from P. ovale, and named it Pityrosporum orbiculare (Gordon,
1951a; Adamski, 1995; Sunenshine et al., 1998b; Zaitz et al.,
2000; Ashbee et al., 2002). Clinico-epidermiological studies on
T. versicolor were done by Rao et al. (2002). |
Background |
| The lipophilic yeasts are associated with various human diseases,
especially pityriasis versicolor, a chronic superficial scaling
dermatomycosis (Gupta et al., 2002). High temperatures and
humidity favour the occurrence of pityriasis versicolor
(Muhammad et al., 2009). Accordingly, tropical areas can have
prevalence as high as 40% and the frequency is higher during
summer months in temperate climates (Sunenshine et al., 1998a). |
Multiple macules and/or patches of variable appearance
(hypopigmented, hyperpigmented, dark brown or erythematous)
surrounded by normal skin are the typical lesions of pityriasis
versicolor. Affected areas include the back, chest, abdomen, neck,
and upper limbs. However, classically the back carries more lesions.
The face is an area commonly affected in children and it is
the forehead showing mostly hypopigmented macules (Terragni
et al., 1991). Uncommon but possible locations include axilla,
popliteal fossa, fore arms, lower limbs and penis/genitalia
(Terragni et al., 1991; Sunenshine et al., 1998a; Sunenshine et
al., 1998b; Moniri et al., 2009). Although PV had been described
at the beginning of nineteenth century (Ashbee et al., 2002), until
recently classification of its etiologic agent was a matter of doubt.
This controversy may be caused by various morphological features
and fastidious growth requirements of Malassezia yeasts
in vivo. |
Modes of infection |
| Tinea versicolor occur worldwide more frequently in areas
with higher temperatures and higher relative humidities
(Maheswari, 1978; Mellen et al., 2004). |
Although pityriasis versicolor has worldwide occurrence, its
frequency is variable and depends on different climatic, occupational
and socio-economic conditions (Borelli et al., 1991;
Sunenshine et al., 1998a). This disease is prevalent in Iran, in
which almost 6% of all dermatosis and approximately 30% of
dermatomycoses are due to these lipophilic yeasts (Borelli et
al., 1991). Hereditary factor play the role in transmission of the
disease (Maheswari, 1978; Sunenshine et al., 1998b). |
Causal agent |
| • |
M. furfur is now the most commonly accepted name for the
organism causing tinea versicolor. Thus, P. orbiculare, P.
ovale and M. ovalis are synonyms for M. furfur. |
| • |
Despite disagreement about the names, tinea versicolor results
from a shift in the relationship between a human and a
resident yeast flora. |
|
Yeasts of the genus Malassezia are known to be members of
the skin microflora of human and other warm-blooded vertebrates
(Leeming et al., 1989; Moniri et al., 2009). These lipophilic
yeasts are associated with various human diseases, especially
pityriasis versicolor, a chronic superficial scaling dermatomycosis
(Gupta et al., 2002). The genus of Malassezia has undergone
several taxonomic revisions (Ingham and Cunningham,
1993). Later, Gueho et al. (1996) discovered that there were
indeed multiple species which they reclassified and named the
genus as Malassezia with several distinct species. Currently there
are 11 recognised species viz, (1) M. furfur, (Crespo-Erchiga
and Florencio, 2006; Krisanty et al., 2009), (2) M. pachydermatis, (3) M. sympodialis (Makimura et al., 2000; Arzumanian, 2001;
Crespo et al., 2006), (4) M. globosa (Nakabayashi et al., 2000;
Aspiroz et al., 2002; Dutta et al., 2002; Crespo et al., 2000; Crespo
et al., 2006; Moniri et al., 2009), (5) M. obtusa, (6) M. restricta,
(7) M. slooffiae (Gueho et al., 1996), (8) M. dermatis, (9) M.
