You are in: eMedicine Specialties > Dermatology > FUNGAL INFECTIONS Tinea PedisArticle Last Updated: Sep 5, 2007AUTHOR AND EDITOR INFORMATIONAuthor: Courtney M Robbins, MD, Resident Physician, Department of Dermatology, University of Alabama at Birmingham School of Medicine Courtney M Robbins is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Medical Association, and Women's Dermatologic Society Coauthor(s): Boni E Elewski, MD, Professor, Department of Dermatology, University of Alabama at Birmingham Editors: Gregory J Raugi, MD, PhD, Professor, Department of Internal Medicine, Division of Dermatology, University of Washington at Seattle; Chief, Dermatology Section, Primary and Specialty Care Service, Veterans Administration Medical Center of Seattle; Michael J Wells, MD, Associate Professor, Department of Dermatology, Texas Tech University Health Sciences Center; Lester F Libow, MD, Dermatopathologist, South Texas Dermatopathology Laboratory; Catherine Quirk, MD, Clinical Assistant Professor, Department of Dermatology, Brown University; William D James, MD, Paul R Gross Professor of Dermatology, University of Pennsylvania School of Medicine; Vice-Chair, Program Director, Department of Dermatology, University of Pennsylvania Health System Author and Editor Disclosure Synonyms and related keywords: athlete's foot, ringworm of the feet, dermatophytosis, dermatophytid, Trichophyton rubrum, T rubrum, Trichophyton mentagrophytes, T mentagrophytes, Epidermophyton floccosum, E floccosum, Scytalidium hyalinum, S hyalinum, Scytalidium dimidiatum, S dimidiatum INTRODUCTIONBackgroundTinea pedis has afflicted humanity for centuries, so it is perhaps surprising that the condition was not described until Pellizzari did so in 1888. The first report of tinea pedis was in 1908 by Whitfield, who, with Sabouraud, believed that tinea pedis was a very rare infection caused by the same organisms that produce tinea capitis. Tinea pedis is the term used for a dermatophyte infection of the soles of the feet and the interdigital spaces. It is most commonly caused by Trichophyton rubrum, a dermatophyte initially endemic only to a small region of Southeast Asia and in parts of Africa and Australia. Interestingly, tinea pedis was not noted in these areas then, possibly because these populations did not wear occlusive footwear. The colonization of the T rubrum–endemic regions by European nations helped to spread the fungus throughout Europe. Wars with accompanying mass movements of troops and refugees, the general increase in available means of travel, and the rise in the use of occlusive footwear have all combined to make T rubrum the world's most prevalent dermatophyte. The first reported case of tinea pedis in the United States was noted in Birmingham, Alabama, in the 1920s. World War I troops returning from battle may have transported T rubrum to the United States. PathophysiologyT rubrum, Trichophyton mentagrophytes, and Epidermophyton floccosum most commonly cause tinea pedis, with T rubrum being the most common cause worldwide. Trichophyton tonsurans has also been implicated in children. Nondermatophyte causes include Scytalidium dimidiatum, Scytalidium hyalinum, and, rarely, Candida species. Using enzymes called keratinases, dermatophyte fungi invade the superficial keratin of the skin, and the infection remains limited to this layer. Dermatophyte cell walls also contain mannans, which can inhibit the body's immune response. T rubrum in particular contains mannans that may reduce keratinocyte proliferation, resulting in a decreased rate of sloughing and a chronic state of infection. Temperature and serum factors, such as beta globulins and ferritin, appear to have a growth-inhibitory effect on dermatophytes; however, this pathophysiology is not completely understood. Sebum also is inhibitory, thus partly explaining the propensity for dermatophyte infection of the feet, which have no sebaceous glands. Host factors such as breaks in the skin and maceration of the skin may aid in dermatophyte invasion. The cutaneous presentation of tinea pedis is also dependent on the host's immune system and the infecting dermatophyte. FrequencyInternationalTinea pedis is thought to be the world's most common dermatophytosis. Reportedly, 70% of the population will be infected with tinea pedis at some time. Mortality/MorbidityTinea pedis is not associated with significant mortality or morbidity. RaceTinea pedis has no predilection for any racial or ethnic group. SexThe disease more commonly affects males compared with females. AgeThe prevalence of tinea pedis increases with age. Most cases occur after puberty. Childhood tinea pedis is rare. CLINICALHistoryCommonly, patients describe pruritic, scaly soles and, often, painful fissures between the toes. Less often, patients describe vesicular or ulcerative lesions. Some patients, especially elderly persons, may simply attribute their scaling feet to dry skin. PhysicalPatients with tinea pedis have the following 4 possible clinical presentations:
