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Author: Jacek C Szepietowski, MD, PhD, Professor and Vice-Head, Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Poland

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: Bernice R Krafchik, MBChB, FRCPC, Professor Emeritus, Department of Pediatrics, Section of Dermatology, University of Toronto; David F Butler, MD, Professor of Dermatology, Texas A&M University College of Medicine; Director, Division of Dermatology, Scott and White Clinic; Director Dermatology Residency Training Program, Scott and White Clinic; Van Perry, MD, Assistant Professor, Department of Medicine, Division of Dermatology, University of Texas Health Science Center; 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: ringworm, ringworm of the face, facial ringworm, superficial dermatophyte infection, glabrous skin, tinea barbae, keratinophilic fungus, dermatophyte, Microsporum canis, M canis, Trichophyton mentagrophytes, T mentagrophytes, Trichophyton rubrum, T rubrum, Trichophyton tonsurans, T tonsurans

Background

Tinea faciei is a superficial dermatophyte infection limited to the glabrous skin of the face. In pediatric and female patients, the infection may appear on any surface of the face, including the upper lip and chin. In men, the condition is known as tinea barbae when a dermatophyte infection of bearded areas occurs.

Pathophysiology

Keratinophilic fungi, or dermatophytes, are responsible tinea faciei. Dermatophytes release several enzymes, including keratinases, which allow them to invade the stratum corneum of the epidermis. Infection caused by zoophilic dermatophytes is usually associated with inflammatory reactions that are more severe than those due to anthropophilic fungi.

Frequency

International

Tinea faciei is not an uncommon disease. It occurs worldwide. However, as with other cutaneous fungal infections, it is more common in tropical regions with high temperatures and humidity. Recently, tinea faciei was shown to represent approximately 19% of all superficial fungal infections in the pediatric population with dermatomycoses.

Mortality/Morbidity

Scarring may occur in patients with Trichophyton schoenleinii infection; this is extremely rare.

Sex

Some authors suggest that females may be affected more frequently than males, but the difference is probably semantic. In females, dermatophyte infection of the face is more likely to be diagnosed as tinea faciei, whereas many infections that occur in similar locations in men are diagnosed as tinea barbae. Recent data indicate a female-to-male ratio of 1.06:1.

Age

Tinea faciei may appear in persons of any age, with 2 peaks of disease incidence. One peak involves children, who constitute a large group of patients because of their frequent direct contact with pets. Tinea faciei is commonly noted as a dermatosis that occurs after holidays; it is diagnosed more frequently in children after they spend their holidays in rural areas, where they may come into contact with animals when they play. Several cases are also reported in neonates; these patients may acquire the infection from siblings or contact with pets. The other peak occurs in those aged 20-40 years.



History

  • The infection is frequently acquired from pets in the home, but it can also be spread from individuals with dermatophyte infection elsewhere on the body.
  • Tinea faciei may resemble other dermatoses, such as cutaneous lupus erythematosus, polymorphous light eruption, and allergic contact dermatitis (Meymandi, 2003).

Physical

  • Because of the complex anatomy of the face, atypical features are more frequently found on the glabrous skin than the typical patches of tinea corporis.
  • Single or multiple erythematous patches without annular structure often resemble other dermatoses; delayed or missed diagnosis may result.
  • Lesions are almost always pruritic.
  • Typical signs of dermatophyte infection of the glabrous skin, similar to those of tinea corporis, may be present. These signs include annular or serpiginous erythematous scaling patches with an active border composed of papules, vesicles, and/or crusts. The most common locations are the cheeks, followed by the nose, periorbital area, chin, and forehead. Some patients may have multiple lesions present in different areas of the face.
  • In as many as 70% of patients with tinea faciei, various other dermatoses are considered.
    • Tinea faciei is the most frequently misdiagnosed entity among cutaneous fungal infections.
    • The atypical clinical features and incognito presentations support the separation of this disease from tinea corporis.
    • Occasionally, tinea faciei may simultaneously occur with other forms of dermatophyte infections, especially tinea capitis and tinea corporis.

Causes

The causative agents vary according to geographic regions.

  • Generally, animal reservoirs of zoophilic dermatophytes, especially Microsporum canis, are global among pets and livestock.
  • In Asia, Trichophyton mentagrophytes and Trichophyton rubrum are common.
  • In contrast, in North America Trichophyton tonsurans is the main pathogen isolated.



