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Dermatophytosis
Ringworm, Tinea,
Last Updated: March 2013
Importance
Dermatophytosis is a common contagious disease caused by fungi known as
dermatophytes. Dermatophytes belong to a group of organisms that are able to break
down the keratin in tissues such as the epidermis, hair, nails, feathers, horns and hooves.
Most of these fungi reside in the soil and are involved in decomposition; however, the
dermatophytes can infect living hosts. Some dermatophytes (anthropophilic species)
are adapted to humans, and are usually transmitted from person to person. Others
(zoophilic species) are adapted to animals. A few (geophilic) species normally live in
the environment, but occasionally act as parasites. The zoophilic and geophilic species
are sometimes transmitted from animals to people. It is also possible for humans to
transmit anthropophilic dermatophytes to animals, although this seems to be
uncommon.
In living hosts, dermatophytes usually remain in superficial tissues such as the
epidermis, hair and nails. Serious consequences are uncommon and infections can be
self-limiting. However, the illness may be disfiguring and uncomfortable, especially
when the lesions are widespread. Economic effects, such as damage to hides, are also
important in livestock. Infrequently, dermatophytes may invade subcutaneous tissues
and (very rarely) other sites, especially in immunocompromised hosts.
Etiology
Dermatophytosis is caused by pathogenic, keratin-digesting fungi in the genera
Microsporum, Trichophyton and Epidermophyton. Members of Microsporum and
Trichophyton cause illness in both humans and animals. E. floccosum is the only species
of Epidermophyton known to cause disease, and it usually affects only people. Some
authors use the term “dermatophytoids” for soil-dwelling members of Microsporum,
Trichophyton and Epidermophyton that are never or rarely associated with disease (e.g.,
T. terrestre).
Dermatophytes, like many fungi, may have two different species names. One name
belongs to the asexual form (the anamorph state), which is the form that occurs in
vertebrate hosts. The other name is given to the sexual state of the organism. The latter
form, called the teleomorph form or the “perfect state,” is produced by mating between
anamorphs. For example, the dermatophyte Microsporum canis infects animals;
however, when this organism mates with a compatible environmental organism, the
resulting sexual form is called Arthroderma otae. The teleomorph (perfect) states of
both Microsporum and Trichophyton belong to the genus Arthroderma, and
dermatophytes known to have sexual states are placed in the phylum Ascomycota,
family Arthrodermataceae. Dermatophytes that currently have no known sexual state,
like other medically important fungi with this characteristic, are classified as
Deuteromycota (Fungi Imperfecti).
Although dermatophytes originated from soil-dwelling keratinophilic organisms,
only a few pathogenic species still reside primarily in this niche. These organisms,
known as geophilic dermatophytes, are associated with decomposing keratin sources in
the environment. M. gypseum and M. nanum are the only two geophilic dermatophytes
that are important pathogens in animals. M. gypseum is also seen in people, but M.
nanum occurs infrequently.
Most species that cause dermatophytosis have become adapted to people or
animals, and are now maintained in these reservoirs. Although they can infect other
hosts, each dermatophyte tends to be associated with a particular host or group of hosts,
and it is not maintained in other species long term. Zoophilic dermatophytes are adapted
to various animal species, while anthropophilic dermatophytes occur in humans.
Zoophilic Microsporum species include Microsporum canis, M. gallinae and M.
persicolor. Most sources no longer use the name M. equinum for the organisms found
in horses, but consider them to be equine-adapted M. canis. Zoophilic members of
Trichophyton include Trichophyton equinum, T. bullosum, members of the T.
mentagrophytes complex, T. simii and T. verrucosum. Most or all zoophilic
dermatophytes are thought to be zoonotic, although some are transferred to people more
often than others.
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There are numerous species of anthropophilic
dermatophytes, including T. tonsurans, the T. rubrum
complex, T. violaceum, T. mentagrophytes var. interdigitale,
T. soudanense, T. schoenleinii, M. audouinii, E. floccosum
and others. Although anthropophilic dermatophytes can be
transmitted to animals, this seems to be rare.
The predominant dermatophytes involved in human
cases vary with the climate, geographic location and other
factors such as exposure to livestock, pets or exotic species.
Zoophilic dermatophytes can be a common cause of a
syndrome in one region, while anthropophilic dermatophytes
account for most cases in another. The causative agents can
also change over time, with some species becoming less
common (e.g., due to the introduction of effective treatments
or changes in exposure) and others becoming more
prevalent.
Dermatophyte taxonomy
The taxonomy of the dermatophytes, particularly
members of T. mentagrophytes, is controversial. Organisms
may be assigned different names depending on whether the
source is using traditional identification methods or genetic
typing.
Diagnostic laboratories have traditionally identified
dermatophytes based on their colony and microscopic
morphology, nutritional and biochemical characteristics, and
other factors. Such methods, together with the ecology of an
organism (e.g., its adaptation to a particular host) have given
rise to a number of species names. However, some organisms
that appear to be different species, based on conventional
typing and/or ecology, may be very closely related
genetically. Furthermore, the traditional typing methods
have given rise to a situation where a single anamorph can
have two different teleomorphs, suggesting that such
“species” actually contain more than one species.
A taxonomic method first proposed in 1999 defines
dermatophyte species by genetic techniques, specifically the
sequencing of highly variable internal transcribed spacer
(ITS) regions of the ribosomal DNA. Some authors have
adopted the ITS scheme. Others feel that its adoption is
premature and based on limited data. ITS taxonomy has been
criticized because it may place organisms into the same
species even when they seem to be ecologically distinct
based on their adaptation to different hosts; zoophilic,
anthropophilic or geophilic nature; or distinctive
characteristics such as opposite mating types or ability to
penetrate hair in vitro. In addition, the results of ITS typing
may not agree with the results of genetic analyses based on
other genes. Some sources also use traditional typing
schemes for practical reasons: genetic typing is not widely
used in diagnostic laboratories, and some species defined by
ITS sequencing can be difficult or impossible to identify by
conventional methods. This is especially true for T.
mentagrophytes.
Zoophilic or geophilic species that have new names,
under the ITS genetic system, include the following:
Horse-adapted isolates of M. canis, which do not
perforate hair in in vitro tests (unlike most M. canis)
and produce few conidia, were formerly called M.
equinum. Based on genetic relatedness, they are
now considered to be M canis.