equi (10) M. nana (Sugita et al., 2002; Hirai et al., 2004) and
(11) M. japonica (Sugita et al., 2005). |
Mortality, race, sex and age |
| Morbidity results primarily from the discolouration. The adverse
cosmetic effect of lesions may lead to significant emotional
distress, particularly in adolescents. Tinea versicolor frequently recurs despite adequate initial therapy. Even with adequate
therapy, residual pigmentary changes may take several
weeks to resolve. Although tinea versicolor usually is more apparent
in darker-skinned individuals, the incidence of tinea versicolor
appears to be the same in all races. |
The role of sex in propensity to development of T.versicolor
is still unclear. Some studies found that PV is more common in
men than women (Belec et al., 1991; Nakabayashi et al., 2000;
Muhammad et al., 2009), while others indicated that the incidence
of this infection is higher in women (Nikpoor and Leppard,
1978). No differences in development of PV among both sexes
are also reported (Belec et al., 1991; Nakabayashi et al., 2000;
Gupta et al., 2002). |
T. versicolor becomes more noticeable with a suntan and is
more common in teenagers and young adults than in older people
(Lesher et al., 1994). However, children are not excluded from suffering
this fungal infection (Terragni et al., 1991; Elewski, 1996;
Gupta et al., 2002; Jena et al., 2005). Similar to other investigations
the highest prevalence of PV was observed in 20-30 yearold
group, suggesting that the peak of the infection is coincided
with ages when the sebum production is in the highest level
(Crespo et al., 2000; Gupta et al., 2002; Moniri et al., 2009).
Very few cases of PV in a child with the age less than 10 years
are found. Moreover, it is rarely seen in older adults (Bhargava
et al., 1997; Rajashekhar, 1997). |
Clinical symptoms |
| The main symptom is persistent patches of discolored skin
with sharp borders (edges) and fine scales. The patches are often
dark reddish-tan in color. Affected areas do not darken in the
sun (skin may appear lighter than surrounding healthy skin): |
| » |
Increased sweating |
| » |
Itching |
|
Physical symptoms |
Lesion characteristics |
| º |
Lesions occur in a variety of colors and shapes, as the name
implies (versi means several). |
| º |
Lesions are either macules or very superficial papules with
fine scale that may not be evident except on close examination. |
| º |
Even when scale is not apparent, when the skin is wiped with
a wet cloth and scraped for examination, it will yield a surprising
amount of dirty brown keratin. If not, the areas of
dyschromia may represent residual effects of previously
treated T. versicolor. |
| º |
Occasionally, it is difficult to determine whether the lighter
or darker skin is affected. |
| º |
Lesions have relatively sharp margins and may be lighter or
darker than the normal skin color. The lesions are frequently
a light orange or tan color in light-skinned individuals. |
| º |
Small lesions are usually circular or oval. |
| º |
Lesions are usually asymptomatic but may be mildly pruritic.
The pruritus is more intense when the patient is excessively
warm. |
| º |
Residual hypopigmentation, without overlying scale, may
remain for many months following effective treatment. These
areas may become more apparent following sun exposure,
causing the patient to suspect incorrectly that the infection
has recurred. |
|
Lesion distribution |
| º |
The upper trunk is affected most commonly, but spread to
the upper arms, antecubital fossae, neck, abdomen, and
popliteal fossae often occur. |
| º |
Lesions in the axillae, groin, thighs, and genitalia may occur
but are less common. |
| º |
Facial, scalp, and palmar lesions occur in the tropics but rarely
in temperate zones. |
| º |
In some patients, T. versicolor primarily affects the flexural
regions, the face, or isolated areas of the extremities. This
unusual pattern of T. versicolor is seen more often in
immunocompromised hosts and can be confused with candidiasis,
seborrheic dermatitis, psoriasis, erythema or dermatophyte
infections. |
| º |
Lesions that are imperceptible or doubtful are more visible
using a wood lamp in a darkened room. |
|
Treatment |
| Questioning the patient about skin or systemic diseases, current
therapy and drug allergies provides guidance in selecting an
appropriate therapy (Okuda et al., 1998; Crowson and Magro,
2003). Topical therapy alone is indicated for most patients (Gupta
et al., 1998; Gupta et al., 2004b; Gupta and Kohli, 2003b). Systemic
treatment is indicated with extensive involvement, recurrent infections or when topical therapy has failed (Gupta et al.,
2003a). Because treatment is relatively easy and recurrence is
common, it is imperative that therapy be as safe, inexpensive
and convenient as possible. A plan for prophylactic therapy should
be discussed with all patients to reduce the high rate of recurrence
(Drake et al., 1996; Gupta et al., 2004a). |
Topical medication |
| º |
Effective topical agents include selenium sulfide (eg, Selsun
shampoo), azole antimycotics, ciclopirox olamine, piroctoneolamine,
zinc pyrithione, propylene glycol lotions, lamisil
derm gel (Faergemann et al., 1997), benzoyl peroxide, sodium
sulfacetamide and allylamine antifungals (Vermeer and
Staats, 1997). Treatment with selenium sulfide may result in
irritant dermatitis. Patients may require emollient or mild
topical steroid application for a few days following therapy |
| º |
The topical azole antifungals work well, but no significant
difference in results is achieved by different compounds.
