You are in: eMedicine Specialties > Dermatology > FUNGAL INFECTIONS Tinea CrurisArticle Last Updated: May 20, 2008AUTHOR AND EDITOR INFORMATIONAuthor: Michael Wiederkehr, MD, Consulting Staff, Livingston Dermatology Associates; Consulting Staff, Comprehensive Dermatology and Laser Center Michael Wiederkehr is a member of the following medical societies: Alpha Omega Alpha and American Medical Association Coauthor(s): Robert A Schwartz, MD, MPH, Professor and Head of Dermatology, Professor of Medicine, Professor of Pediatrics, Professor of Pathology, Professor of Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School 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; Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA; Lester F Libow, MD, Dermatopathologist, South Texas Dermatopathology Laboratory; Glen H Crawford, MD, Assistant Clinical Professor, Department of Dermatology, University of Pennsylvania School of Medicine; Chief, Division of Dermatology, The Pennsylvania Hospital; Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center Author and Editor Disclosure Synonyms and related keywords: tinea inguinalis, groin dermatophytosis, ringworm of the groin, gym itch, eczema marginatum, dhobie itch, jock itch, crotch rot, Trichophyton rubrum, T rubrum, Epidermophyton floccosum, E floccosum, Trichophyton mentagrophytes, T mentagrophytes, Trichophyton verrucosum, T verrucosum INTRODUCTIONBackgroundTinea cruris, a pruritic superficial fungal infection of the groin and adjacent skin, is the second most common clinical presentation for dermatophytosis. Tinea cruris is a common and important clinical problem that may, at times, be a diagnostic and therapeutic challenge. PathophysiologyThe most common etiologic agents for tinea cruris include Trichophyton rubrum and Epidermophyton floccosum; less commonly Trichophyton mentagrophytes and Trichophyton verrucosum are involved. Tinea cruris is a contagious infection transmitted by fomites, such as contaminated towels or hotel bedroom sheets, or by autoinoculation from a reservoir on the hands or feet (tinea manuum, tinea pedis, tinea unguium). The etiologic agents produce keratinases, which allow invasion of the cornified cell layer of the epidermis. The host immune response may prevent deeper invasion. Risk factors for initial infection or reinfection include wearing tight-fitting or wet clothing or undergarments. FrequencyUnited StatesDermatophytosis accounts for approximately 10-20% of all visits to dermatologists. InternationalTinea cruris has a worldwide distribution but is found more commonly in hot humid climates. Mortality/MorbidityNo mortality is associated with tinea cruris. Associated pruritus leads to morbidity resulting from lichenification, secondary bacterial infection, and irritant and allergic contact dermatitis caused by topically applied medications. SexTinea cruris is 3 times more common in men than in women. AgeAdults are affected much more commonly than are children. CLINICALHistoryPatients complain of pruritus and rash in the groin. A history of previous episodes of a similar problem usually is elicited. Additional historical information may include recently visiting a tropical climate, wearing tight-fitting clothes (including bathing suits) for extended periods, sharing clothing with others, participating in sports, or coexisting diabetes mellitus or obesity. Prison inmates, members of the armed forces, members of athletic teams, and people who wear tight clothing may be subject to independent or additional risk for dermatophytosis. PhysicalTinea cruris manifests as a symmetric erythematous rash in the groin.