The organism known as M. gypseum in the
traditional taxonomy contains both M. gypseum and
M. appendiculatum in the ITS system.
The species M. gallinae, a zoophilic organism
found in birds, includes the geophilic organism M.
vanbreuseghemii in the ITS system.
T. verrucosum varieties have been eliminated under
the current ITS genetic taxonomy, and this
organism is redefined to include only the species
adapted to cattle. The ITS system reassigns T.
verrucosum var. autotrophicum, which occurs in
sheep, to T. interdigitale.
The ITS system made major changes in the
taxonomy of T. mentagrophytes. In traditional
taxonomy, zoophilic and anthropophilic isolates of
T. mentagrophytes can be separated, in part, by their
different colony morphologies on primary isolation.
The species T. mentagrophytes var interdigitale is
anthropophilic in this system, and mainly contains
isolates associated with tinea pedis (athlete’s foot)
and infections of the nails. Under the ITS
taxonomy, however, most of the organisms that
previously belonged to T. mentagrophytes were
placed in this variety, and it was elevated to the
level of a species (T. interdigitale). Thus, T.
interdigitale in the ITS system includes both
anthropophilic organisms (the former T.
mentagrophytes var. goetzii, T. mentagrophytes var.
interdigitale, T. mentagrophytes var. nodulare and
T. krajdenii) and zoophilic organisms, including the
former T. mentagrophytes var. mentagrophytes, T.
mentagrophytes var. granulosum and T.
verrucosum var. autotrophicum. Under this system,
T. mentagrophytes still contains the former T.
mentagrophytes var. quinckeanum and two camel-
associated species, T. langeronii and T. sarkisovii.
In addition, the authors of the ITS scheme suggest
that all three of these species are associated with
camels, although T. mentagrophytes var
quinckeanum was previously linked mainly with
mice. The association of the latter organism with
camels has been disputed, and the entire
reorganization of T. mentagrophytes is
controversial.
Two other varieties of T. mentagrophytes received
new names in the ITS system. T. mentagrophytes
var. erinacei, which is adapted to hedgehogs, is now
considered to be the species T. erinacei. In addition,
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isolates of T. mentagrophytes found mainly in
guinea pigs (which were usually identified as T.
mentagrophytes var. granulosum) are now called
“the Trichophyton anamorph of A. benhamiae.”
This anamorph was not given a separate species
name. Although it is sometimes shortened to A.
benhamiae” in clinical literature, the A. benhamiae
complex also contains several other organisms
(e.g., T. erinacei, T. verrucosum and the
anthropophilic organism T. concentricum).
It should be noted that species names, as currently
defined under the ITS genetic taxonomy, may change in the
future. For instance, T. equinum, which is adapted to horses,
was reassigned to the anthropophilic species T. tonsurans at
one time; however, it was later acknowledged to be a
different species.
This factsheet generally uses the traditional taxonomy.
Geographic Distribution
Dermatophytes grow best in warm and humid
environments and are, therefore, more common in tropical
and subtropical regions. Their distribution varies with the
organism. M. canis, M. nanum, M. gypseum, T.
mentagrophytes, T. verrucosum and T. equinum, occur
worldwide, although their prevalence varies with the region.
T. simii was thought to be endemic only in Asia, specifically
the Indian subcontinent; however, infections acquired in
Europe and Africa suggest that its distribution might be more
widespread.. T. mentagrophytes var. erinacei (T. erinacei) is
associated with hedgehogs, and it is found where these
animals occur in the wild (Europe, New Zealand and Africa),
or in countries where they are kept as pets. M. persicolor has
been reported in Europe, and T. bullosum has been detected
in Tunisia, Sudan, Syria and France.
Like zoophilic species, anthropophilic dermatophytes
may be either cosmopolitan or more limited in their
distribution. The latter group may be imported into other
countries on infected individuals.
Transmission
People and animals become infected by dermatophytes
after contact with spores (conidia). Dermatophytes growing
in a vertebrate host normally form only arthrospores
(arthroconidia), asexual spores that develop within the
hyphae. In the environment (e.g., in laboratory culture), they
can also produce microconidia and macroconidia, asexual
spores that develop outside the hyphae. Initially, the
dermatophyte infects a growing hair or the stratum corneum
of the skin. These organisms do not usually invade resting
hairs, since the essential nutrients they need for growth are
absent or limited. Hyphae spread in the hairs and keratinized
skin, eventually developing infectious arthrospores.
Anthropophilic and zoophilic dermatophytes are mainly
transmitted between hosts by arthrospores in hairs or skin
scales. Other asexual or sexual spores formed by the
environmental stages may also be infectious. Fomites such
as brushes and clippers are important in transmission. Spores
may remain viable in suitable environments for up to 12-20
months, and some spores were also reported to persist for at
least a year in salt water. Certain types of spores (e.g.,
microconidia) might be dispersed by airborne means.
Disinfection
Dermatophyte spores are susceptible to benzalkonium
chloride, dilute chlorine bleach (1% sodium hypochlorite),
enilconazole (0.2%), formaldehyde and some strong
detergents. In one study, a 10% solution of
alkyldimetylbenzylammonium chloride prevented the growth
of M. canis from 97% of contaminated hairbrushes, and
Virkon-S® was effective on 87%. Another study found that a
preparation containing benzylammonium bromide and
ethoxyllauric alcohol was effective against the anthropophilic
fungi usually found on swimming room floors. Dermatophytes
are also reported to be susceptible to iodophors,
glutaraldehyde and phenolic compounds; however, some
agents may have limited efficacy in “real life” environmental
disinfection.
The mechanical removal of any material containing
keratin, such as shed skin and hairs, facilitates disinfection.
Vacuuming is considered to be the best method in many
cases. Dusting may also be appropriate. After mechanical
removal, washable surfaces should be cleaned thoroughly
with detergent and water.
Dermatophytes are susceptible to high heat. Moist heat
of 121°C, applied for at least 20 minutes, or dry heat of 165-
170°C for 2 hours, are reported to be effective.
Infections in Humans
Incubation Period
The incubation period in humans is usually 1 to 2 weeks.