Topical azole and allylamine antifungals are applied every
other night for 2 weeks. The weekly applications of any of
the topical agents for the following few months may help
prevent recurrence. The main problem with the use of azole
antifungals in T. versicolor is the inconvenience of applying
creams to a wide body surface area. The shampoo form of
the antifungal can be used for extensive disease. |
|
Drug category |
| Topical selenium sulfide products - Selenium sulfide inhibits
M. furfur, the primary cause of T. versicolor. Selenium sulfide
has cytostatic effect on epidermis and follicular epithelium, which
reduces corneocyte production. |
Selenium sulfide (Selsun Blue, Exsel, Head and Shoulders) -
Available as shampoo or lotion in 1% or 2.5% concentrations. It
is a safe and effective therapy that has been used for years
(Albright and Hitch, 1966; Bamford, 1983; Katsambas et al.,
1996; Hull and Johnson, 2004). However, it is an irritant, and
some patients complain of itching or eczema after overnight
applications. It also may stain clothes and bedding. Lotion is not
preferred in children and patients with sensitive skin. |
Over the conter and prescription creams |
| Products include clotrimazole (Lotrimin-AF) and ketoconazole
(Nizoral) creams. Prescription alternatives for T. versicolor include
ketoconazole (Nizoral shampoo), ciclopirox (Loprox),
butenafine (Mentax), naftifine (Naftin) (Meinicke et al., 1984),
econazole (Spectazole), oxiconazole (Oxistat) and sulconazole
(Exelderm). |
Oral medication |
| Some patients prefer oral therapy. It is recommended to take
the oral drug with an acidic drink (e.g. orange juice, Coke) to
improve absorption may enhance this therapy. Next, the patient
should wait an hour and then exercise to the point of sweating.
The patient then cools off, allowing the perspiration to dry on
the skin, and showers after a few hours. |
Oral therapy does not prevent the high rate of recurrence, and
treatment with oral ketoconazole may need to be repeated on an
intermittent basis throughout the year (Gan et al., 1987; Hickman,
1996; Fernandez-Torres et al., 2000; Gupta et al., 2003a; Gupta
et al., 2003b; Rincon et al., 2006). Oral itraconazole and
fluconazole also have been proven effective (Faergemann, 1992;
Gupta et al., 1994; Kose, 1995; Leyden, 1998; Balachandran et
al., 1999; Fernandez-Torres et al., 2000; Matar et al., 2003; Partap
et al., 2004; Karakas et al., 2005) but rarely are required. Some
sub-groups of M. furfur apparently are not clinically responsive to oral terbinafine (Tosti et al., 1996; Leeming et al., 1997; Fernandez-
Torres et al., 2000). Griseofulvin is not an effective therapy for
T. versicolor. |
Ketoconazole (Nizoral) |
| A single dose of oral ketoconazole (400 mg) is very effective
(Fernandez-Nava et al., 1997). Imidazole broad-spectrum antifungal
agent; inhibits synthesis of ergosterol, causing cellular
components to leak, resulting in fungal cell death. This drug
achieves excellent skin levels with minimal dosing. M furfur is
eradicated by the presence of ketoconazole in the outer skin layers
(Rausch et al., 1984; Gan et al., 1987; Hickman, 1996). Children
less than 10 year are not being treated with oral ketoconazole. |
Combination |
| Various regimens use both topical and oral therapies. The most
common is varying regimens of selenium sulfide shampoo or
lotion and oral therapy with ketoconazole (Rausch et al., 1984). |
Disadvantages |
Disadvantages of topical treatment |
| Although topical drugs can provide immediate reductions in
infectivity, are free of systemic adverse effects. These drugs have
some disadvantages e.g. the time needed and difficult application
of the drug over large affected areas, especially on the trunk,
can not use in broken/open skin as well as the unpleasant odour
of certain agents. For these reasons, patient adhesion is inadequate,
which increases the rate of recurrence. Effectiveness of
topical agents is lower, and rate of recurrence varies form 60 to
80% (Savin, 1996). It is found difficult to continue treatment or
to know where to apply the cream, once the inflammatory signs
have settled. Topical drugs may be difficult to use in certain areas
e.g. on the hair, nails, nipples and in some more sensitive
areas. Along with this some adverse reactions are most common
such as increase in hypersensitivity and irritation occurs, mild
dryness of the skin and itching etc. (Gupta and Summerbell,
2000). |
Disadvantages of oral drugs |
| Drugs taken orally affect both diseased and normal tissues,
thus increasing the chance of side effects. Inspite of short term
treatment they bring lot of side effects. Shows hypersensitivity,
not recommended for children, nausea, headache, vomiting.