Patients may have other associated dermatophyte infections, such as onychomycosis, tinea cruris, and tinea manuum. Tinea manuum is often unilateral and associated with moccasin-type tinea pedis (two feet–one hand syndrome). Causes
DIFFERENTIALSCandidiasis, Cutaneous Contact Dermatitis, Allergic Dyshidrotic Eczema Erythema Multiforme Erythrasma Friction Blisters Pityriasis Rubra Pilaris Psoriasis, Plaque Psoriasis, Pustular Syphilis
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| Drug Name | Clotrimazole 1% (Mycelex, Lotrimin) |
|---|---|
| Description | Broad-spectrum antifungal agent that inhibits yeast growth by altering cell-membrane permeability, causing death of fungal cells. Reevaluate diagnosis if no clinical improvement after 4 wk. |
| Adult Dose | Gently massage into affected area and surrounding skin areas bid for 2-6 wk |
| Pediatric Dose | Children: Not established Adolescents: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | For external use only; avoid contact with eyes; discontinue if irritation or sensitivity develops |
| Drug Name | Econazole 1% cream (Spectazole Topical) |
|---|---|
| Description | Effective in cutaneous infections. May interfere with RNA and protein synthesis and metabolism. Disrupts cell membrane permeability, causing death of fungal cells. |
| Adult Dose | Apply sparingly over affected areas qd/bid for 4 wk |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Discontinue if sensitivity or irritation develops; for external use only; avoid contact with eyes |
| Drug Name | Ketoconazole 1% cream (Nizoral) |
|---|---|
| Description | Imidazole broad-spectrum antifungal agent; inhibits synthesis of ergosterol, causing cellular components to leak, resulting in death of fungal cells. |
| Adult Dose | Rub gently into affected area bid/qid for 2-4 wk |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; fungal meningitis |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Discontinue if sensitivity or irritation develops; for external use only; avoid contact with eyes |
| Drug Name | Miconazole (Monistat) |
|---|---|
| Description | Damages fungal cell wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased, causing nutrients to leak out, resulting in fungal cell death. The 2% lotion is preferred in intertriginous areas. If the 2% cream is used, apply sparingly to avoid maceration effects. |
| Adult Dose | Cream and lotion: Cover affected areas bid for 2-6 wk Powder: Spray or sprinkle liberally over affected area bid for 2-4 wk |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Discontinue if sensitivity or chemical irritation occurs; for external use only; avoid contact with eyes |
| Drug Name | Oxiconazole 1% cream (Oxistat) |
|---|---|
| Description | Damages fungal cell wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased, causing nutrients to leak out, resulting in death of fungal cells. |
| Adult Dose | Apply to affected area bid for 4 wk |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Discontinue if sensitivity or chemical irritation occurs; for external use only; avoid contact with eyes |
| Drug Name | Sertaconazole nitrate cream (Ertaczo) |
|---|---|
| Description | Topical imidazole antifungal active against T rubrum, T mentagrophytes, and E floccosum. Indicated for tinea pedis. |
| Adult Dose | Apply topically bid to clean, dry skin between toes and immediate surrounding healthy skin for 4 wk |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | For topical use only; may cause dermatitis, dry skin, burning sensation, pruritus, hyperpigmentation, desquamation, or skin tenderness |
Broad-spectrum agents with antidermatophytic, antibacterial, and anticandidal activity and are therefore useful in all forms of tinea pedis but especially effective in interdigital tinea pedis.