Clinical Signs
Dermatophytes generally grow only in keratinized tissues
such as hair, nails and the outer layer of skin; the fungus
usually stops spreading where it contacts living cells or areas
of inflammation. Many dermatophytes can invade hairs as
well as the skin; however, some anthropophilic species such
as E. floccosum and T. rubrum are limited to the skin. Mucus
membranes are not affected.
The symptoms of dermatophytosis vary, depending on
the infecting organism, affected tissues (e.g., skin, hair or
nails) and area of the body. In unhaired (glabrous) skin, the
lesions are usually characterized by inflammation that is
most severe at the edges, with erythema, scaling and
occasionally blister formation. The central area may clear,
resulting in the formation of a classic “ringworm” lesion.
In haired areas, the hairs become brittle and areas of
alopecia may appear. Dermatophytes acquired from
animals or the soil generally produce more inflammatory
lesions than anthropophilic dermatophytes (but not all
individual cases are highly inflammatory). These infections
are also less likely to become chronic than those caused by
anthropophilic organisms
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In humans, dermatophytoses are referred to as “tinea”
infections, and are named according to the area of the body
involved. Infections can, however, spread from one area to
another. For example, tinea faciei (facial dermatophytosis) in
children may result from a tinea capitis (scalp) infection that
has spread to the face.
Tinea capitis
Tinea capitis, most often seen in children, is a
dermatophyte infection of the hair and scalp. The major
organisms involved in this condition vary with the
geographic area. M. canis, a zoophilic species, is often
isolated from tinea capitis cases in continental Europe;
however, the anthropophilic dermatophyte T. tonsurans is
currently responsible for most cases in the U.S. and the U.K.
Other anthropophilic organisms, whose importance varies
with the region, include T. violaceum, M. audouinii, T.
schoenleinii, T. megninii, T. soudanense and others. The
zoophilic organisms T. mentagrophytes, T. verrucosum, M.
persicolor and other species, as well the geophilic organisms
M. gypseum and (uncommonly) M. nanum, have been
isolated from some cases.
Tinea capitis is characterized by spreading, scaly,
irregular or well-demarcated areas of erythema and alopecia.
Some anthropophilic dermatophytes may cause dry alopecic
patches with minimal inflammation (sometimes with black
dots where the hairs break at the follicle). Zoophilic
dermatophytes are more likely to cause inflammatory, and in
some cases suppurative, lesions, including .boggy,
inflammatory masses called kerions. An anthropophilic
species, T. schoenleinii, causes “favus,” a chronic infection
characterized by yellow, cup shaped crusts (scutulae) around
the hairs. Untreated cases of tinea capitis can last for a month
to several years, depending on host factors and the species of
dermatophyte involved.
Tinea corporis
Tinea corporis, or ringworm, occurs on the trunk and
extremities (and in some definitions, the face). Infections
often spread to the neck and wrists of adults in contact with
infected children. Anthropophilic organisms that cause tinea
corporis include T. rubrum and E. floccosum, which infect
the skin but not the hair, as well as dermatophytes also found
in tinea capitis, such as M. audouinii, T. schoenleinii, T.
tonsurans and T. violaceum. Various zoophilic organisms
such as M. canis, T. verrucosum, T. equinum, T.
mentagrophytes and M. persicolor, as well as the geophilic
organisms M. gypseum and M. nanum can also cause this
form of tinea.
One or more lesions may be present in tinea corporis.
These lesions are usually pink to erythematous or scaly, and
annular with a slightly elevated, scaly and/or erythematous
edge, sharp margin, and central clearing. Follicular papules,
pustules or vesicles may be found on the borders, especially
when the lesion is caused by zoophilic or geophilic organisms.
The zoophilic organism T. quinckeanum can cause scutulae. In
contrast, some anthropophilic dermatophytes can cause
chronic lesions with little inflammation and very little scaling
at the edge. Lesions are variably pruritic. Treatment with
corticosteroids, or repeated shaving or occlusion of the
affected area, can result in skin lesions that do not resemble
the classic form. Untreated tinea corporis may resolve within
a few months, particularly if it is caused by a zoophilic or
geophilic organism, but infections caused by anthropophilic
organisms may be more persistent.
Tinea faciei and tinea barbae
Tinea faciei and tinea barbae are dermatophyte
infections occurring on the face. These infections are often
acquired from pets or livestock, but they can also be caused
by anthropophilic dermatophytes that originally affected
other parts of the body such as the scalp or torso.
Tinea barbae is an infection of the hairs and skin in the
beard and mustache area, and is usually seen in men. Some
causative organisms invade the hair and hair follicles, while
others (e.g., T. rubrum) are limited to the skin. The lesions of
tinea barbae may include scaling, follicular pustules and
erythema. The zoophilic organisms T. verrucosum
(associated with cattle) and T. mentagrophytes can cause a
very inflammatory form of this disease, with pustular
folliculitis or kerions. Some other species that may be
involved include M. canis, which is zoophilic, and the
anthropophilic organisms T. tonsurans, T. megninii and T.
violaceum. Some authors consider tinea barbae to be a form
of tinea faciei, rather than a separate condition.
Tinea faciei is seen on the nonbearded parts of the face.
It can be caused by a number of anthropophilic and zoophilic
organisms including T. rubrum, T. tonsurans, T.
schoenleinii, T. mentagrophytes, M. canis and T. erinacei.
The lesions are usually pruritic; itching and burning may
become worse after exposure to sunlight. While some lesions
may resemble those of tinea corporis, others have little or no
scaling or lack raised edges. In addition, the areas of
erythema may be indistinct. Due to these atypical
presentations, tinea faciei is often confused with other skin
diseases that affect the face.
Tinea cruris
Tinea cruris is an acute to chronic infection of the groin
and adjacent areas, usually caused by anthropophilic
dermatophytes. The most commonly involved organisms are
T. rubrum, T. mentagrophytes var. interdigitale and
E. floccosum, although the last species is now uncommon in
some areas. The symptoms include burning, pruritus, and
erythematous lesions with scales, raised, sharply demarcated
borders and central clearing. Pustules and vesicles are
sometimes found at the edges of the lesion. Macerated, moist
exudative forms or lesions with an eczematous appearance
can be present in acute cases, while dry lesions with little
scaling and an annular form are more characteristic of
chronic cases. Hyperpigmentation is common in the central
region as the lesion progresses. The same fungi can cause
tinea cruris and tinea pedis, and the two conditions may be
present concurrently.