Candidiasis, Cutaneous
Contact Dermatitis, Allergic
Contact Dermatitis, Irritant
Granuloma Annulare
Lupus Erythematosus, Acute
Lupus Erythematosus, Bullous
Lupus Erythematosus, Discoid
Lupus Erythematosus, Drug-Induced
Lupus Erythematosus, Subacute Cutaneous
Neonatal Lupus Erythematosus
Perioral Dermatitis
Pityriasis Alba
Pityriasis Rosea
Rosacea
Sarcoidosis
Seborrheic Dermatitis
Syphilis

Other Problems to be Considered

Aspergillus infections under applied tape in neonates
Demodex folliculitis
Lupus vulgaris (Occasionally, lupus vulgaris may be in the differential diagnosis of particularly deep-seated annular plaques.)



Lab Studies

  • Even in the best mycology laboratories, as many as 30% of culture results may be negative, particularly in chronic infections.
  • Mycologic investigation is essential in the diagnosis of tinea faciei. It includes direct microscopic examination for hyphal elements and culturing.
  • The collection of the surface scrapings is important for laboratory studies. The material should be obtained from the border of the lesions where the more severe inflammatory reaction occurs and where more fungal elements are present.
  • Direct microscopic examination is the easiest mycologic procedure.
    • Scrapings are placed in 10-20% potassium hydroxide (KOH) solution, usually with the addition of dimethyl sulfoxide (DMSO). The latter helps to dissolve background keratinocytes to enable visualization of the fungal elements.
    • After warming the slide for a short time, the specimen is examined with a light microscope.
    • Some authors suggest detection is enhanced with special stains, such as chlorazol black E, Parker blue-black ink, or Swartz-Lamkin stain.
  • Culturing allows the identification of the causative pathogen.
    • Culturing is performed routinely with Sabouraud agar and the addition of cycloheximide and chloramphenicol. These substances inhibit the growth of bacteria and other contaminants.
    • After 3-4 weeks of incubation, the final identification is based on morphologic and microscopic findings in the colonies.
  • Dermatophytes may be diagnosed by using special media for rapid detection. This media contains a color indicator that changes from yellow to red with the growth of dermatophytes after a few days of incubation.

Histologic Findings

Histologic examination may occasionally be useful for establishing the diagnosis, but it is usually unnecessary. Its pattern is variable, ranging from mild focal spongiosis to a chronic spongiotic psoriasiform dermatitis with a mixed dermal inflammatory infiltrate and fungi in the cornified layer (Meymandi, 2003). Routine histopathologic evaluation with hematoxylin-eosin staining may reveal cutaneous fungal elements, but periodic acid–Schiff (PAS) staining is recommended to facilitate visualization.

Hyphae may be detected in the stratum corneum of the epidermis. Infections with T rubrum or Trichophyton verrucosum may invade hairs and follicles. A mixed cellular inflammatory infiltrate is usually present in the papillary dermis, and neutrophils may extend into the horny layers above.



Medical Care

Most cases of tinea faciei are curable with topical antifungal agents. If a topical steroid has been applied, fungal folliculitis may be present. Fungal folliculitis requires systemic therapy.

  • The frequency of daily application and duration of the treatment depend on the active ingredients of the preparation.
  • Topical ciclopirox and terbinafine possess additional anti-inflammatory effects, which are especially important in the therapy for infections caused by zoophilic dermatophytes in which inflammatory reactions are usually prominent.
  • Topical azoles are effective.
  • Although rare, chronic and/or multiple lesions may require systemic therapy.



The 2 classes of antifungal medication most commonly used to treat tinea faciei in practice are azoles and allylamines. Azoles inhibit lanosterol 14-alpha-demethylase, an enzyme that converts lanosterol to ergosterol, an important component of the fungal cell wall. Membrane damage leads to permeability problems and renders the fungus unable to reproduce. Allylamines inhibit squalene epoxidase, an enzyme that converts squalene to ergosterol; this inhibition also leads to the accumulation of toxic levels of squalene in the cell and to cell death. Several antifungal products from both classes are available for topical and systemic administration.

Re-evaluation of the tinea diagnosis is important if clinical improvement is not observed after 4 weeks of therapy.

