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Author: Noah S Scheinfeld, MD, JD, FAAD, Assistant Clinical Professor, Department of Dermatology, Columbia University; Consulting Staff, Department of Dermatology, St Luke's Roosevelt Hospital Center, Beth Israel Medical Center, New York Eye and Ear Infirmary; Private Practice

Noah S Scheinfeld is a member of the following medical societies: American Academy of Dermatology

Coauthor(s): Matthew C Lambiase, DO, Staff Physician, Department of Dermatology, Brooke Army Medical Center; Daniel S Lehman, MD, Fellow in Minimally Invasive Urology/Oncology, Department of Urology, Columbia University Medical Center; Jessica M Allan, MD, Consulting Staff, Private Practice

Editors: Franklin Flowers, MD, Chief, Division of Dermatology, Professor, Department of Medicine and Otolaryngology, University of Florida College of Medicine; Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA; Paul Krusinski, MD, Director of Dermatology, Professor, Department of Internal Medicine, Fletcher Allen Health Care, University of Vermont; 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: yeast, candidosis, vulvovaginitis, balanitis, intertrigo, paronychia, onychomycosis, erosio interdigitalis blastomycetica

Background

Yeasts are unicellular fungi that typically reproduce by budding, a process that entails a progeny pinching off of the mother cell. Candidosis is an infection caused by the yeast Candida albicans or other Candida species. C albicans, the principal infectious agent in human infection, is an oval yeast 2-6 µm in diameter. C albicans (as well as most medically significant fungi) has the ability to exist in both hyphal and yeast forms (termed dimorphism). If pinched cells do not separate, a chain of cells is produced and is termed pseudohyphae.

Superficial infections of skin and mucous membranes are the most common types of candidal infections of the skin. Common types of candidal skin infection include intertrigo, diaper dermatitis, erosio interdigitalis blastomycetica, perianal dermatitis, and candidal balanitis. In certain subpopulations, candidal infection of the skin has increased in prevalence in recent years, principally because of the increased numbers of patients who are immunocompromised.

Esophagitis, septicemia, endocarditis, peritonitis, and urinary tract infections are less frequent types of candidosis. Although C albicans is the most common cause of human infection, the genus Candida includes more than 150 species. Candida tropicalis, Candida parapsilosis, Candida guilliermondi, Candida krusei, Candida kefyr, Candida zeylanoides, and Candida glabrata (formerly Torulopsis glabrata) are less common causes of human disease.

Humans carry yeast fungi, including candidal species, throughout the gastrointestinal tract (mouth through anus) as part of the normal commensal flora. The vagina also commonly is colonized by yeast (13% of women), most commonly by C albicans and C glabrata. The commensal oral isolation of candidal species ranges from 30-60% in healthy adults. Note that Candida species are not part of the normal flora of the skin; however, they may colonize fingers or body folds transiently.

The eMedicine articles Candidiasis, Mucosal and Candidiasis may be of interest. Additionally, see the related Medscape CME courses The Changing Epidemiology of Candida Infections and New Directions in the Management of Invasive Fungal Infections in Neonatal and Pediatric Populations.

Pathophysiology

Most candidal species are known to produce virulence factors including protease factors. Those strains lacking virulence factors have been shown to be less pathogenic. The ability of yeast forms to adhere to the underlying epithelium is an important step in the production of hyphae and tissue penetration. Removal of bacteria from the skin, mouth, and gastrointestinal tract by exposing to tissue with its endogenous flora results in inhibition of endogenous microflora, providing reduced environmental and nutritional competition that favors the growth of candidal organisms.

Frequency

United States

Candida species are a common cause of intertrigo in both elderly and diabetic patients. Candida species currently are the fourth leading cause of bloodstream infections in the United States, with occurrence at a disproportionately high rate in persons aged 65 years and older.

International

A German study1 investigated the different causes of diaper dermatitis in 46 men and women at a median age of 85 years. In 38 patients, a cause was established; specifically, 63% had candidiasis, 16% had irritant dermatitis, 11% had eczema, and 11% had psoriasis. Of these patients, 37 were treated and 73% were cured after 8 weeks of treatment.

In Germany, Kränke et al2 studied 126 patients with a presumptive diagnosis of anal eczema (age range, 7-82 y), and most patients were male (57.1% male, 42.9% female). The clinical diagnosis was intertrigo/candidiasis in 42.9% of patients.

In Argentina, Nardin et al3 analyzed 2073 samples of skin, hair, nails, and oral mucous membranes obtained from 1817 patients who attended the Microbiology Branch of the Central Laboratory at Dr. J.M. Cullen Hospital from September 1999 to September 2003. The samples were examined and identified according to localization and the type of lesion. Of the total samples, 55.67% were positive; 63% were recovered from females and 37% were recovered from males. C albicans was the prevalent yeast species.

In Japan, Nishimoto4 noted that cutaneous candidiasis was seen in 755 (1%) of 72,660 outpatients. Intertrigo (347 cases) was the most common clinical manifestation of cutaneous candidiasis, erosio interdigitalis occurred in 103 cases, and diaper candidiasis was noted in 102 cases.