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Tinea pedis and tinea manuum
Tinea pedis is usually caused by anthropophilic
dermatophytes such as T. rubrum, T. mentagrophytes var.
interdigitale and E. floccosum. Interdigital tinea pedis
(athlete’s foot) is an infection of the foot, characterized
either by dryness, fissures and scales or white, moist
macerated lesions in some or all of the spaces between the
toes. Another form of tinea pedis (the chronic,
erythematosquamous or moccasin” form) appears as
scaling of the soles and lateral surfaces of the feet, with
variable degrees of inflammation and dryness. A third form
of tinea pedis is characterized by erythema, vesicles,
pustules and bullae mainly on the soles of the feet. The nails
are also involved in many cases.
Tinea manuum is a dermatophyte infection that tends
to affect one hand, although involvement of both hands is
possible. In this form, the palms become diffusely dry,
scaly and erythematous. Inflammatory (vesicular or
pustular) lesions can be seen occasionally. Tinea manuum
is most often caused by anthropophilic dermatophytes,
particularly T. rubrum (cases are frequently an extension of
athlete’s foot) but occasional cases may be caused by
zoophilic organisms such as M. canis, T. mentagrophytes,
T. verrucosum and T. erinacei, or the geophilic organism
M. gypseum.
Tinea unguium
Tinea unguium (or onchomycosis) is a dermatophyte
infection of the nails. It is characterized by thickened,
opaque, discolored, broken and dystrophic nails. The nail
plate may be separated from the nail bed. Toenails are
affected more often than fingernails, and individual nails
are sometimes spared. There are several different forms of
tinea unguium, ranging from superficial, roughened white
patches to almost complete breakdown of the nail. Most
infections are caused by anthropophilic Trichophyton
species, particularly T. rubrum and less frequently T.
mentagrophytes var interdigitale. M. canis has been
involved occasionally in immunosuppressed patients.
Dermatophytes in immunosuppressed
individuals
In immunosuppressed individuals with impaired cell-
mediated immunity (e.g., HIV-infected patients with low T
cell counts, or organ transplant recipients), dermatophytes
can cause extensive lesions. In rare cases, they may also
penetrate more deeply into the skin than usual, resulting in
abscesses, exophytic nodules, and pseudomycetomas
(granulomatous or pyogranulomatous masses surrounding
fungal hyphae). Although pseudomycetomas can also occur
in healthy people, they are less common. Dissemination to
internal organs (e.g., lymph nodes, bones, spleen, brain,
liver) is possible, but very rare. Immunosuppressed patients
may also be extensively infected with species that rarely
affect healthy people, such as M. gallinae.
Communicability
Dermatophytes acquired from animals can be
transmitted between people, but this is uncommon and the
number of transfers is limited. In contrast, anthropophilic
dermatophytes are readily spread from person to person.
Anthropophilic dermatophytes can be transmitted to
animals, although this seems to be rare.
Diagnostic Tests
Diagnosis is based on the history, physical examination,
and microscopic examination of scrapings and hairs from the
lesions, sometimes in conjunction with fungal culture and
other techniques such as Wood’s lamp examination and
histology of the tissues.
Some dermatophytes fluoresce when they are stimulated
by the wavelengths of ultraviolet (UV) light in a Wood’s
lamp. Organisms that exhibit fluorescence include some
strains of the zoophilic dermatophytes M. canis and T.
quinckeanum, as well as a few anthropophilic species, such
as M. audouinii. T. tonsurans and T. violaceum, which are
the most common agents in some regions, are not revealed
by this technique. Certain topical preparations may mask the
fluorescence, and alcohol can either suppress it or cause non-
specific fluorescence.
Dermatophytes can often be detected by microscopic
examination of infected hairs and skin or nail scrapings.
Hyphae rounding up into arthroconidia are diagnostic, but
hyphae alone could be caused by other fungi, including
contaminants. In hairs, arthroconidia may be found outside
(ectothrix) or inside (endothrix) the hair shaft. Skin scrapings
should be taken from the edge of the lesion, and hairs should
be plucked (not cut) from this area. The best hairs to select
are those that fluoresce under a Wood's lamp, or are broken
or scaly. Nail scrapings are generally taken from the nail bed,
or from deeper portions of the nail after removing the outer
layers (except in cases where the infection is entirely
superficial). Samples are usually cleared with potassium
hydroxide (KOH) or other agents to help visualize the
organism. Various stains such as chlorazol black E, Parker
blue-black ink, Swartz-Lamkin stain or Congo red stain may
be added. Fluorescence microscopy, using calcofluor white
or other stains, can also be used to visualize dermatophyte
structures.
Fungal cultures, which identify the species of
dermatophyte, can be useful in understanding the source of
the infection and targeting preventive measures appropriately.
Culture may also be necessary if the diagnosis is uncertain, or
the infection is resistant to standard treatment. However,
recommendations vary in the literature, and uncomplicated
cases are not always cultured in practice. Samples for culture
include hair, skin and nail samples, as for microscopic
examination. In some situations (e.g., infections in sensitive
sites, or the identification of asymptomatic carriers), other
techniques such as brushing the hair, using adhesive tape to
collect samples, or rubbing the area with a sterile toothbrush
or moistened, sterile cotton swab may also be effective.
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Colonies appear in 5 days to 4 weeks, depending on the
organism. Colony morphology can differ with the medium.
Descriptions are usually based on Sabouraud agar, but
dermatophyte medium or other fungal culture media can also
be used for isolation. Dermatophyte species can be identified
by the colony morphology; the appearance of microconidia,
macroconidia and other microscopic structures; biochemical
characteristics such as urease production; and nutritional
requirements. Specialized tests such as the ability to penetrate
hairs in vitro, or mating tests (which are usually available only
at reference laboratories) may be used occasionally.
Differential media (e.g., bromocresol purple-milk solids
glucose) can be helpful during differentiation. Some fungal
cultures from infected people are negative.
Histology (biopsy) is occasionally helpful, especially in
deep mycoses and some infections of the nails. The
organisms are visualized best with periodic acidSchiff
(PAS) staining, although they may also be found in
hematoxylin-eosin stained preparations.
PCR tests have been published for a number of
organisms, and molecular methods of diagnosis might
become more common in the future.
Treatment
Dermatophyte infections are treated with a variety of
topical and oral antifungal drugs.