Hepatotoxicity may be associated with some oral antifugal medications
(Sunenshine et al., 1998b). Conventional skin disease treatments
such as the drugs ketoconazole, ciclopirox, naftifine and
tolnaftate can irritate the skin, causing stinging, itching, redness,
drying or allergic reactions (Gupta et al., 1998; Gupta and
Summerbell, 2000). |
Prevention |
| • |
T. versicolor has a high rate of recurrence and may require
frequent prophylactic treatment with topical or oral therapy
on an intermittent basis. |
| • |
Good personal hygiene may be helpful in limiting recurrences.
Specifically, patients should shower as soon as possible after
participating in activities or exercise that produce significant
perspiration. |
|
Medical/legal pitfalls |
| • |
Routine evaluation of hepatic function before therapy is seldom
warranted for young healthy patients. However, patients
at extra risk for preexisting hepatic dysfunction need assessment
before treatment. Hepatotoxicity has been associated
with the use of ketoconazole tablets, including rare fatalities.
Several cases of hepatitis have been reported in children. |
| • |
In patients taking terbenafine concurrently with ketoconazole
tablets and other serious ventricular dysrhythmias (in rare
cases, leading to fatality) have been recorded. |
| • |
Pharmacokinetic data indicate that oral ketoconazole inhibits
the metabolism of astemizole, resulting in elevated plasma
levels of astemizole and i ts act ive metabolite desmethylastemizole, which may prolong QT intervals. |
| • |
Ketoconazole may enhance the anticoagulant effect of coumarin
like drugs. |
|
Future aspect |
| The existing treatments have lot of limitations and hence prove
to be less effective. The factors contributing to its ineffectiveness
are lengthy treatment, costly drugs and sometimes inability
to cure the disease. This spawns the need of deriving an appropriate
technology. The stepwise study is to be carried out in which
foremost thing is the proper diagonosis. Effects of essential oils
of various herbs are to be categorically studied on various factors
such as sex, age, group, natural inhabitants, geographical
conditions etc. Pathogenicity of dermatophytes is also to be studied.
The above factors need a concurrent study and reasons for
infections, remedies and effectiveness of the drugs are to be evaluated. |
Now a day the importance of herbal drugs is reinstated and the
world is turning towards safer drugs with no side effects. Thus
the exploration of newer drugs from plants is most sought after,
which will prove to be cheaper, safer and more effective. Historically,
essential oils have been used for therapeutic purposes.
In recent years, much research has been devoted to investigate
such plant extracts, their active components, modes of action
and synergistic effects with other antimicrobial compounds (Baris
et al., 2006; Chuang et al., 2007; Zilda et al., 2008; Santos et al.,
2008; Ademar et al., 2008; Barrera et al., 2009; Mahboubi and
Kazempour, 2009; Mahboubia et al., 2009). These findings of
researchers stimulate to explore other plant products, which could
be exploited as effective antifungal, especially against
T.Versicolor. |
Conclusion |
| Tinea infection is an obstinate disease which bothered dermatologists
a lot. The prime task of dermatologist is to precisely
diagnose the underlying agent causing the disease. Once this is
done, selection of a most favorable antifungal drug can be carried
out effectively. Its spectrum of activity which covers the
infecting microorganism can prove to be a potent treatment. Last
decade showed some noteworthy progress in the evolution of
effective and safe drugs for T. versicolor, but could not fulfill
the expectations due to their negative aspects such as adverse
reactions, expensiveness and lengthy treatment. Effective therapy
demands oral suspension along with the topical drugs. But benefits
of these drugs are outshined by the fact that they are having a lot of side effects, such as nausea, headache, vomiting, while
less common adverse reactions are abdominal discomfort, transient
rash, urticaria, diarrhea and photosensitivity etc. |
Diagnostic methodology and fungal susceptibility testing lag
behind therapeutic advances. We should turn our attention to these
problems by seeking the solutions through the essential oils of
medicinal plants. Essential oils are the rich resource of drugs for
traditional, folk, synthetic and modern medicines; nutraceuticals
and food supplements. Due to presence of numerous chemical
compounds, plants of this family possess biological activity including
antibacterial, antiviral, antifungal and anti-inflammatory. |
References |
- Adamski Z (1995) Studies of a role played by lipophilic yeasts Malassezia
furfur (Pityrosporum ovale, Pityrosporum orbiculare) in different dermatoses.
Postepy Dermatol 12: 349-454.