Mortality/Morbidity

Superficial candidal infections cause significant morbidity in older adults, which becomes a particular problem with the use of certain types of medication, poor self-care, and decreased salivary flow. Age alone is not sufficient for the development of candidal infection; however, increased morbidity is associated with both superficial and invasive forms of disease. This is a result of an increased risk in patients of developing an underlying immunosuppressed state, such as malignancy.

Age

Neonatal cutaneous and systemic candidiasis have become increasingly prevalent in neonatal intensive care nurseries. Postnatal acquisition has been attributed to increased survival rates of low birth weight babies in association with an increased number of invasive procedures and widespread use of broad-spectrum antibiotics. Neonatal candidiasis presents 3-7 days after birth with oral thrush and diaper dermatitis. This has been attributed to mucosal contact with the organism during labor and delivery.

The number of candidal infections has risen dramatically in recent years, mirroring the increasing number of patients who are immunocompromised. Specifically, increased age appears to be associated with increased morbidity and mortality. Older adults are more likely to be exposed to situations that increase the risk of invasive candidiasis, including treatment with broad-spectrum antibiotics, hyperalimentation, and increased contact with invasive monitoring devices in an intensive care unit. Superficial candidal infections, although typically believed to be benign, cause significant morbidity in the elderly population.

Candidal infections are exacerbated by certain types of medication (eg, antibiotics), poor self-care, and decreased salivary flow, all of which often are associated with aging. In addition, treatment with cytotoxic agents (eg, methotrexate, cyclophosphamide) for dermatologic and rheumatic conditions or aggressive chemotherapy for malignancy in elderly patients puts them at higher risk.



History

  • Candidal vulvovaginitis: This common condition in women presents with itching, soreness, and a thick creamy white discharge (see Media File 1). Although most candidal infections occur more frequently with advancing age, vulvovaginitis is unusual in older women. In the absence of estrogen stimulation, the vaginal mucosa becomes thin and atrophic, producing less glycogen. Candidal colonization of vaginal mucosa is estrogen dependent and subsequently decreases sharply after menopause (see Media File 2). In contrast, the likelihood of colonization increases during pregnancy (25-33%). The widespread use of hormone replacement for reduction of osteoporosis and heart disease may cause an increasing trend in candidal vulvovaginitis among older women. Cutaneous hypersensitivity to C albicans has been reported in persons with idiopathic vulvodynia.5
  • Candidal balanitis: Signs and symptoms of this candidal infection vary but may include tiny papules, pustules, vesicles, or persistent ulcerations on the glans penis (see Media File 3). Exacerbations following intercourse are common.
  • Congenital candidosis6, 7: This rarely reported candidal infection (70 cases during the 1990s) may be acquired by the infant in utero or during delivery. Presumably, congenital candidosis is an ascending intrauterine infection with cutaneous or systemic manifestations that typically present within 12 hours after birth. Although the congenital systemic form typically is fatal, congenital cutaneous infections usually have a more benign course. Prematurity and the presence of an intrauterine foreign body (intrauterine device) are associated with this condition. Untreated, infants are at higher risk for systemic infection, which is associated with a high mortality rate (70%). Some infants have respiratory distress and pneumonia secondary to in utero aspiration of infected amniotic fluid.
  • Oropharyngeal candidiasis (OPC): This form is known more commonly as oral thrush and is considered by many to be a minor problem of little significance that may clear spontaneously. However, without appropriate treatment this can lead to a chronic condition that can result in discomfort and anorexia. Rarely, oropharyngeal infection leads to systemic candidiasis.
    • OPC in the neonate most commonly is acquired from the infected maternal mucosa during passage of the infant through the birth canal. OPC is 35 times more common in neonates of infected mothers compared to uninfected mothers.
    • OPC is the most common type of clinical presentation in infants and children. Immaturity of host defenses and incomplete establishment of the normal orointestinal flora are likely reasons why C albicans often acts as a pathogen in the neonate compared to a child aged several months who is not nearly as susceptible. Beyond the neonatal age, C albicans is considered a normal constituent of the oral and intestinal flora.
    • Candidosis of the nipple in the nursing mother is associated with infantile OPC. Nipple candidosis almost always is bilateral, with the nipples appearing bright red and inflamed, with the look and feel of being sunburned or on fire. Unlike a painful-with-nursing cut or abrasion from local trauma by the infant (incorrect latch-on), nipple candidosis hurts between feedings. Merely having the clothing brush against the nipples is painful.
  • Candidal diaper dermatitis (CDD): Infants with OPC invariably harbor C albicans in the intestine and feces (85-90%). In most patients, CCD is the result of progressive colonization from oral and gastrointestinal candidiasis. Infected stools represent the most important focus for cutaneous infection. Moist macerated skin is particularly susceptible to invasion by C albicans. Additional factors that predispose infants to CDD include local irritation of the skin by friction; ammonia from bacterial breakdown of urea, intestinal enzymes, and stool; detergents; and disinfectants.
  • Oral candidiasis in adults: Use of broad-spectrum antibiotics and inhaled corticosteroids, diminished cell-mediated immunity, and xerostomia are all risk factors for candidiasis (see Media File 4).
    • Xerostomia may be either primary resulting from the natural aging process or secondary resulting from the anticholinergic effect of certain drugs including psychoactive drugs such as phenothiazines and tricyclic antidepressants. A decrease in salivary production decreases both the amount of available mucosal secretory antibody (immunoglobulin A [IgA]) and the natural cleansing action provided by saliva.
    • In older adults, the development of oral thrush in the absence of a known etiology should raise the clinician's index of suspicion for an underlying cause of immunosuppression, such as malignancy or AIDS.
    • With denture stomatitis, the areas of erythema may be painful and may affect up to 65% of patients who wear dentures, especially those who wear full sets. Despite popular belief, denture stomatitis is not associated with smokers or patients who are immunosuppressed.
  • Intertrigo: Most cases of cutaneous candidosis occur in skin folds where occlusion (by clothing or shoes) produces abnormally moist conditions. Sites such as the perineum, mouth, and anus, in which Candida organisms normally may be carried, are at further risk of infection. Candidal infection of the skin under the breasts or pannus occurs when those areas become macerated (see Media File 5).
  • Decubital candidosis: This is a particular form of cutaneous candidosis that occurs on the dorsal skin of chronically bedridden patients.8
  • Paronychia: Candida organisms occasionally cause infection in the periungual area and underneath the nailbed (see Media File 6). Candida species (not always C albicans) can be isolated from most patients with chronic paronychia. The yeast is believed to play an etiologic role in this condition, but bacteria also may act as co-pathogens. Immediate contact dermatitis to food allergens may play a role in the pathogenesis of the condition as well. Progression to total nail dystrophy has been associated specifically with C albicans and usually has been limited to women with 2 important predisposing conditions, ie, Cushing syndrome and Raynaud disease. Disease is more common in people who frequently submerge their hands in water and usually is not associated with the elderly population. One important exception to this generalization is the population of patients with diabetes.
  • Candidosis and HIV: Epidemiologic studies indicate that a very high percentage of patients infected with HIV contract some type of skin disorder during the course of the disease. More specifically, most patients with HIV infection have some form of candidal infection during the illness. Recurrent episodes of oral candidiasis typically occur in patients in whom CD4 counts are less than 300/µL, an important marker of disease progression. Additionally, Yanagisawa et al,9 in 2007, reported on a case of disseminated candidiasis as an initial presentation of AIDS. Such cases often manifest with purpuric eruptions.
  • Chronic mucocutaneous candidiasis: See Candidiasis, Chronic Mucocutaneous for discussion of that form of candidiasis.
  • Breast pain: Andrews et al10 studied 98 breastfeeding women, 20 who reported breastfeeding associated pain and 78 who were asymptomatic. Cultures were obtained from breast milk, areolae, and the infants' oropharynx. Six of the 20 symptomatic women returned breast milk cultures positive for yeast, compared with 6 of 78 controls (11 of 12 samples showed C albicans). The researchers suggested that Candida might play an etiologic role in breastfeeding-associated pain.
  • Ecthyma gangrenosum: In 2007, Agarwal et al11 reported on a solitary ecthyma gangrenosum–like lesion that resulted from C albicans infection in a neonate.
  • Ulcers: Xi et al,12 in 2007, reported a 51-year-old Cantonese woman who had a 1-year history of a large, deep-seated subcutaneous ulcer on her right shoulder for more than a year whose discharge showed C albicans and C parapsilosis. The researchers isolated C parapsilosis from the biopsy specimen.