In immunocompetent patients, topical agents are usually
effective in cases that are limited to glabrous skin (e.g., tinea
corporis, tinea cruris, and tinea pedis). Systemic (oral)
antifungal drugs may be necessary in severe cases, or if the
infection does not respond to treatment or reappears.
Topical agents are ineffective against organisms that
infect the hairs. These infections are usually treated with
systemic antifungals, although topical lotions or shampoos
are sometimes used concurrently to decrease shedding of
fungi and spores, or to help treat kerions. Topical agents may
also be used to treat asymptomatic carriers or prevent
reinfection. Tinea capitis is reported to be more difficult to
treat when it is caused by M. canis than Trichophyton spp.
and may not respond as well to some drugs.
Dermatophyte infections of the nails (tinea unguium) are
usually treated with oral antifungal drugs. Concurrent
therapies may include debridement of the nail or nail avulsion.
Treatment should consider sources of reinfection, such
as pets, family members or other close contacts. Some
authors suggest treating all family members when the case is
caused by certain anthropophilic organisms.
Prevention
Controlling dermatophytes in animals can prevent some
cases of zoonotic dermatophytosis in humans. Infected
animals should be treated, and the premises and fomites
cleaned and disinfected as much as possible. (Some
environments can be difficult to decontaminate.) Contact with
infected animals should be limited, and gloves and protective
clothing should be used if these animals are handled.
Better surveillance, improved living conditions and
improved treatments can decrease the overall prevalence of
anthropophilic dermatophytes, while hygiene, and
prevention of contact are helpful in individual cases.
Measures such as moisture control (e.g., in tinea pedis) are
important in reducing susceptibility to some forms of tinea.
Morbidity and Mortality
Dermatophyte infections are common in people,
although the prevalence varies with the climate and various
risk factors including animal contact. Up to 60% of children
may be affected by tinea capitis in some regions, and more
than 50% of the population in some parts of Europe is
reported to have tinea pedis. With the exception of tinea
cruris (which is typically seen in adults), dermatophytosis is
more common in children.
Exposure to dermatophyte spores does not always lead
to infection. Skin injuries (e.g., burns, maceration or
chafing), as well as high temperatures and humidity, increase
susceptibility. For example, tinea cruris is more common in
hot climates and in people who wear tight clothing.
Most dermatophyte infections are not serious in healthy
people, although some conditions are easier to treat than
others. Infections in glabrous skin usually resolve within 2-4
weeks with treatment. In contrast, dermatophytosis of the nails
may be difficult to cure (although the prognosis is better with
newer drugs), and relapses can occur. In addition, damaged
nails do not always return to a normal appearance even if the
fungal infection is eliminated. Infections with opportunistic
bacteria can cause cellulitis in skin damaged by interdigital
fungal infections, and are a particular concern in diabetics.
Dermatophytosis has the potential to be more serious in
immunosuppressed individuals, who may have atypical and
locally aggressive dermatophyte infections, including
extensive skin disease and subcutaneous abscesses.
Disseminated disease is also possible, though very rare.
Infections in Animals
Species Affected
All domesticated mammals are susceptible to
dermatophytes. Wildlife can also be affected. The most
common agents vary with the host and the geographic region,
and may also be affected by management practices (e.g.,
whether animals can contact other species). Overall, the most
common dermatophytes in domesticated mammals are M.
canis, M. gypseum, T. mentagrophytes, T. verrucosum, T.
equinum and (in pigs) M. nanum. Birds can also be affected by
some organisms, such as M. gallinae and T. mentagrophytes.
Reptiles are not usually affected by the dermatophytes
of mammals or birds; however, rare clinical cases associated
with Trichophyton spp. have been reported in lizards, snakes
(green anacondas, Eunectes murinus) and an olive ridley sea
turtle (Lepidochelys olivacea). One case report in iguanas
identified the species as T. interdigitale, possibly of
anthropophilic origin.
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Zoophilic dermatophytes
Microsporum canis is the most common species of
dermatophyte in cats and dogs, with cats considered
to be the most important reservoir hosts. This
organism is also found regularly in horses and
rabbits, and it has been reported in other animals
including cattle, sheep, goats, camelids and swine.
Isolates that appear to be adapted to horses were
previously called Microsporum equinum, but were
moved to M. canis based on genetic analyses.
Microsporum gallinae occurs in birds, including
poultry. This organism seems to be uncommon in
wild birds. Infections are reported occasionally in
mammals including livestock, especially in some
parts of the world.
Microsporum persicolor primarily affects wild
rodents (bank voles and mice). It is found
occasionally in other species, especially rabbits and
pigs, and dogs that burrow and hunt rodents. This
organism infects the skin, but does not invade hairs.
Trichophyton bullosum has been found in horses. It
is related to T. verrucosum.
Trichophyton equinum, adapted to horses, is an
important cause of dermatophytosis in this species.
Infections have also been reported in cats, dogs,
goats, sheep and other species.
Trichophyton langeronii seems to be adapted to
camels.
Trichophyton mentagrophytes has been reported in
many species of animals, especially rodents and
rabbits. It also affects horses, ruminants, swine,
cats, dogs, birds and other hosts.
T. mentagrophytes var. erinacei (or T. erinacei)
occurs in the European hedgehog (Erinaceus
europeus) and the African hedgehog (Atelerix
albiventris). It is seen in pet hedgehogs as well as
animals in the wild. This organism sometimes
occurs in hunting dogs.
T. mentagrophytes var. granulosum affects rodents.
One group of organisms, (identified as “the
Trichophyton anamorph of A. benhamiae” in the
ITS taxonomy) is often associated with guinea pigs,
and appears to the most common dermatophyte in
this species.
T. mentagrophytes var. quinckeanum has
traditionally been associated with mice. However,
it is considered to be a camel-associated isolate in
the ITS genetic taxonomy.
Trichophyton sarkisovii seems to be adapted to
camels.
Trichophyton simii affects nonhuman primates, but
some authors believe the primary host is a ground-
dwelling animal. It has also been reported from
other mammals and birds.
Trichophyton verrucosum, which is adapted to
cattle, is the most important dermatophyte in this
species. T. verrucosum readily infects other hosts,
especially sheep, goats, South American camelids
and camels, but it can also be found occasionally in
other species such as horses, donkeys, pigs, dogs
and rabbits.