- Ademar A, Joao PB, Sandra S, Niege AJ, Marcio LA, et al. (2008) Antimicrobial
Activity of the Extract and Isolated Compounds from Baccharis
dracunculifolia D.C. (Asteraceae). Naturforsch 63: 40-46. » CrossRef » Google Scholar
- Albright SD III, Hitch JM (1966) Rapid treatment of tinea versicolor with
selenium sulfide. Arch Dermatol 93: 460-462. » CrossRef » PubMed » Google Scholar
- Arzumanian VG (2001) The yeast Malassezia on the skin of healthy individuals
and patients with atopic dermatitis. Vestn Ross Akad Med Nauk 2:
29-31. » PubMed » Google Scholar
- Ashbee HR, Evans EG (2002) Immunology of Diseases Associated with
Malassezia Species. Clin Microbiol Rev 15: 21-57. » CrossRef » PubMed » Google Scholar
- Aspiroz C, Ara M, Varea M, Rezusta A, Rubio C (2002) Isolation of
Malassezia globosa and M. sympodialis from patients with pityriasis versicolor
in Spain. Mycopathologia 154: 111-117. » CrossRef » PubMed » Google Scholar
- Balachandran C, Thajuddin BC, Ravikumar BC (1999) Comparative evaluation
of single dose regimen with two dose regimen of fluconazole in the
treatment of tinea versicolor: A double blind placebo controlled study. Indian
J Dermatol Venereol Leprol 65: 20-22.
- Bamford JT (1983) Treatment of tinea versicolor with sulfur-salicylic shampoo.
J Am Acad Dermatol 8: 211-213. » PubMed » Google Scholar
- Baris O, Gulluce M, Sahin F, Ozer H, Kilic H, et al. (2006) Biological
activities of the essential oil and methanol extract of Achillea Biebersteinii
Afan. (Asteraceae) Turk J Biol 30: 65-73.
- Barrera-Necha LL, Garduno-Pizana C, Garcia-Barrera LJ (2009) In vitro
antifungal activity of essential oils and their compounds on Mycelial growth
of Fusarium oxysporum f. sp. gladioli (Massey) Snyder and Hansen. Plant
Pathology Journal 8: 17-21. » CrossRef » Google Scholar
- Belec L, Testa J, Bouree P (1991) Pityriasis versicolor in the Central African
Republic: a randomized study of 144 cases. J Med Vet Mycol 29: 323-
329. » PubMed » Google Scholar
- Bhargava P, Kuldeep CM, Mathur NK (1997) Tinea versicolor localized to
dorsal surface of hands and feet - A rare presentation in childhood. Indian J
Dermatol Venereol Leprol 63: 382-383.» CrossRef » Google Scholar
- Borelli D, Jacobs PH, Nall L (1991) Tinea versicolor: epidemiologic, clinical
and therapeutic aspects. J Am Acad Dermatol 25: 300-305. » CrossRef » PubMed » Google Scholar
- Chuang PH, Lee CW, Chou JY, Murugan M, Shieh BJ, et al. (2007) Antifungal
activity of crude extracts and essential oil of Moringa oleifera Lam.
Bioresour Technol 98: 232-236. » CrossRef » PubMed » Google Scholar
- De Araújo AA, Santana MHA (1996) Aerobic immobilized cells in alginate
gel particles of variable density. Appl Biochem Biotech 57/58: 543-550. » CrossRef » Google Scholar
- Crespo-Erchiga V, Florencio VD (2006) Malassezia yeasts and pityriasis
versicolor. Curr Opin Infect Dis 19: 139-147. » PubMed » Google Scholar
- Crowson AN, Magro CM (2003) Atrophying tinea versicolor: a clinical and
histological study of 12 patients. Int J Dermatol 42: 928-932. » CrossRef » PubMed » Google Scholar
- Drake LA, Dinehart SM, Farmer ER, Goltz RW, Graham GF, et al. (1996)
Guidelines of care for superficial mycotic infections of the skin: tinea infections.