Physical

  • Candidal vulvovaginitis: Clinical examination reveals erythema of the vaginal mucosa and vulval skin with curdy white flecks within the discharge. Erythema may spread to include the perineum and groin, with satellite pustules. Alternatively, the vaginal mucosa may appear red and glazed. A patient presenting with symptoms of vulvovaginitis with identification of yeasts in the vaginal discharge has a diagnosis of candidosis.
  • Congenital candidosis: In 2004, Diana et al13 reported that cutaneous congenital candidiasis (CCC) is a rare disease of term or premature infants. It typically manifests as an erythematous maculopapular eruption affecting the trunk and extremities; it resolves after extensive desquamation. Pustules and vesicles usually are superficial and resolve spontaneously or with topical treatment (see Media File 8). The presence of white microabscesses on the placenta and umbilical cord of an infant with such an eruption must suggest the diagnosis of CCC. It is always secondary to candidal chorioamnionitis, but it may pass unrecognized.
  • OPC in the infant: Lesions become visible as pearly white patches on the mucosal surfaces. Buccal epithelium, gums, and the palate commonly are involved with extension to the tongue, pharynx, or esophagus in more severe cases. If the lesions are scraped away, an erythematous base is exposed. Lesions may progress to symptomatic erosion and ulceration.
  • Candidal diaper dermatitis: The eruption of CDD usually starts in the perianal area, spreading to involve the perineum and, in severe cases, the upper thighs, lower abdomen, and lower back. Maceration of the anal mucosa and the perianal skin often is the first clinical manifestation. The typical eruption begins with scaly papules that merge to form well-defined, weeping, eroded lesions with a scalloped border. A collar of overhanging scales and an erythematous base may be demonstrated. Satellite flaccid vesicopustules around the primary intertriginous plaque also are characteristic of CDD and represent the primary lesions.
  • Oral candidiasis in elderly persons: The most common clinical appearance of OPC (pseudomembranous candidosis or oral thrush) in the adult population occurs as white plaques that are present on the buccal, palatal, or oropharyngeal mucosa overlying areas of mucosal erythema. Typically, the lesions are removed easily and may demonstrate areas with tiny ulcerations (see Media File 7). In addition, some patients may develop soreness and cracks at the lateral angles of the mouth (angular cheilitis). Denture stomatitis presents as chronic mucosal erythema typically beneath the site of a denture.
  • Intertrigo: Intertrigo typically presents with erythema, cracking, and maceration with soreness and pruritic symptoms. Lesions typically have an irregular margin with surrounding satellite papules and pustules. Web spaces of affected fingers or toes are macerated and have the appearance of soft white skin, which is a condition termed erosio interdigitalis blastomycetica (interdigital candidosis).
  • Paronychia: The nailfold becomes erythematous, swollen, and tender, with an occasional discharge. Loss of the cuticle occurs, along with nail dystrophy and onycholysis with discoloration around the lateral nailfold (see Media File 9). A greenish color with hyponychial fluid accumulation may occur that results entirely from Candida, and not Pseudomonas, infection. A potassium hydroxide (KOH) preparation is helpful and is likely to show yeast organisms.