T. verrucosum var. autotrophicum affects sheep.
Geophilic species
M. gypseum is detected occasionally in a wide
variety of animals, including cats and dogs,
ruminants, camelids, horses, pigs, rodents, rabbits,
birds and others. It is the most frequently isolated
geophilic dermatophyte in animals.
M. nanum is the most important agent in swine. This
dermatophyte is thought to be uncommon in most
other species, although it has been found
occasionally in rabbits and cattle.
Anthropophilic species
Anthropophilic dermatophytes are reported infrequently
in animals (although it is possible that some of these reverse
zoonoses are missed). Some species that have been
documented in case reports include M. audouinii, T.
schoenleinii, T. rubrum, T. tonsurans, T. violaceum and E.
floccosum. Livestock (e.g., a goat) as well as pets have been
infected. Potential predisposing factors, such as tumors or
treatment with immunosuppressive drugs, were reported in
some cases.
Incubation Period
Fluorescence produced by some dermatophytes, such as
M. canis, can appear on the fur within 7 days of exposure,
and clinical signs can develop within 2 to 4 weeks.
Clinical Signs
Dermatophytes usually grow only in keratinized tissues
such as hair, nails and the outer layer of skin; the fungus stops
spreading where it contacts living cells or areas of
inflammation. Mucus membranes are not affected.
Dermatophyte lesions in animals are characterized by
areas with varying degrees of alopecia, scaling, crusts and
erythema, and may or may not be pruritic. Hairs in the
affected area are usually brittle and break near the skin
surface, often giving the lesion a “shaved” appearance;
truncated hair shafts may be seen through the scales and
crusts. Occasionally, dermatophytes may die at the center of
a lesion and that area resolves, leaving a circular lesion with
central crusts or hair regrowth. Some degree of folliculitis
occurs in most cases; papules or pustules involving the hair
follicle or conical dilation of the hair follicle ostium are
suggestive of dermatophytosis in small animals.
Asymptomatic infections are also common, particularly in
adult animals.
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Cats
Many cats infected with dermatophytes have few or no
lesions. Long-haired adults, in particular, can be subclinical
carriers or have only minimal signs, such as patchy areas of
short stubble, alopecia, scales or erythematous plaques,
visible only on close inspection. More apparent cases tend
to be seen in kittens, with the early lesions often found on
the face, ears and paws. In addition to focal alopecia and
scales, affected areas may develop a thin, grayish white
crust or a thick, moist scab. They may or may not be
pruritic. The cat’s grooming behavior may eventually
spread the infection to the entire body. Other presentations
that have been reported in cats include miliary dermatitis
and recurrent chin acne. Severe cases of dermatophytosis,
with large, erythematous, alopecic, exudative lesions, may
be seen in debilitated cats, or in animals that have been
treated with corticosteroids. Onchomycosis can occur
concurrently in cats with dermatophytosis; the nails may be
opaque, with whitish mottling, and shredding of the nail
surface.
In some cats, dermatophytosis may appear as one or
more firm, subcutaneous nodules known as
pseudomycetomas, Pseudomycetomas tend to occur in long-
haired cats, especially Persians, and are most often found on
the back and the neck. They sometimes ulcerate or form
draining sinus tracts. Some cats, but not others, have
concurrent cutaneous signs such as alopecia and scaling.
True mycetomas have also been reported, though rarely.
Uncomplicated dermatophyte lesions are usually self-
limiting within a few weeks to a few months in short-haired
cats; however, the organisms may persist, either
symptomatically or asymptomatically, in long-haired cats.
Dogs
Dermatophytosis is seen most often in puppies. The
lesions frequently develop on the face and limbs, although
they may occur on any part of the body. M. canis tends to
appear as small circular areas of alopecia. The hairs are
typically broken at the base, giving the appearance of having
been shaved. The center of the lesion usually contains pale
skin scales in the early stage, giving it a powdery appearance,
and the edges are generally erythematous. Vesicles and
pustules may also be seen. In later stages, the area is often
covered by a crust and the edges swollen. Individual lesions
may coalesce to form large, irregular patches. Lesions caused
by T. mentagrophytes and T erinacei tend to be more
thickened and inflammatory than those caused by M. canis,
while M persicolor typically causes localized or generalized
scaling with little erythema and minimal alopecia. Other forms
of dermatophytosis can include kerions (localized severe
inflammation with swollen, boggy skin oozing pus) and
pseudomycetomas. Onchomycosis may occur concurrently
with dermatophytosis.
Although dermatophytosis is often self-limited in dogs,
some animals can develop severe, chronic cases with
widespread lesions, and severe inflammation and alopecia.
Generalized cases in adult dogs usually occur in
immunosuppressed animals, especially those that have
hyperadrenocortictropism or have been treated with
corticosteroids.
Horses
In horses, most dermatophyte lesions are found in areas
of contact with saddles or other tack. They usually begin as
small patches of raised hairs, and progress to hair loss, with
variable amounts of scaling, erythema, crusting and
exudation. M. canis lesions are reported to be milder, in most
cases, than T equinum. Kerions may occur in some animals,
especially on the face. Miliary dermatitis may also be seen,
with small crusted lesions especially on the flanks. Early
dermatophyte lesions can sometimes resemble papular
urticaria, but more characteristic signs develop within a few
days. Lesions may coalesce, especially where the skin is
abraded from tack.
Cattle
In cattle, dermatophytosis varies from small focal
lesions to extensive generalized skin involvement. The initial
lesions may be discrete, scaly and alopecic with grayish-
white crusts, and tend to appear on the face and neck in
calves. Cows and heifers may have lesions more often on the
chest and limbs, and bulls on the dewlap and intermaxillary
skin. Some areas may become suppurative and thickly
crusted. Lesions resembling light brown scabs may also be
seen; when these scabs fall off, they leave an area of alopecia.
The clinical signs usually resolve spontaneously in 2 to 4
months.
Sheep and goats
Dermatophytosis tends to be seen in show lambs, but
appears to be uncommon in production flocks. The most
noticeable signs are usually circular, alopecic areas with
thick scabs on the head, face and non-wooled areas of the
legs; however, widespread lesions may be found under the
wool when lambs are sheared for showing. In healthy lambs,
the disease is usually self-limiting.