Drug Category: Antifungal agents

With these agents, the mechanism of action may involve an alteration in cell membrane permeability, DNA or RNA synthesis, or intracellular levels of metabolites that are toxic to the fungal cell.

Drug NameButenafine (Mentax)
DescriptionPotent antifungal related to allylamines. Available as a 1% cream.
Adult DoseApply to affected areas qd for 2 wk
Pediatric Dose<12 years: Not established
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsUse topically (not in eyes, vagina, or other internal routes)

Drug NameClotrimazole (Lotrimin, Mycelex)
DescriptionBroad-spectrum antifungal agent that inhibits yeast and fungal growth by altering cell membrane permeability. Frequently prescribed for patients with tinea faciei. Available without a prescription as 1% cream, solution or spray, and lotion.
Adult DoseGently massage into affected area and surrounding skin areas bid for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsNot for treatment of systemic fungal infections; avoid contact with the eyes; if irritation or sensitivity develops, discontinue use and initiate appropriate therapy

Drug NameMiconazole (Femizole-7, Micatin, Absorbine)
DescriptionDamages fungal cell-wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased; this effect causes nutrients to leak out. Available as 2% cream, solution or spray, lotion, and powder. Lotion is preferred for use in intertriginous areas. If cream is used, apply sparingly to avoid maceration effects.
Adult DoseApply to affected areas bid for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsDiscontinue if sensitivity or chemical irritation occurs; for external use only; avoid contact with eyes

Drug NameEconazole (Spectazole)
DescriptionEffective in cutaneous infections. Interferes with RNA and protein synthesis and metabolism. Disrupts fungal cell wall permeability, causing fungal cell death.
Adult DoseApply to affected areas qd for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsDiscontinue if sensitivity or irritation develops; for external use only; avoid contact with eyes

Drug NameOxiconazole (Oxistat)
DescriptionDamages fungal cell-wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased causing nutrients to leak out. Available as a 1% cream or lotion.
Adult DoseApply to affected area qd for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsDiscontinue if sensitivity or chemical irritation; for external use only; avoid contact with the eyes

Drug NameUndecylenic acid (Desenex, Cruex, Fungoid AF, Gordochom)
DescriptionNonprescription agent rarely used in the treatment of tinea faciei. Available in cream or solution or spray.
Adult DoseApply to affected areas tid for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsFor external use only

Drug NameTolnaftate (Absorbine, Aftate, Breeze, Dr. Scholl's Athlete's Foot)
DescriptionNonprescription medication available in 1% cream, solution or spray, and powder.
Adult DoseApply to affected areas bid for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsFor external use only

Drug NameHaloprogin (Halotex)
DescriptionAgent for use in the treatment of superficial cutaneous infections. Available in 1% cream and solution or spray.
Adult DoseApply to affected areas bid for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsFor external use only

Drug NameCiclopirox (Loprox)
DescriptionInterferes with synthesis of RNA, DNA, and proteins by inhibiting transport within fungal cells. Available as a 1% cream and lotion for skin.
Adult DoseApply to affected areas bid for 3-4 wk
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsAvoid contact with eyes and other internal routes

Drug NameTerbinafine (Lamisil, Daskil)
DescriptionMember of allylamine family, fungicidal agents that inhibit ergosterol synthesis by means of squalene epoxidase. Result is a decreased ergosterol level and accumulation of squalene, which is toxic to fungal cells.
Adult Dose250 mg tab PO qd for 1-2 wk
Non-prescription cream: Apply to affected area bid for 2 wk
Pediatric Dose12-20 kg: 62.5 mg/d PO
20-40 kg: 125 mg/d PO
>40 kg: 250 mg/d PO for 1-2 wk as in adults
Cream: Administer as in adults
Consider longer therapy in Microsporum infections
ContraindicationsDocumented hypersensitivity
InteractionsMay decrease cyclosporine effects; toxicity may increase with rifampin and cimetidine
PregnancyB - Usually safe but benefits must outweigh the risks.
PrecautionsDiscontinue topical use if chemical irritation develops; discontinue oral therapy if hepatobiliary dysfunction, neutropenia, Stevens-Johnson syndrome, or changes in ocular lens or retina develop; pretreatment liver function and repeat LFTs evaluation required with oral treatment > 6 wk; dysgeusia and bone marrow abnormalities rare