Causes

  • Host factors that predispose patients to infections are numerous. Local factors such as tissue damage resulting from trauma, xerostomia, radiation-induced mucositis, ulcerations, skin maceration, or occlusion enhances adhesion and predisposes patients to increased infection rates.
  • Endocrine diseases such as diabetes mellitus, Cushing syndrome, hypoparathyroidism, hypothyroidism, and polyendocrinopathy are associated with increased susceptibility to infection. The mechanism by which diabetes mellitus is believed to raise infection rates is through increased tissue glucose, altered yeast adhesion, and decreased phagocytosis.
  • Nutritional deficiencies may alter host defense mechanisms or epithelial barrier integrity, allowing increased adherence or penetration. Iron deficiency anemia and deficiencies including vitamins B1, B2, B6, C, and folic acid are associated with heightened infection rates.
  • T-lymphocyte–mediated immunity plays an important immunologic role against infection through phagocytosis and killing by polymorphonuclear cells and macrophages. Individuals with deficient T-lymphocyte function, such as patients with AIDS, appear to be particularly vulnerable to mucosal or cutaneous candidiasis but not to systemic infection. Patients with primary immune deficiencies, such as lymphocytic abnormalities, phagocytic dysfunction, IgA deficiency, viral-induced immune paralysis, and severe congenital immunodeficiencies, often are affected by OPC and other fungal mycoses.



Candidiasis, Mucosal
Intertrigo
Onychomycosis
Seborrheic Dermatitis

Other Problems to be Considered

Bacterial vaginosis
Contact dermatitis with or without colonization
Pseudomonas nailbed infection
Inverse psoriasis
Radiation dermatitis
Trichomonas infection



Lab Studies

  • KOH preparation is the easiest and most cost-effective method for diagnosing CCC, but its use is not sufficient in the absence of other supporting clinical evidence.
  • Culture from an intact pustule, skin biopsy tissue, or desquamated skin can help to support the diagnosis.
  • Microscopic examination of skin scrapings prepared with calcofluor white stain is a simple way of detecting yeasts and pseudohyphae of C albicans. C albicans binds nonspecifically to polysaccharides found in fungal cell walls and produces a distinct bright color in a pattern characteristic for the organism when viewed under a fluorescence microscope.
  • When a greenish hyponychial fluid accumulates, material may be obtained by heating a pin and painlessly puncturing the intact overlying nail. The fluid release provides symptomatic relief to the patient, and fluid may demonstrate multiple yeast organisms when viewed using KOH preparation.

Histologic Findings

A skin biopsy specimen stained with a periodic acid-Schiff stain reveals nonseptated hyphae. The presence of nonseptated hyphae allows cutaneous candidiasis to be distinguished from tinea.