J Am Acad Dermatol 34: 282-286. » CrossRef » Google Scholar
- Dutta S, Bajaj AK, Basu S, Dikshit A (2002) Pityriasis versicolor: socioeconomic
and clinico-mycologic study in India. Int J Dermatol 41: 823-824. » CrossRef » PubMed » Google Scholar
- Elewski BE (1996) Cutaneous mycoses in children. Br J Dermatol 134: 7-
11. » CrossRef » PubMed » Google Scholar
- Faergemann J (1992) Treatment of pityriasis versicolor with a single dose
of fluconazole. Acta Derm Venereol 72: 74-75. » PubMed » Google Scholar
- Faergemann J, Hersle K, Nordin P (1997) Pityriasis versicolor: clinical experience
with Lamisil cream and Lamisil DermGel. Dermatology 194: 19-
21.» CrossRef » PubMed » Google Scholar
- Fernandez-Nava HD, Laya-Cuadra B, Tianco EA (1997) Comparison of
single dose 400 mg versus 10-day 200 mg daily dose ketoconazole in the
treatment of tinea versicolor. Int J Dermatol 36: 64-66. » PubMed » Google Scholar
- Fernandez-Torres B, Va´zquez-Veiga H, Llovo X, Pereiro M Jr, Guarro J
(2000) In vitro susceptibility to itraconazole, clotrimazole, ketoconazole,
and terbinafine of 100 isolates of Trichophyton rubrum. Chemotherapy 46:
390-394. » CrossRef » PubMed » Google Scholar
- Gan VN, Petruska M, Ginsburg CM (1987) Epidemiology and treatment of
tinea capitis: Ketoconazole v/s griseofulvin. Pedtr Infect Dis J 6: 46-49. » CrossRef » Google Scholar
- Gordon MA (1951a) Lipophilic yeast like organisms associated with tinea
versicolor. J Invest Dermatol 17: 267-272. » Google Scholar
- Gordon MA (1951b) The lipophilic mycoflora of the skin. Mycologia 43:
524-534. » Google Scholar
- Gueho E, Midgley G, Guillot J (1996) The genus Malassezia with description
of four new species. Antonie van Leeuwenhoek 69: 337-355.» CrossRef » PubMed » Google Scholar
- Gupta AK, Sauder DN, Shear NH (1994) Antifungal agents: An overview.
Part I. J Am Acad Dermatol 30: 677-698. » Google Scholar
- Gupta AK, Einarson TR, Summerbell RC (1998) An overview of topical
antifungal therapy in dermatomycoses. A North American Perspective Drug
55: 645-675. » CrossRef» PubMed » Google Scholar
- Gupta AK, Summerbell RC (2000) Tinea capitis. Medical Mycology 38:
255-287. » CrossRef » PubMed » Google Scholar
- Gupta AK, Bluhm R, Summerbell R (2002) Pityriasis versicolor. J Eur Acad
Dermatol Venereol 16: 19-33. » CrossRef » PubMed
- Gupta AK, Batra R, Bluhm R, Faergemann J (2003a) Pityriasis versicolor.
Dermatol Clin 21: 413-429. » PubMed » Google Scholar
- Gupta AK, Kohli Y (2003b) In vitro susceptibility testing of ciclopirox,
terbinafine, ketoconazole and itraconazole against dermatophytes and
nondermatophytes and in-vitro evaluation of combination antifungal activity.
Br J Dermatol 149: 296-305. » CrossRef » PubMed » Google Scholar
- Gupta AK, Cooper EA, Ryder JE, Nicol KA, Chow M, et al. (2004a) Optimal
management of fungal infections of the skin, hair, and nails. Am J Clin
Dermatol 5: 225-237. » CrossRef » PubMed » Google Scholar
- Gupta AK, Batra R, Bluhm R, Boekhout T, Dawson TL Jr (2004b) Skin
diseases associated with Malassezia species. J Am Acad Dermatol 51: 785-
798. » CrossRef » PubMed » Google Scholar
- Hickman JG (1996) A double-blind, randomized, placebo-controlled evaluation of short-term treatment with oral itraconazole in patients with tinea
versicolor. J Am Acad Dermatol 34: 785- 787. » CrossRef » PubMed » Google Scholar
- Hirai A, Kano R, Makimura K, Duarte ER, Hamdan JS, et al. (2004)
Malassezia nana sp. Nov., a novel lipid-dependent yeast species isolated
from animals. Int J Syst Evol Microbiol 54: 623- 627. » CrossRef » PubMed » Google Scholar
- Hull CA, Johnson SM (2004) A double-blind comparative study of sodium
sulfacetamide lotion 10% versus selenium sulfide lotion 2.5% in the treatment
of pityriasis (tinea) versicolor. Cutis 73: 425-429. » PubMed » Google Scholar
- Inamadar AC, Palit A (2003) The genus Malassezia and human disease.