Drug NameItraconazole (Sporanox)
DescriptionFungistatic 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. Best results are noted 2-3 wk after treatment.
Adult Dose100 mg PO qd for 2 wk; 200 mg PO qd for 1 wk; not to exceed 400 mg/d; increase in 100-mg increments if no improvement (>200 mg/d in divided doses)
Pediatric Dose3-5 mg/kg/d PO for 1-2 wk
ContraindicationsDocumented hypersensitivity
InteractionsAffects metabolism of drugs processed by cytochrome P450-3A enzyme system; antacids may reduce absorption; edema may occur with coadministration of calcium-channel blockers (eg, amlodipine, nifedipine); hypoglycemia may occur with sulfonylureas; high doses may increase tacrolimus and cyclosporine plasma concentrations; 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)
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in hepatic insufficiency

Drug NameFluconazole (Diflucan)
DescriptionFungistatic activity. Synthetic oral antifungal (ie, broad-spectrum bistriazole) that selectively inhibits fungal cytochrome P-450 and sterol C-14 alpha-demethylation. This inhibition prevents the conversion of lanosterol to ergosterol, thereby disrupting cellular membranes.
Adult Dose100 mg PO qd for 1-2 wk
Pediatric Dose3-6 mg/kg/d PO for 1-2 wk; FDA approved for use in children > 6 mo
ContraindicationsDocumented hypersensitivity
InteractionsHydrochlorothiazide may increase levels; levels may decrease with chronic coadministration of rifampin; coadministration may decrease phenytoin clearance; may increase concentrations of theophylline, tolbutamide, glyburide, and glipizide; anticoagulant effects may increase with coadministration; cyclosporine concentrations may increase when administered concurrently; use with cisapride may result in cardiac dysrhythmia
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsAdjust dose in renal insufficiency; monitor closely if rashes develop; discontinue if lesions progress; may cause clinical hepatitis, cholestasis, and fulminant hepatic failure (including death) with underlying medical conditions (eg, AIDS, malignancy) or with multiple concomitant medications; not recommended for use in breastfeeding women

Drug NameGriseofulvin (Fulvicin P/G, Gris-PEG)
DescriptionFungistatic activity. Interferes with microtubule impairs fungal cell division. Binds to keratin precursor cells. Keratin is gradually replaced with noninfected tissue, which is highly resistant to fungal invasions.
Adult Dose500 mg microsize or 330-375 mg ultramicrosize PO qd or divided bid for 3 wk
Pediatric Dose15-20 mg/kg/d microsize PO or 10-15 mg/kg/d ultramicrosize PO for 3 wk with fatty food or milk
ContraindicationsDocumented hypersensitivity; hepatic injury
InteractionsMay decrease hypoprothrombinemic activity of warfarin; may affect effectiveness of contraceptives; may reduce effects of cyclosporine; may decrease serum salicylate concentrations; barbiturates may decrease serum levels
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsIn prolonged therapy, observe patients closely; monitor renal, hepatic, and hematopoietic function regularly; lupus-like syndromes or exacerbation of lupus erythematosus may occur; photosensitivity may also occur (use protective measures against exposure to ultraviolet light or sunlight)



Deterrence/Prevention:

  • The isolation and treatment of infected pets is of great importance.

Prognosis:

  • The prognosis for patients with tinea faciei is usually good.
  • The lesions respond to topical and oral antifungal treatment within 4-6 weeks.

Patient Education:



Medical/Legal Pitfalls

  • Failure to properly diagnose.
    • Tinea faciei may be misdiagnosed as discoid lupus erythematosus, seborrheic dermatitis, rosacea, or contact dermatitis.
    • Tinea faciei is the most frequently misdiagnosed entity among cutaneous fungal infections. The atypical clinical features and incognito presentations support the separation of this disease from tinea corporis. Occasionally, tinea faciei may simultaneously occur with other forms of dermatophyte infections, especially tinea capitis and tinea corporis.



Media file 1:  Multiple lesions on the face caused by Microsporum canis infection in a patient who also has tinea capitis.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 2:  Erythematous scaling lesion on the cheek.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo



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Tinea Faciei excerpt

Article Last Updated: Feb 1, 2007