Medical Care

  • Candidal vulvovaginitis: Topical antifungal agents including miconazole nitrate (Micatin, Monistat-Derm) or clotrimazole (Lotrimin, Mycelex) creams are curative. One-time oral therapy with fluconazole (150 mg) or itraconazole (600 mg) is effective and may be a more attractive alternative to some patients, but it is more costly.
  • Candidal balanitis: Topical therapy is sufficient in most patients. Evaluate asymptomatic sexual partners and treat them if they are affected. If persistent lesions spread beyond the genitalia, consider the possibility of diabetes, and assess for the disease.
  • Congenital candidosis: Topical preparations usually are effective. Some authors recommend the use of oral nystatin in conjunction with topical agents to lower the risk of systemic infection.
  • OPC in the infant: Most patients can be treated with nystatin oral suspension. Treat for 10-14 days or until 48-72 hours after resolution of symptoms. Dosage for preterm infants is 0.5 mL (50,000 U) to each side of mouth 4 times/day; dosage for infants is 1 mL (100,000 U) to each side of the mouth 4 times/d.
  • Candidosis of the nipple: Treat nipple candidosis for 2 weeks using an antifungal cream after each feeding. The baby must be treated simultaneously with nystatin swabbed on all 4 gum lines and in the oral cavity, along with a few ingested drops, for 2 weeks. Babies may have no symptoms of OPC and still be reinfecting their mothers. Careful hygiene is also important. Frequent changing and washing of bras in boiling water (along with anything the baby puts in its mouth, eg, pacifiers) is necessary. Gentian violet is not used because it stains badly and may irritate the infant's mouth. If candidosis of the nipple goes untreated, it may extend, and oral treatment for the mother may be necessary. Cultures often are not pure and usually are not helpful.
  • Candidal diaper dermatitis: Treatment for CDD includes practical measures that reduce the amount of time the diaper area is exposed to hot and humid conditions. Air drying, frequent diaper changes, and generous use of baby powders and zinc oxide paste are adequate preventive measures. For topical therapy of CDD, nystatin, amphotericin B, miconazole, and clotrimazole are effective and almost equivalent in efficacy.
  • Oral candidiasis in adults
    • Treatment with a topical agent such as nystatin (1:100,000 U/mL, 5 mL oral rinse and swallow qid) or clotrimazole troches (10 mg 5 times/d) usually is effective. In most patients, extend the duration of antifungal therapy at least twice as long as the termination of clinical signs and symptoms of candidosis. Reserve oral fluconazole, 100 mg once daily for 2 weeks, for patients with more severe disease.
    • With denture stomatitis, improved oral hygiene with removal of dentures at night, vigorous brushing to remove plaque, and disinfecting (swish and spit) with chlorhexidine gluconate (Peridex) usually is adequate treatment. Topical therapy with clotrimazole troches or nystatin may be used for lesions that do not respond to the above measures. For more resistant cases oral fluconazole, 100 mg/day for several weeks, in addition to the above measures, may prove effective.
  • Intertrigo
    • Treatment is targeted to keeping the skin dry, with the addition of topical nystatin powder, clotrimazole, or miconazole twice daily. Patients with extensive infection may require the addition of fluconazole (100 mg PO qd for 1-2 wk) or itraconazole (100 mg PO qd for 1-2 wk). Many anecdotally based remedies exist for intertrigo that have been used in dermatology offices for years with success. The remedies have focused on both drying the moist inflamed area and treating the candidosis. The treatments are adjusted based on whether the inflammation is acute (wet and red), subacute (red +/- maceration), or chronic (red and dry).
    • For acute intertrigo, use vinegar/water (1 tablespoon vinegar per quart of room temperature water) applied twice per day for 5-10 minutes for 3-5 days as needed. Dry the area with a hair dryer (no heat). Apply a shake lotion twice per day (mixture: 40 g USP talc, 40 g zinc oxide, 10 g glycerin; mix into slurry or milkshake consistency, add distilled water up to 120 mL, dispense in 180-mL [6 oz] bottle). Place a large bath towel under breasts or in pendulous areas twice per day. Castellani paint (carbol fuchsin) is messy, but nightly painting may help when nothing else does.
    • For subacute intertrigo, benzoyl peroxide wash may be used to cleanse the area instead of application of vinegar or Castellani paint. A topical anticandidal cream of choice is applied twice per day, with or without a mild hydrocortisone cream (no refills for the latter).
    • For chronic intertrigo, the zinc-talc shake lotion may be used once or twice daily, and the hydrocortisone cream/antifungal mixture may be applied at night. Local hyperhidrosis may be treated with antiperspirants (ie, Arrid Extra Dry Unscented, Dry Idea) on a long-term basis. These products, along with the more concentrated Drysol (aluminum chloride 20%), may sting macerated skin. Nystatin in talc (100,000 U/g or 15 g) may be applied twice per day for a few days, then tapered and replaced with unscented baby powder as a powder-approach alternative.
    • Sundaram et al14 noted that candidal intertrigo can be treated with filter paper soaked in Castellani paint.
  • Paronychia: Treatment with topical agents usually is not effective but should be tried for chronic candidal paronychia. Drying solutions or antifungal solutions are used. Oral therapy with either itraconazole (pulse dosing with 200 mg bid for 1 wk of each of 3 consecutive mo) or terbinafine (250 mg qd for 3 mo) is recommended.
  • Candidosis and HIV: Topical therapy with agents such as nystatin and clotrimazole require a minimum of 20-30 minutes of drug contact with the oral mucosa. Treatment with topical therapies may be effective in the early stages of HIV infection, and it becomes less effective with disease progression. Oral treatment with a 2-week course of antifungal therapy (itraconazole, fluconazole, ketoconazole) is indicated in more refractory cases. In patients who are significantly immunocompromised, maintenance therapy on an intermittent (alternate days to twice weekly dosing of ketoconazole 200 mg or fluconazole 100 mg) or continuous basis may be required to provide symptomatic relief. In general, the goal is the cessation of therapy once clinical symptoms have subsided, since prolonged therapy increases the likelihood of the development of drug-resistant organisms.



The azoles are a group of synthetic antimycotic agents with a broad spectrum of activity. The primary drugs available include ketoconazole, miconazole, fluconazole, itraconazole, and econazole. The mechanism of action of azoles is blocking the synthesis of ergosterol, the primary sterol in the fungal cell membrane. The depletion of ergosterol alters the fluidity of the cell membrane and alters the action of the membrane-associated enzymes. This results in inhibition of replication and inhibition of the transformation of candidal yeast forms into hyphae, which is the invasive and pathogenic form of the parasite.