Indian J Dermatol Venereol Leprol 69: 265-270. » CrossRef » PubMed » Google Scholar
- Ingham E, Cunningham AC (1993) Malassezia furfur. Med Mycol 31: 265-
288. » CrossRef » Google Scholar
- Jena DK, Sengupta S, Dwari BC, Ram MK (2005) Pityriasis versicolor in
the pediatric age group. Indian J Dermatol Venereol Leprol 71: 259-261. » CrossRef » PubMed » Google Scholar
- Karakas M, Durdu M, Memisoglu HR (2005) Oral fluconazole in the treatment
of tinea versicolor. J Dermatol 32: 19-21. » PubMed » Google Scholar
- Katsambas A, Rigopoulos D, Antoniou C (1996) Econazole 1% shampoo
versus selenium in the treatment of tinea versicolor: a single-blind randomized
clinical study. Int J Dermatol 35: 667- 668. » CrossRef » PubMed » Google Scholar
- Kose O (1995) Fluconazole versus itraconazole in the treatment of tinea
versicolor. Int J Dermatol 34: 498-499. » PubMed » Google Scholar
- Krisanty RI, Bramono K, Made WI (2009) Identification of Malassezia species
from pityriasis versicolor in Indonesia and its relationship with clinical
characteristics. Mycoses 52: 257-62. » CrossRef » PubMed » Google Scholar
- Leeming JP, Sansom JE, Burton JL (1997) Susceptibility of Malassezia
furfur subgroups to terbinafine. Br J Dermatol 137: 764-767. » CrossRef » PubMed » Google Scholar
- Leeming JP, Notman FH, Holland KT (1989) The distribution and ecology
of Malassezia furfur and cutaneous bacteria on human skin. J Appl Bacteriol
67: 47-52.» CrossRef » PubMed » Google Scholar
- Lesher J, N Levine, P Treadwell (1994) Fungal skin infections: common but stubborn. Patient Care
28: 16-31.
- Leyden J (1998) Pharmacokinetics and pharmacology of terbinafine and
itraconazole. J Am Acad Dermatol 38: S42-47. » CrossRef » PubMed » Google Scholar
- Mahboubi M, Kazempour N (2009) The antimicrobial activity of essential
oil from Perovskia abrotanoides karel and its main components. Indian J
Pharm Sci 71: 343-347. » CrossRef » Google Scholar
- Mahboubia M, Feizabadib MM, Safarab M (2008) Antifungal activity of
essential oils from Zataria multiflora, Rosmarinus officinalis, Lavandula
stoechas, Artemisia sieberi Besser and Pelargonium graveolens against clinical
isolates of Candida albicanS. Pharmacognosy Magazine 4: 15-18. » Google Scholar
- Maheswari AS (1978) Clinical and epidemiological studies on tinea versicolor
in Kerala. Indian J Dermatol Venereal Leprol 44: 345. » CrossRef » Google Scholar
- Makimura K, Tamura Y, Kudo M, Uchida K, Saito H, et al. (2000) Species identification and strain
typing of Malassezia species stock strains and clinical isolates based on the
DNA sequences of nuclear ribosomal internal transcribed spacer 1 regions.
J Med Microbiol 49: 29-35. » CrossRef » PubMed » Google Scholar
- Matar MJ, Ostrosky-Zeichner L, Paetznick VL, Rodriguez JR, Chen E, et
al. (2003) Correlation between E-test, disk diffusion, and microdilution
methods for antifungal susceptibility testing of fluconazole and voriconazole.