| Drug Name | Ciclopirox 1% cream (Loprox) |
|---|---|
| Description | Interferes with synthesis of DNA, RNA, and protein by inhibiting transport of essential elements in fungal cells. |
| Adult Dose | Massage into affected area bid; reevaluate diagnosis if no improvement after 4 wk |
| Pediatric Dose | <10 years: Not established >10 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Avoid contact with eyes and other internal routes; discontinue if irritation or sensitivity develops |
Effective in treating all forms of tinea pedis. In vitro, these agents have demonstrated potent activity against dermatophyte fungi, so they are useful in treating patients with refractory tinea pedis (eg, chronic hyperkeratotic). Terbinafine 1% (Lamisil) has been shown to be effective in some patients with interdigital tinea pedis with only 1 wk of treatment. Patients with chronic hyperkeratotic tinea pedis generally require 4 wk of treatment.
| Drug Name | Naftifine 1% cream and gel (Naftin) |
|---|---|
| Description | Broad-spectrum antifungal agent and synthetic allylamine derivative; may decrease synthesis, which, in turn, inhibits growth of fungal cells. |
| Adult Dose | Cream: Apply to affected area qd for 4 wk Gel: Apply to affected areas bid for 4 wk |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Discontinue if sensitivity or irritation occurs; for external use only; avoid contact with eyes |
| Drug Name | Terbinafine (Lamisil) |
|---|---|
| Description | Inhibits squalene epoxidase, which decreases ergosterol synthesis, causing death of fungal cells. Use until symptoms significantly improve. Duration of treatment should be >1 wk but not >4 wk. |
| Adult Dose | Cream: Apply bid 1-4 wk Spray: Apply bid (morning and night) for 1 wk |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Discontinue if sensitivity or irritation occurs; for external use only; avoid contact with eyes |
Sometimes classified as a subset of allylamines. Useful for treating patients with refractory tinea pedis (eg, chronic hyperkeratotic). Have been shown to be effective in some patients with interdigital tinea pedis with only 1 wk of treatment.
| Drug Name | Butenafine 1% cream (Mentax) |
|---|---|
| Description | Damages fungal cell membranes, arresting growth of fungal cells. |
| Adult Dose | Apply bid for 1 wk or apply topically to affected area qd for 4 wk |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | For external use only; discontinue if irritation or sensitivity develops |
Should be considered in patients with extensive chronic hyperkeratotic or inflammatory/vesicular tinea pedis. Could also be used for patients with disabling disease, patients in whom topical treatments have failed, patients with diabetes or peripheral vascular disease, and patients with immunocompromising conditions.
| Drug Name | Itraconazole (Sporanox) |
|---|---|
| Description | Fungistatic activity. Synthetic triazole antifungal agent that slows fungal cell growth by inhibiting cytochrome P-450–dependent synthesis of ergosterol, a vital component of fungal cell membranes. |
| Adult Dose | 200 mg PO qd for 1 wk; not to exceed 400 mg/d; increase in 100-mg increments if no improvement (administer >200 mg/d in divided doses) |
| Pediatric Dose | Not established; suggested dose of 100 mg/d for systemic fungal infections |
| Contraindications | Documented hypersensitivity; coadministration with terfenadine (withdrawn from US market), astemizole (withdrawn from US market), triazolam, simvastatin, cisapride, quinidine, pimozide (withdrawn from US market), and HMG-CoA reductase inhibitors may cause adverse cardiovascular effects (possibly death) |
| Interactions | Antacids may reduce absorption; edema may occur with coadministration of calcium channel blockers (eg, amlodipine, nifedipine); hypoglycemia may occur with sulfonylureas; may increase tacrolimus and cyclosporine plasma concentrations when high doses are used; rhabdomyolysis may occur with coadministration of HMG-CoA reductase inhibitors (eg, lovastatin, simvastatin); coadministration with cisapride can cause cardiac rhythm abnormalities and death; may increase digoxin levels; coadministration may increase plasma levels of midazolam or triazolam; phenytoin and rifampin may reduce levels (phenytoin metabolism may be altered) |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Monitor hepatic function in patients taking itraconazole for >1 mo and in patients who develop any sign of hepatic insufficiency |
| Drug Name | Terbinafine (Lamisil, Daskil) |
|---|---|
| Description | Inhibits squalene epoxidase, which decreases ergosterol synthesis, causing death of fungal cells. Use until symptoms significantly improve. |
| Adult Dose | 250 mg PO qd for 1-2 wk |