Nystatin and amphotericin are polyenes, which are active against some fungi but have little action on mammalian cells and no action on bacteria. They bind to cell membranes and interfere with permeability and transport functions. These antibiotics act as ionophores and causes leakage of cations.

Terbinafine is an allylamine that is fungicidal for a wide range of skin pathogens. It inhibits squalene epoxidase, which is involved in the synthesis of ergosterol from squalene in the fungal cell wall. The accumulation of squalene within the cell is toxic to the organism.

A case of chronic mucocutaneous candidosis that was cured with micafungin has been reported.

Voriconazole is another third-line treatment.

Drug Category: Antifungal agents

Exert fungicidal effect by altering permeability of fungal cell membrane. Mechanism of action also may involve an alteration of RNA and DNA metabolism or an intracellular accumulation of peroxide toxic to the fungal cell.

Drug NameNystatin (Mycostatin)
DescriptionFungicidal and fungistatic antibiotic obtained from Streptomyces noursei. Effective against various yeasts and yeastlike fungi. Changes permeability of fungal cell membrane after binding to cell membrane sterols, causing cellular contents to leak.
Treatment should continue until 48 h after disappearance of symptoms.
Adult DoseThrush: (1:100,000 U/mL) 4-6 mL PO swish and swallow qid
Chronic intertrigo: Nystatin in talc, 100,000 U/g (15 g or 30 g) bid; taper as conditions improves; use unscented baby powder adjunctively
Tablets: Insert 1 tab intravaginally qhs for 14 d
adjunctively
Pediatric DoseInfants: 1 mL to gums and either side of mouth qid; few gtt ingested as part of treatment
Preterm infants: 0.5 mL to either side of mouth qid
Treat for 10-14 d or until 48-72 h after resolution of symptoms
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsVirtually no adverse effects when used topically; may cause GI tract distress or diarrhea if taken in large doses PO; do not use to treat systemic mycoses

Drug NameMiconazole (Micatin, Monistat-Derm, Monistat)
DescriptionDamages fungal cell wall membrane by inhibiting biosynthesis of ergosterol. Membrane permeability is increased causing nutrients to leak out, resulting in fungal-cell death.
Lotion is preferred in intertriginous areas. If cream is used, apply sparingly to avoid maceration effects.
Adult DoseTablets: Insert 1 suppository intravaginally qhs for 7 d (100 mg) or 3 d (200 mg)
Intravaginal cream: Insert 1 applicator intravaginally qhs for 7 d
Topical: Apply 2% cream/powder/spray to affected areas bid for 7 d
Pediatric DoseTopical: Apply 2% cream/powder/spray to affected areas bid for 7 d
ContraindicationsDocumented hypersensitivity; first trimester of pregnancy
InteractionsNone reported
PregnancyC - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
PrecautionsDiscontinue if sensitivity or chemical irritation occurs; for external use only; avoid contact with eyes; local reactions to 0.5-1.5% concentrations include dyspareunia, mild vaginal or vulvar erythema, burning, pruritus, urticaria, and rash

Drug NameClotrimazole (Lotrimin, Mycelex, Gyne-Lotrimin)
DescriptionBroad-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 DoseThrush: 10 mg troche dissolved 5 times/d for 14 d
Tablets: 100 mg: Insert 1 tab intravaginally qhs for 7 d
500 mg: Insert 1 tab intravaginally hs once
Intravaginal cream: Insert 1 applicator qhs for 7 d
Topical: Apply 1% cream, solution, or lotion to affected areas bid for 7 d
Pediatric DoseTopical: Apply 1% cream, solution, or lotion to affected areas bid for 7 d
ContraindicationsDocumented hypersensitivity; first trimester of pregnancy
InteractionsNone reported
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsFor external use only; avoid contact with eyes; discontinue if irritation or sensitivity develops; local reactions to 0.5-1.5% concentrations include dyspareunia, mild vaginal or vulvar erythema, burning, pruritus, urticaria, and rash

Drug NameFluconazole (Diflucan)
DescriptionSynthetic oral antifungal (broad-spectrum bistriazole) that selectively inhibits fungal cytochrome P-450 and sterol C-14 alpha-demethylation.
Adult DoseThrush (non-AIDS related): 200 mg PO single dose or 100 mg/d for 5 d
Thrush (AIDS related): 200 mg PO first day, then 100 mg qd until improvement (3-4 d)
Continued suppressive treatment: 100 mg PO qwk
Intertrigo: 100 mg PO qd for 7-14 d
Vaginal: 150 mg PO single dose
Pediatric Dose3-6 mg/kg PO qd for 14-28 d or 6-12 mg/kg qd depending on severity of infection
ContraindicationsDocumented hypersensitivity
InteractionsLevels may increase with hydrochlorothiazides; fluconazole levels may decrease with chronic 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 fluconazole coadministration; increases in cyclosporine concentrations may occur when administered concurrently
PregnancyC - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
PrecautionsAdverse effects include nausea, headache, skin rash, abdominal pain, vomiting, and diarrhea (16% overall rate of adverse effects); rare adverse effects include severe hepatotoxicity, exfoliative dermatitis, and anaphylaxis; monitor closely if rashes develop and discontinue if lesions progress; may cause clinical hepatitis, cholestasis, and fulminant hepatic failure (including death) with underlying medical conditions such as AIDS or malignancy and while taking multiple concomitant medications; not recommended in breastfeeding