Swine
Pigs may develop a wrinkled lesion covered by a thin,
brown, easily removed scab, or a spreading ring of
inflammation. Dermatophyte infections are often
asymptomatic in adult swine.
Rodents
Most rodents infected with T. mentagrophytes are
asymptomatic or have few clinical signs. There may be areas
of partial or complete alopecia, erythema, scales, and crusts
in symptomatic animals. In guinea pigs, the lesions tend to
appear first on the face, then spread to the back and limbs. In
mice, the lesions are often found on the tail.
Rabbits
Focal alopecia, with erythema, crusts, scales and scabs,
is initially seen mainly around the eyes, nose, ears and dorsal
neck. The lesions may later spread to other areas of the body.
The disease is usually self-limiting.
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Hedgehogs
Asymptomatic infections are common in hedgehogs. In
symptomatic animals, scales may be found on the head, base
of the nails and under the pads, but lesions are difficult to see
between the spines.
Birds
In cage birds, there may be alopecia and scales,
particularly on the face, head, neck and chest, as well as auto-
mutilation and feather plucking. The head and neck,
especially the comb, are often affected in fowl. The lesions
may include white crusts or plaques and hyperkeratosis.
Although feathers may be lost in birds, they are not infected.
Reptiles
Reptiles are not usually affected by the dermatophytes
of mammals or birds; however, there are rare case reports of
dermal lesions in lizards and green anacondas. Clinical signs
reported during a Trichophyton outbreak in iguanas included
scaling, crusting, thickening of the skin and ulcerative
dermatitis. Trichophyton spp. infection was associated with
papular and pustular cutaneous lesions in a Tenerife lizard.
This animal died of an undetermined illness, soon afterward.
Trichophyton spp. was also detected by
immunohistochemistry from systemic lesions in a moribund
sea turtle.
Communicability
Most animal dermatophytes are readily transmitted to
other susceptible hosts, including humans, by contact and
contamination of the environment. M. nanum of pigs and T.
gallinae of birds are generally reported to be uncommon in
healthy people; however, this may not be the case in all
locations. One study found that T. gallinae was the third most
frequent dermatophyte of children in Nigeria.
Post Mortem Lesions Click to view images
Gross post-mortem lesions are usually identical to those
in live animals; with the exception of pseudomycetomas and
mycetomas, dermatophytes are restricted to the hair, nails
and superficial skin.
Diagnostic Tests
Dermatophytosis is usually diagnosed by a combination
of direct microscopic examination, culture and Wood’s lamp
examination. Biopsy (histopathology) tends to be used
mainly when the presentation is unusual.
A Wood’s lamp examination for fluorescence can be
helpful in detecting some species of dermatophytes, such as
M. canis and T. quinckeanum. Not all strains of these
organisms exhibit fluorescence. Certain topical preparations
may mask the fluorescence, and alcohol can either suppress
it or cause non-specific fluorescence.
Microscopic examination of skin scrapings or plucked
hairs may reveal hyphae or arthroconidia. Hyphae rounding
up into arthroconidia are diagnostic; however, hyphae alone
could be caused by other fungi, including contaminants.
Samples should be selected from the margins of active lesions,
or from the entire lesion if there is no inflammatory margin.
The best hairs to select are those that fluoresce under a
Wood's lamp, or are broken or scaly. Samples are usually
cleared with potassium hydroxide (KOH) to help visualize
the organism, although other clearing agents may be used. A
longer clearing time can be helpful when the hair is thicker
and more heavily pigmented, or if the sample is taken from
a thick, crusted lesion. Various stains such as chlorazol black
E, Parker blue-black ink, Swartz-Lamkin stain, Congo red
stain or Giemsa can aid the visualization of fungal structures.
In practices where fluorescence microscopy is available,
calcofluor white staining can be used.
Skin scrapings or plucked hair samples for culture should
be taken from active lesions, as for microscopic examination.
Nail beds and claws are cultured in cases of onchomycosis.
Swabbing dermatophyte lesions first with alcohol may
decrease contaminants, especially in livestock. Additional
collection methods, which are especially helpful in
asymptomatic animals suspected of being carriers, including
brushing the fur with a disinfected toothbrush or other small
brush, or rubbing it with a sterile piece of carpet.
Dermatophytes can be cultured on various fungal media,
including Sabouraud agar (with cycloheximide and
antibiotics) and dermatophyte test medium (DTM). Cultures
are usually incubated at room temperature (2028ºC), but
higher temperatures can be used when certain organisms
(e.g., T. verrucosum) are suspected. Colonies often become
visible within 1-2 weeks but, some species grow more slowly
and may require longer to appear. Colony morphology can
differ with the medium; descriptions are usually based on
Sabouraud agar. DTM contains a pH indicator (phenol red)
that will turn the medium red when a dermatophyte is growing.
However, the mycelial growth must also be examined
microscopically, as this color change alone is not diagnostic
and could be produced by other fungal or bacterial organisms.
In addition, the color change may be delayed with certain
dermatophytes such as M. persicolor. In asymptomatic
animals, caution must be used to distinguish infection from
contamination of the coat with organisms from the
environment.
Dermatophyte species can be identified by the colony
morphology; the appearance of microconidia, macroconidia
and other microscopic structures; biochemical characteristics
such as urease production; and nutritional requirements.
Microconidia and macroconidia can be used to distinguish the
genera Microsporum, Trichophyton and Epidermophyton.
Members of Microsporum spp. produce microconidia and
rough-walled, multiseptate macroconidia. The thickness of
the wall, shape and number of macroconidia vary with the
species. Trichophyton spp. produce microconidia and
smooth, thin-walled, cigar shaped macroconidia.
Macroconidia are rarely seen with some species. E.
floccosum, which is anthropophilic and has very rarely been
reported in animals, produces large, thin-walled,
multicellular, club-shaped, clustered macroconidia. This
organism does not produce microconidia. Specialized tests,
such as the ability to penetrate hairs in vitro, or mating tests
Dermatophytosis
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performed at reference laboratories, may occasionally be
used in the differentiation process. Differential media (e.g.,
bromocresol purple - milk solids glucose) can also be
helpful.
Histology may be used in some cases, especially in
animals with pseudomycetomas. The organisms are
visualized best with periodic acidSchiff (PAS) staining,
although they may also be found in hematoxylin-eosin
stained preparations.