Antimicrob. Agents Chemother 47: 1647-1651. » CrossRef » PubMed » Google Scholar
- Meinicke K, Striegel C, Weidinger G (1984) Treatment of dermatomycoses
with naftin. Therapeutic effectiveness following once and twice daily
administration. Mycosen 27: 608- 614. » PubMed » Google Scholar
- Mellen LA, Vallee J, Feldman SR (2004) Treatment of pityriasis versicolor
in the United States. J Dermatolog Treat 15: 189-192. » CrossRef » PubMed » Google Scholar
- Moniri R, Nazeri M, Amiri S, Asghari B (2009) Isolation and identification
of Malassezia spp. In pytiriasis versicolor in Kashan, Iran. Pak J Med Sci
25: 837-840. » CrossRef » Google Scholar
- Muhammad N, Kamal M, Islam T, Islam N, Shafiquzzaman M (2009) A
study to evaluate the efficacy and safety of oral fluconazole in the treatment
of tinea versicolor. Mymensingh Med J 18: 31-35. » PubMed » Google Scholar
- Nakabayashi A, Sei Y, Guillot J (2000) Identification of Malassezia species
isolated from patients with seborrhoeic dermatitis, atopic dermatitis, pityriasis
versicolor and normal subjects. Med Mycol 38: 337-341.» CrossRef » PubMed » Google Scholar
- Nikpoor N, Leppard B (1978) Fungal disease in Shiraz. Pahlavi Med J 9:
27-49. » PubMed » Google Scholar
- Okuda C, Ito M, Naka W, Nishikawa T, Tanuma H, et al. (1998) Pityriasis
versicolor with a unique clinical appearance. Med Mycol 36: 331-334. » CrossRef » PubMed » Google Scholar
- Partap R, Kaur I, Chakrabarti A, kumar B (2004) Single-dose fluconazole versus
itraconazole in pityriasis versicolor. Dermatology 208: 55-59. » CrossRef » PubMed » Google Scholar
- Rajashekhar N (1997) Oral fluconazole in tinea versicolor. Indian J Dermatol
Venereol Leprol 63: 166-167. » Google Scholar
- Rao GS, Kuruvilla M, Kumar P, Vinod V (2002) Clinico-epidermiological
studies on tinea versicolor. Indian J Dermatol Venereol Leprol 68: 208-209. » CrossRef » PubMed » Google Scholar
- Rausch LJ, Jacobs PH (1984) Tinea versicolor: treatment and prophylaxis
with monthly administration of ketoconazole. Cutis 34: 470-471. » PubMed » Google Scholar
- Rincon S, Cepero de Garcýa MC, Espinel-Ingroff A (2006) A Modified
Christensen’s Urea and CLSI Broth Microdilution Method for Testing
Susceptibilities of Six Malassezia Species to Voriconazole, Itraconazole,
and Ketoconazole. J Clin Microbiol 44: 3429-3431. » CrossRef » PubMed » Google Scholar
- Santos AO, Ueda-Nakamura T, Dias Filho BP (2008) Antimicrobial activity
of Brazilian copaiba oils obtained from different species of the Copaifera
genus. Mem Inst Oswaldo Cruz Maio 103: 277-281. » CrossRef » PubMed » Google Scholar
- Savin R (1996) Diagnosis and treatment of tinea versicolor. J Fam Pract 43:
127-132. » PubMed » Google Scholar
- Sugita T, Takashima M, Shinoda T, Suto H, Unno T, et al. (2002) New yeast
species, Malassezia dermatis, isolated from patients with atopic dermatitis.
J Clin Microbiol 40: 1363-1367. » CrossRef » PubMed » Google Scholar
- Sugita T, Tajima M, Ito T, Saito M, Tsuboi R, et al. (2005) Antifungal Activities
of Tacrolimus and Azole Agents against the Eleven Currently Accepted
Malassezia Species. J Clin Microbiol 43: 2824-2829. » CrossRef » PubMed » Google Scholar
- Sunenshine PJ, Schwartz RA, Janniger CK (1998a) Tinea versicolor: an
update. Cutis 61: 65-68, 71-72. » PubMed » Google Scholar
- Sunenshine PJ, Schwartz RA, Janniger CK (1998b) Review. Tinea versicolor.
Int J Dermatol 37: 648-655. » CrossRef » PubMed » Google Scholar
- Tarazooie B, Kordbacheh P, Zaini F, Zomorodian K, Saadat F, et al. (2004)
Study of the distribution of Malassezia species in patients with pityriasis
versicolor and healthy individuals in Tehran, Iran. BMC Dermatol 4: 5. » CrossRef » PubMed » Google Scholar
- Terragni L, Lasagni A, Oriani A, Gelmetti C (1991) Pityriasis versicolor in
the pediatric age. Pediatr Dermatol 8: 9-12. » CrossRef » PubMed » Google Scholar
- Tosti A, Piraccini BM, Stinchi C, Venturo N, Bardazzi F, et al. (1996) Treatment
of dermatophyte nail infections: An open randomized study comparing
intermittent terbinafine therapy with continuous terbinafine treatment
and intermittent itraconazole therapy. J Am Acad Dermatol 34: 595-600. » PubMed » Google Scholar
- Vermeer BJ, Staats C (1997) The efficacy of a topical application of
terbinafine 1% solution in subjects with pityriasis versicolor: a placebocontrolled
study. Dermatology 1: 22-24. » PubMed » Google Scholar
- Zaitz C, LRB Ruiz, VM Souza (2000) Dermatosis associated with yeasts from Malassezia genus.
An Bras Dermatol 75: 129-142. » Google Scholar
- Zilda CG, Claudia MR, Sandra RF, Terezinha IES (2008) Antifungal activity
of the essential oil from Calendula officinalis (Asteraceae) growing in
brazil. Brazilian Journal of Microbiology 39: 61-63. » Google Scholar
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