Drug NameItraconazole (Sporanox)
DescriptionSynthetic 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 DoseParonychia: 200 mg PO bid for first wk of month for 3 mo
Intertrigo: 100 mg PO qd for 1-2 wk
Pediatric DoseNot established; suggested dose of 100 mg/d PO for systemic fungal infections
ContraindicationsDocumented hypersensitivity; astemizole, oral triazolam, oral midazolam, and cisapride coadministration (results in increased serum levels that may lead to life-threatening arrhythmias)
InteractionsAntacids may reduce absorption of itraconazole; 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 (lovastatin or 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 itraconazole levels (phenytoin metabolism may be altered)
PregnancyC - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
PrecautionsCaution in hepatic insufficiency; rare adverse effects include hepatitis, hypokalemia, hypertension, impotence, and allergic skin reactions

Drug NameTerbinafine (Lamisil)
DescriptionFor treatment of paronychia; allylamine antifungal, which inhibits squalene epoxidase and decreases ergosterol synthesis, causing fungal-cell death.
Use medication until symptoms significantly improve.
Duration of treatment should be > 1 wk but not > 4 wk. May not be as effective for candidal infections as azole antifungals.
Adult DoseParonychia: 250 mg PO qd for 12 wk
Pulse dosing: 500 mg PO qd for first wk of month for 2 mo (fingernails) or 4 mo (toenails)
Pediatric DoseWeight-based dosing (PO):
12-20 kg: 62.5 mg/d
20-40 kg: 125 mg/d
>40 kg: 250 mg/d
Treatment duration as in adults
ContraindicationsDocumented hypersensitivity
InteractionsMay decrease cyclosporine effects; toxicity of terbinafine may increase with rifampin and cimetidine
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsRare cases of symptomatic cholestatic hepatitis have been reported; discontinue if chemical irritation or signs of hepatobiliary dysfunction develop; joint and muscle pains, rash, and decreased WBC count can occur



Patient Education



Medical/Legal Pitfalls

  • Duong et al15 noted 2 cases of extensive cutaneous candidiasis complicating cutaneous T-cell lymphoma. Be aware that cutaneous T-cell lymphoma may underlie extensive candidiasis.



The authors and editors of eMedicine gratefully acknowledge the contributions of previous author, Thomas Vaughan, MD, to the development and writing of this article.