PCR tests have been published for a number of
organisms, including zoophilic organisms, and molecular
methods of diagnosis might become more common in the
future.
Treatment
Healthy animals often have self-limiting infections that
resolve within a few months, but treatment can speed
recovery, prevent the lesions from spreading, and decrease
the risk of transmission to people or other animals. Some
individual animals, particularly those that are debilitated or
unusually susceptible, may not clear the infection without
treatment.
Drugs available to treat dermatophytosis in animals
include topical antifungal creams or shampoos, and systemic
antifungals. The same treatment principles apply in animals
as people; however, practical considerations limit the use of
systemic antifungals in some species. Topical drugs are
unable to eliminate dermatophytes from within hairs and hair
follicles, but they may be effective against organisms in
superficial sites (e.g., in the skin), and they can decrease
contamination and transmission to others. The optimal
treatment in small animals is combined topical and systemic
treatment. Systemic antifungals are rarely used in large
animals, due to the cost of these drugs and the typically self-
limited nature of the disease. The side effects of systemic
drugs should also be taken into consideration when choosing
a treatment plan. Clipping the hair before treatment is
controversial. It may aid the penetration of topical drugs, as
well as remove infected hairs. However, it may also result in
trauma to the skin and help disseminate the infection. If the
animal is clipped, this should be done with care.. Some
animals such as cattle develop thick crusts, which should be
removed by gentle brushing.
Onchomycosis can be very difficult to cure; long term
treatment or surgical declawing may be necessary.
Pseudomycetomas and mycetomas are also reported to be
difficult to treat, often recur after surgery, and may not respond
to some drugs. Nevertheless, some cases have been treated
successfully with drugs and/or surgery.
Animals should be isolated until the infection resolves.
Confining the animal to an environment that is easily cleaned
can facilitate environmental control. Dermatophytes can be
difficult to eradicate from environments such as kennels,
catteries and animal shelters.
Prevention
To prevent the introduction of dermatophytes into herds
or kennels, newly acquired animals should be isolated and
cultured. Wild rodent control can decrease exposure to T.
mentagrophytes. Some organisms can be acquired by contact
with infected soil.
To prevent infected animals from transmitting
dermatophytes to others, they should be isolated until the
infection has resolved. The premises should be cleaned and
disinfected. Some environments (e.g., barns) may be difficult
or impossible to decontaminate completely. Animals that
have been in contact with the patient should be checked for
asymptomatic infections. Some veterinarians use topical
antifungals prophylactically for in-contact animals.
Dermatophytes can be difficult to eradicate from
environments such as kennels, catteries and animal shelters.
Successful treatment of these premises must be based on
good environmental control, as well as treatment of
symptomatically and asymptomatically infected animals.
Vaccines are available in some countries for certain
organisms, such as T. verrucosum and T. mentagrophytes in
livestock, farmed foxes, chinchillas and rabbits; T. equinum
in horses; and M canis in cats and dogs. A feline vaccine
licensed for M. canis in the U.S. was found to be ineffective
under field conditions, and was withdrawn by the
manufacturer in 2003. Studies of other vaccines have
demonstrated varying efficacy.
In some countries, vaccines have been used in
dermatophyte eradication campaigns for cattle. In Norway,
there is a program to eradicate T. verrucosum from cattle
herds by vaccination, disinfection of contaminated stables,
isolation of infected animals and good hygiene. In one region
of Norway, where 95% of herds participated, the prevalence
of cattle ringworm decreased from 70% to 0% over a period
of 8 years. In the former Soviet Union, a vaccination
campaign reduced the prevalence of T. verrucosum in cattle
to less than 1% by 1984.
Morbidity and Mortality
Whether an animal becomes infected after contact with
a dermatophyte may depend on the animal’s age, the
condition of its exposed skin, general health and grooming
behavior. Young animals, including puppies, kittens, calves,
lambs and young camelids, are more likely to have
symptomatic infections than adults. Clinical
dermatophytosis is also thought to be more common in
immunosuppressed animals. Most infections in healthy
animals heal spontaneously within one to a few months. Hair
loss is not permanent unless the follicle has been destroyed
by inflammation. Infections can be more persistent or
widespread in young or sick animals. Breeds reported to
more susceptible to dermatophytes include some long haired
cats, and possibly Yorkshire terriers. Long-haired cats,
especially Persians, are also more likely to develop
pseudomycetomas and mycetomas.
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Dermatophytes can be isolated from animals with or
without clinical signs. Highly variable infection rates,
between 6% and 100%, have been reported in surveys of cats,
which are thought to carry these organisms more often than
dogs. Infections are especially prevalent in strays and in
catteries. The estimated prevalence among pet cats and dogs
in individual households is still unclear. While some surveys
suggest that many cats are infected with these organisms, one
University of Wisconsin study did not detect dermatophytes in
any of 182 asymptomatic pet cats that lived alone with their
owners.
Among livestock, dermatophytes are particularly
common in cold climates where animals are stabled for long
periods of time. This disease usually becomes endemic in
cattle herds, where it most often affects animals under a year
of age. The lesions tend to develop in cattle when they are
stabled indoors in winter, and to resolve when they are turned
out in the spring.. Clinical cases do not seem to be common
in sheep and goats, with the exception of show lambs;
however, M. canis caused some outbreaks that affected 20-
90% of sheep herds in Australia. It is possible that cases are
underdiagnosed in small ruminants. Infected animals are
reported to be common on rabbit farms in some countries.
Clinical cases seem to be infrequent in birds.
Internet Resources
Centers for Disease Control and Prevention (CDC)
Canadian National Centre for Mycology. World of
Dermatophytes: A Pictorial
National Institutes of Health
The Merck Manual
The Merck Veterinary Manual
Acknowledgements
This factsheet was written by Anna Rovid Spickler, DVM,
PhD, Veterinary Specialist from the Center for Food
Security and Public Health. The U.S. Department of
Agriculture Animal and Plant Health Inspection Service
(USDA APHIS) provided funding for this factsheet through
a series of cooperative agreements related to the
development of resources for initial accreditation training.
The following format can be used to cite this factsheet.
Spickler, Anna Rovid. 2013. Dermatophytosis. Retrieved
from http://www.cfsph.iastate.edu/DiseaseInfo/
factsheets.php.
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