CausesThe dermatophyte T rubrum is the most common etiologic agent for tinea cruris. In a Brazilian series, T rubrum was the prevalent dermatophyte in 90% of the cases, followed by T tonsurans (6%) and T mentagrophytes (4%).1 Other organisms, including E floccosum and T verrucosum, cause an identical clinical condition. T rubrum and E floccosum infections are more apt to become chronic and noninflammatory, while infection by T mentagrophytes often is associated with an acute inflammatory clinical presentation. DIFFERENTIALSAcanthosis Nigricans Candidiasis, Cutaneous Contact Dermatitis, Allergic Contact Dermatitis, Irritant Erythrasma Familial Benign Pemphigus (Hailey-Hailey Disease) Folliculitis Intertrigo Psoriasis, Plaque Seborrheic Dermatitis
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Drug Name | Terbinafine (Lamisil) |
|---|---|
| Description | Synthetic allylamine derivative, which inhibits squalene epoxidase, a key enzyme in sterol biosynthesis in fungi that results in a deficiency of ergosterol, causing fungal cell death. Widely studied and effective topical or oral antifungal. Topical form available without prescription. Some clinicians reserve this drug for more widespread/resistant infections because of its broad coverage and increased cost. Studies have found this medication to be effective and well tolerated in children. |
| Adult Dose | Topical: Apply to affected area qd for 1-4 wk Oral: 250 mg/d for 2 wk |
| Pediatric Dose | Topical: Administer as in adults Oral treatment based on body weight: 12-20 kg: 62.5 mg/d for 2 weeks 20-40 kg: 125 mg/d for 2 weeks >40 kg: 250 mg/d for 2 weeks |
| Contraindications | Documented hypersensitivity |
| Interactions | When administered concurrently with cyclosporine, oral administration of terbinafine may increase cyclosporine clearance; conversely, rifampin may decrease terbinafine clearance; cimetidine may decrease terbinafine clearance |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Discontinue if symptoms or signs of hepatobiliary dysfunction or cholestatic hepatitis develop or if chemical irritation occurs; topical dosage form is for external use only; avoid contact with eyes |
| Drug Name | Butenafine (Mentax) |
|---|---|
| Description | Potent antifungal related to the allylamines. Damages fungal cell membranes causing fungal cell growth to arrest. Available in 1% cream only. |
| Adult Dose | Apply topically to affected area qd for 2-4 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 | Use topically (not in eyes, vagina, or other internal routes) |
| Drug Name | Clotrimazole (Lotrimin, Mycelex) |
|---|---|
| Description | Often, first-line drug used in the treatment of tinea cruris. 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. Available without a prescription. 1% cream, solution/spray, and lotion available. |
| Adult Dose | Gently massage into affected area and surrounding skin 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 | Not for treatment of systemic fungal infections; avoid contact with the eyes; if irritation or sensitivity develops, discontinue use and institute appropriate therapy |
| Drug Name | Miconazole (Micatin, Monistat-Derm) |
|---|---|
| Description | Damages fungal cell wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased causing nutrients to leak, resulting in fungal cell death. Available without a prescription, and 2% cream, solution/spray, lotion, and powder forms available. Lotion is preferred in intertriginous areas. If cream is used, apply sparingly to avoid maceration effects. |
| Adult Dose | Cream and lotion: Cover affected areas bid for 4 wk Powder: Spray or sprinkle liberally over affected area 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 chemical irritation occurs; for external use only; avoid contact with eyes |
| Drug Name | Ketoconazole (Nizoral) |
|---|---|
| Description | 2% cream. Imidazole broad-spectrum antifungal agent; inhibits synthesis of ergosterol, causing cellular components to leak, resulting in fungal cell death. |
| Adult Dose | Rub gently into affected area qd or 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 irritation develops; for external use only; avoid contact with eyes |
| Drug Name | Econazole (Spectazole) |
|---|---|
| Description | Effective in cutaneous infections. Interferes with RNA and protein synthesis and metabolism. Disrupts fungal cell wall permeability, causing fungal cell death. |
| Adult Dose | Apply sparingly over affected area qd/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 irritation develops; for external use only; avoid contact with eyes |
| Drug Name | Naftifine (Naftin) |
|---|---|
| Description | Broad-spectrum antifungal agent and synthetic allylamine derivative; may decrease the synthesis of ergosterol, which in turn inhibits fungal cell growth Available in 1% cream or solution. If no clinical improvement after 4 wk, reevaluate patient. |
| Adult Dose | Cream/gel: Gently massage sparingly into affected area and surrounding skin qd for 2-4 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 use if sensitivity or chemical irritation occurs; for external use only; avoid contact with eyes |