Media file 1:  A moist, erosive, pruritic patch of the perianal skin and perineum (with satellite pustule formation) is demonstrated in this woman with extensive candidosis.
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Media file 2:  Discrete superficial pustules developed within hours of birth on the hand of an otherwise healthy newborn. A potassium hydroxide preparation revealed spores and pseudomycelium, and culture demonstrated the presence of Candida albicans.
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Media file 3:  Dry, red, superficially scaly, pruritic macules and patches on the penis represent candidal balanitis.
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Media file 4:  White plaques are present on the buccal mucosa and the undersurface of the tongue and represent thrush. When wiped off, the plaques leave red erosive areas.
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Media file 5:  Erythema, maceration, and satellite pustules in the axilla, accompanied by soreness and pruritus result in a form of intertrigo.
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Media file 6:  A nailfold with candidal infection becomes erythematous, swollen, and tender with an occasional discharge
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Media file 7:  Soreness and cracks at the lateral angles of the mouth (angular cheilitis) is a frequent expression of candidosis in elderly individuals.
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Media file 8:  Fine superficial pustules on an erythematous patchy base are suggestive of candidosis.
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Media file 9:  Candida infection should be in the differential diagnosis when one or more nails become discolored, has subungual discoloration, nailplate separation from the nailbed, and lack evidence of a dermatophyte.
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Media file 10:  Candidiasis. Courtesy of Hon Pak, MD.
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  1. Foureur N, Vanzo B, Meaume S, Senet P. Prospective aetiological study of diaper dermatitis in the elderly. Br J Dermatol. Nov 2006;155(5):941-6. [Medline].
  2. Kränke B, Trummer M, Brabek E, Komericki P, Turek TD, Aberer W. Etiologic and causative factors in perianal dermatitis: results of a prospective study in 126 patients. Wien Klin Wochenschr. Mar 2006;118(3-4):90-4. [Medline].
  3. Nardin ME, Pelegri DG, Manias VG, Mendez Ede L. [Etiological agents of dermatomycoses isolated in a hospital of Santa Fe City, Argentina]. Rev Argent Microbiol. Jan-Mar 2006;38(1):25-7. [Medline].
  4. Nishimoto K. [An epidemiological survey of dermatomycoses in Japan, 2002]. Nippon Ishinkin Gakkai Zasshi. 2006;47(2):103-11. [Medline].
  5. Ramirez De Knott HM, McCormick TS, Do SO, Goodman W, Ghannoum MA, Cooper KD, et al. Cutaneous hypersensitivity to Candida albicans in idiopathic vulvodynia. Contact Dermatitis. Oct 2005;53(4):214-8. [Medline].
  6. Gibney MD, Siegfried EC. Cutaneous congenital candidiasis: a case report. Pediatr Dermatol. Dec 1995;12(4):359-63. [Medline].
  7. Raval DS, Barton LL, Hansen RC, Kling PJ. Congenital cutaneous candidiasis: case report and review. Pediatr Dermatol. Dec 1995;12(4):355-8. [Medline].
  8. Nico MM, Rivitti EA. 'Decubital candidosis': a study of 26 cases. J Eur Acad Dermatol Venereol. May 2005;19(3):296-300. [Medline].
  9. Yanagisawa N, Suganuma A, Takeshita N, Imamura A, Ajisawa A, Negishi M, et al. A case of disseminated candidiasis as an initial presentation of AIDS. Kansenshogaku Zasshi. Jul 2007;81(4):459-62. [Medline].
  10. Andrews JI, Fleener DK, Messer SA, Hansen WF, Pfaller MA, Diekema DJ. The yeast connection: is Candida linked to breastfeeding associated pain?. Am J Obstet Gynecol. Oct 2007;197(4):424.e1-4. [Medline].
  11. Agarwal S, Sharma M, Mehndirata V. Solitary ecthyma gangrenosum (EG)-like lesion consequent to Candida albicans in a neonate. Indian J Pediatr. Jun 2007;74(6):582-4. [Medline].
  12. Xi L, Li X, Zhang J, Lu C, Xie T, Yin R. Good response in a patient with deep-seated subcutaneous ulcer due to Candida species. Mycopathologia. Aug 2007;164(2):77-80. [Medline].
  13. Diana A, Epiney M, Ecoffey M, Pfister RE. "White dots on the placenta and red dots on the baby": congential cutaneous candidiasis--a rare disease of the neonate. Acta Paediatr. Jul 2004;93(7):996-9. [Medline].
  14. Sundaram SV, Srinivas CR, Thirumurthy M. Candidal intertrigo: treatment with filter paper soaked in Castellani's paint. Indian J Dermatol Venereol Leprol. Sep-Oct 2006;72(5):386-7. [Medline].
  15. Duong T, Ingen-Housz-Oro S, Gaulier A, Petit A, Dubertret L, Sigal-Grinberg M. [Extensive cutaneous candidiasis revealing cutaneous T-cell lymphoma: 2 cases]. Ann Dermatol Venereol. Jun-Jul 2006;133(6-7):566-70. [Medline].
  16. Aly R, Berger T. Common superficial fungal infections in patients with AIDS. Clin Infect Dis. May 1996;22 Suppl 2:S128-32. [Medline].
  17. Aridogan IA, Ilkit M, Izol V, Ates A. Malassezia and Candida colonisation on glans penis of circumcised men. Mycoses. Sep 2005;48(5):352-6. [Medline].
  18. Elewski BE. Cutaneous mycoses in children. Br J Dermatol. Jun 1996;134 Suppl 46:7-11: discussion 37-8. [Medline].
  19. Fotos PG, Lilly JP. Clinical management of oral and perioral candidosis. Dermatol Clin. Apr 1996;14(2):273-80. [Medline].
  20. Gilbert DN, Moellering RC, Merle AS. Sanford Guide to Antimicrobial Therapy. 35th ed. 2005.
  21. Hay RJ. Yeast infections. Dermatol Clin. Jan 1996;14(1):113-24. [Medline].
  22. Hedderwick S, Kauffman CA. Opportunistic fungal infections: superficial and systemic candidiasis. Geriatrics. Oct 1997;52(10):50-4, 59. [Medline].
  23. Hoppe JE. Treatment of oropharyngeal candidiasis and candidal diaper dermatitis in neonates and infants: review and reappraisal. Pediatr Infect Dis J. Sep 1997;16(9):885-94. [Medline].
  24. Marquart KH. Electron microscopy reveals fungal cells within tumor tissue from two African patients with AIDS-associated Kaposi sarcoma. Ultrastruct Pathol. May-Jun 2006;30(3):187-92. [Medline].
  25. Rang HP, Dale MM, et al. Pharmacology. 689-90. New York, NY: Churchill Livingstone; 1995:756-60.
  26. Seebacher C, Abeck D, Brasch J, Effendy I, Ginter-Hanselmayer G, Haake N, et al. [Candidiasis of the skin]. J Dtsch Dermatol Ges. Jul 2006;4(7):591-6. [Medline].
  27. Smolinski KN, Shah SS, Honig PJ, Yan AC. Neonatal cutaneous fungal infections. Curr Opin Pediatr. Aug 2005;17(4):486-93. [Medline].
  28. Takechi M. Minimum effective dosage in the treatment of chronic atopic dermatitis with itraconazole. J Int Med Res. May-Jun 2005;33(3):273-83. [Medline].
  29. Wang SM, Yang YJ, Chen JS, Lin HC, Chi CY, Liu CC. Invasive fungal infections in pediatric patients with leukemia: emphasis on pulmonary and dermatological manifestations. Acta Paediatr Taiwan. May-Jun 2005;46(3):149-55. [Medline].
  30. Warren NG. Taxonomy and introduction. Dermatol Clin. Jan 1996;14(1):1-7. [Medline].

Candidiasis, Cutaneous excerpt

Article Last Updated: Mar 26, 2008