| Pediatric Dose | Weight-based dosing 12-20 kg: 62.5 mg/d PO 20-40 kg: 125 mg/d PO >40 kg: 250 mg/d PO Treatment duration as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | May decrease cyclosporine effects; toxicity may increase with rifampin and cimetidine |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Perform hepatic function tests and CBC counts when taking for >6 wk, if signs of hepatic dysfunction develop, or if immunocompromised; not recommended for patients with preexisting liver disease or renal impairment |
| Drug Name | Fluconazole (Diflucan) |
|---|---|
| Description | Synthetic oral antifungal (broad-spectrum bistriazole) that selectively inhibits fungal cytochrome P-450 and sterol C-14 alpha-demethylation. |
| Adult Dose | 150 mg PO qwk for up to 4 wk |
| Pediatric Dose | 6 mg/kg/d PO for 2-3 wk |
| Contraindications | Documented hypersensitivity |
| Interactions | Levels may increase with coadministration of hydrochlorothiazide; levels may decrease with long-term coadministration of rifampin; coadministration of fluconazole may decrease phenytoin clearance; may increase concentrations of theophylline, tolbutamide, glyburide, and glipizide; effects of anticoagulants may increase with coadministration of fluconazole; increases in cyclosporine concentrations may occur when administered concurrently |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Monitor closely if rash develops and discontinue drug if lesions progress; may cause clinical hepatitis, cholestasis, and fulminant hepatic failure (including death) with underlying medical conditions (eg, AIDS, malignancy) and while taking multiple concomitant medications; not recommended in breastfeeding |
May use to supplement antimycotic agents in certain clinical situations.
| Drug Name | Aluminum acetate (Otic Domeboro, Burow's Solution) |
|---|---|
| Description | Drying agent for vesicular tinea pedis. Dissolve aluminum acetate tablets in water to produce a 1:10-40 solution. |
| Adult Dose | Soak feet bid; apply as a compress for 20-30 min 4-6 times/d until condition resolves |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | For external use only |
| Drug Name | Ammonium lactate lotion (Lac Hydrin) |
|---|---|
| Description | Used to decrease scaling in patients with hyperkeratotic soles. Contains lactic acid, an alpha hydroxy acid that has keratolytic action and thus facilitates release of comedones. Causes disadhesion of corneocytes. Available in 12% and 5% strengths. Use 12% lotion. |
| Adult Dose | Apply liberally to all affected areas bid until condition resolves |
| Pediatric Dose | Apply as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | May cause pain if applied on broken skin; may cause irritation with erythema, burning, and peeling if applied to face in 12% concentration |
| Drug Name | Urea, topical (Carmol-40, Keralac) |
|---|---|
| Description | Used to decrease scaling in patients with hyperkeratotic soles. Promotes hydration and removal of excess keratin by dissolving the intracellular matrix. Available in 10-40% concentration. |
| Adult Dose | Apply to all affected areas bid |
| Pediatric Dose | Apply as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | For external use only |
The need for follow-up care should be assessed on a case-by-case basis. Further outpatient visits may be indicated, depending on the extent and severity of the infection. Treatment regimens may need to be switched or augmented.
See Medication.
See Patient Education.
Secondary cellulitis, lymphangitis, pyoderma, and even osteomyelitis can result from mycotic infections of the feet. These complications are seen more frequently in patients with conditions such as chronic edema, immunosuppression, and diabetes.
The type of tinea pedis infection and underlying conditions (eg, immunosuppression, diabetes) affect the prognosis; however, with appropriate treatment, the prognosis is generally good.
Patients should be educated that reinfection can occur if they are reexposed to dermatophytes. Old shoes are often sources of reinfection and should be disposed of or treated with antifungal powders.
Patients should be cautioned to wear protective footwear at communal pools and baths and should attempt to keep their feet dry by limiting occlusive footwear. When occlusive footwear is worn, wearing cotton socks and adding a drying powder with antifungal action in the shoes may be helpful.
For excellent patient education resources, visit eMedicine's Foot Care Center. In addition, see eMedicine's patient education articles Athlete's Foot and Ringworm on Body.
Because tinea pedis is not associated with significant mortality or morbidity, the risk of medicolegal liability is slight. Secondary cellulitis, lymphangitis, and pyoderma can result from complications of mycotic infections of the feet, and practitioners must provide appropriate treatment in such cases.
Article Last Updated: Sep 5, 2007