| Drug Name | Oxiconazole (Oxistat) |
|---|---|
| Description | Broad-spectrum antifungal agent. Inhibits synthesis of ergosterol, causing cellular components to leak, resulting in fungal cell death. 1% cream or lotion. |
| Adult Dose | Apply topically to affected area qd for 2-4 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 |
| Drug Name | Tolnaftate (Tinactin) |
|---|---|
| Description | Nonprescription medication used in the treatment of tinea cruris. Available in 1% cream, solution/spray, and powder. |
| Adult Dose | Apply topically bid |
| 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 | Haloprogin (Halotex) |
|---|---|
| Description | Agent for use in the treatment of tinea cruris. Prescription only. Available in 1% cream and solution/spray. |
| Adult Dose | Apply topically tid |
| 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 | For external use only |
| Drug Name | Ciclopirox (Loprox) |
|---|---|
| Description | Synthetic broad-spectrum antifungal agent. Interferes with synthesis of DNA, RNA, and protein by inhibiting the transport of essential elements in fungal cells. Prescription only. Available in 1% cream and lotion. |
| Adult Dose | Massage into affected areas bid; reevaluate diagnosis if no improvement after 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 | For external use only; avoid contact with eyes and other internal routes |
| Drug Name | Itraconazole (Sporanox) |
|---|---|
| Description | Fungistatic activity. Synthetic triazole antifungal agent that slows fungal cell growth by inhibiting cytochrome P450-dependent synthesis of ergosterol, a vital component of fungal cell membranes. Widely used and well-studied oral antifungal that can be used in the treatment of tinea cruris. Studies have shown that it is tolerated better than griseofulvin. Best results are noted 2-3 wk after the end of treatment. |
| 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 | 5 mg/kg/d PO for 1 wk |
| Contraindications | Documented hypersensitivity; may not be taken in conjunction with cisapride, midazolam, triazolam, and lovastatin |
| Interactions | Avoid alcohol because disulfiramlike reactions may occur; antacids may reduce absorption; rhabdomyolysis may occur with coadministration of HMG-CoA reductase inhibitors; coadministration with cisapride may cause cardiac arrhythmia; coadministration with midazolam or triazolam may increase their plasma levels |
| 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 | Adverse effects include headache, nausea, vomiting, reversible elevation of liver enzymes, hepatotoxicity, hallucinations, hypokalemia, and edema |
| Drug Name | Sulconazole (Exelderm) |
|---|---|
| Description | Broad-spectrum antifungal agent. Inhibits synthesis of ergosterol, causing cellular components to leak, resulting in fungal cell death. 1% cream or solution. |
| Adult Dose | Apply topically to affected area qd for 2-4 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 external use only; avoid contact with eyes and other internal routes |
| Drug Name | Griseofulvin (Fulvicin-U/F, Grifulvin-V) |
|---|---|
| Description | Fungistatic activity. Fungal cell division is impaired by interfering with microtubule. Binds to keratin precursor cells. Keratin gradually is replaced by noninfected tissue, which is highly resistant to fungal invasions. Less effective than itraconazole in treatment of tinea cruris. |
| Adult Dose | 500 mg microsize (330-375 mg ultramicrosize) PO qd or divided bid for 2-4 wk |
| Pediatric Dose | 10-25 mg/kg/d PO; 20 mg microsize/kg/d (5 mg/lb/d) PO or 7.3 mg ultramicrosize/kg/d (3.3 mg/lb/d) PO |
| Contraindications | Documented hypersensitivity; do not administer with cisapride |
| Interactions | Avoid alcohol because disulfiramlike reactions may occur; intense UV light exposure may result in phototoxic reactions; may decrease hypoprothrombinemic activity of warfarin; contraceptives may lose effectiveness; may reduce effects of cyclosporine; may decrease serum salicylate concentrations; barbiturates may decrease serum griseofulvin levels |
| 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 | On prolonged therapy, observe patients closely; monitor renal, hepatic, and hematopoietic function regularly; lupuslike syndromes or exacerbation of lupus erythematosus may occur; photosensitivity may occur; therefore advise patients to take protective measures against exposure to UV light or sunlight |
| Media file 1: Tinea cruris. | |
![]() | View Full Size Image | Media type: Photo |
| Media file 2: Tinea cruris. | |
![]() | View Full Size Image | Media type: Photo |
| Media file 3: Tinea cruris. | |
![]() | View Full Size Image | Media type: Photo |
| Media file 4: Tinea cruris (hematoxylin and eosin stain). | |
![]() | View Full Size Image | Media type: Image |
| Media file 5: Tinea cruris (periodic acid-Schiff stain, magnification X 20). | |
![]() | View Full Size Image | Media type: Photo |
| Media file 6: Tinea cruris (Gomori methenamine-silver stain, magnification X 20). | |
![]() | View Full Size Image | Media type: Photo |
Article Last Updated: May 20, 2008