NAVLE Integumentary

Feline Dermatophytosis Study Guide

Dermatophytosis (commonly known as ringworm) is a superficial fungal infection of keratinized structures including skin, hair, and nails in cats. Despite its common name, this condition is not caused by a worm but by fungi called dermatophytes.

Overview and Clinical Importance

Dermatophytosis (commonly known as ringworm) is a superficial fungal infection of keratinized structures including skin, hair, and nails in cats. Despite its common name, this condition is not caused by a worm but by fungi called dermatophytes. This is a high-yield NAVLE topic due to its clinical prevalence, zoonotic potential, and importance in shelter medicine.

Microsporum canis is the causative agent in greater than 90% of feline dermatophytosis cases. The disease is self-limiting in immunocompetent cats (typically resolving within 4 months) but treatment is always recommended to shorten clinical course, reduce environmental contamination, and prevent zoonotic transmission.

High-YieldDermatophytosis affects less than 4% of cats with skin disease - it is NOT the most common feline skin condition despite popular belief. FIV/FeLV status alone does NOT increase risk of dermatophytosis.
Classification Species Clinical Significance
Zoophilic Microsporum canis Greater than 90% of feline cases; cats are natural reservoir; highly zoonotic; fluoresces under Wood's lamp
Zoophilic Trichophyton mentagrophytes Less common; rodent reservoir; does NOT fluoresce
Geophilic Microsporum gypseum Soil reservoir; sporadic infections; does NOT fluoresce

Etiology and Pathogenesis

Causative Organisms

Dermatophytes are keratinophilic fungi that utilize keratin as a nutrient source. They are classified by their natural reservoir:

Pathogenesis

The infection cycle follows these key steps:

  • Exposure: Arthrospores contact skin (direct animal contact or fomite transmission)
  • Adhesion: Spores adhere to keratinocytes within 2 hours of contact
  • Germination: Requires microtrauma/abraded skin for successful invasion
  • Invasion: Hyphae penetrate stratum corneum and hair follicles
  • Shedding: Infected hairs with arthrospores shed into environment (can occur within 7 days)
NAVLE TipM. canis is NOT part of normal feline skin flora - isolation always indicates exposure. However, distinguish between true infection and 'fomite carriage' (mechanical spore carriage without active infection).

Risk Factors and Predispositions

Risk Factor Clinical Details
Breed Predisposition Persian cats significantly over-represented; long-haired breeds more commonly affected; also predisposed to dermatophytic pseudomycetoma
Age Kittens more susceptible due to immature immune system and grooming behavior
Environment Overcrowded conditions (shelters, catteries); warm, humid climates; poor sanitation
Immunosuppression Corticosteroid therapy, cyclosporine, malnutrition, concurrent illness; NOTE: FIV/FeLV status ALONE does not increase risk
Ectoparasites Fleas and Cheyletiella mites create microtrauma facilitating infection

Clinical Presentation

Classic Clinical Signs

Dermatophytosis is a follicular disease, meaning lesions follow hair follicle distribution. Clinical presentation is highly variable - there is no single 'classic' appearance.

Atypical Presentations

  • Asymptomatic carriers: Culture-positive cats with no clinical lesions - especially long-haired breeds
  • Dermatophytic pseudomycetoma: Nodular/subcutaneous lesions almost exclusively in Persian cats
  • Exudative paronychia: Nail bed infection with discharge
  • Kerion: Highly inflammatory, nodular reaction (less common in cats than dogs)

Exam Focus: The 'classic ring' lesion seen in humans is UNCOMMON in cats. Feline lesions are often irregular, asymmetrical patches of alopecia with scaling. Always include dermatophytosis in differentials for any cat with patchy alopecia!

Clinical Finding Description
Alopecia Patchy, irregular, or circular; often multifocal and asymmetrical; broken/stubbled hairs at periphery
Scaling/Crusting Gray, dry, adherent scale; may appear seborrhea-like
Erythema Variable; may be minimal to marked inflammatory response
Papules/Pustules Follicular papules; miliary dermatitis pattern possible
Pruritus Variable - often minimal; may be absent entirely
Distribution Face, pinnae, feet ('hot spot' areas); may be generalized; often asymmetrical

Diagnostic Approach

No single test is the gold standard for diagnosing dermatophytosis. A combination of diagnostic modalities provides the most accurate diagnosis.

Diagnostic Tests Comparison

Wood's Lamp Examination

The Wood's lamp emits long-wave ultraviolet light (320-400 nm, peak 365 nm). M. canis produces a tryptophan metabolite called pteridine that fluoresces a characteristic bright apple-green color.

Technique

  • Allow lamp to warm up for 3-5 minutes before use
  • Examine in a completely dark room
  • Hold lamp 2-4 cm from skin surface
  • Start at head, examine systematically including face, ears, feet, interdigital spaces
  • Gently lift crusts to visualize hairs beneath
  • Look for fluorescence in individual hair shafts, not scales or debris

Interpretation

  • Positive: Bright apple-green fluorescence of hair shafts
  • False positives: Lint, soap, topical medications, doxycycline, lime sulfur residue (yellow/orange/blue)
  • False negatives: 30-50% of M. canis strains; Trichophyton and M. gypseum NEVER fluoresce
High-YieldDuring treatment, as infection resolves, fluorescence moves from the entire hair shaft to just the 'glowing tips' - indicating the proximal (intrafollicular) portion is now clear. Glowing tips may persist for weeks/months after mycological cure!

Direct Microscopic Examination (Trichogram)

Pluck hairs from lesion edges (preferably Wood's lamp positive hairs) and examine microscopically.

Technique

  • Mount hairs in mineral oil or 10-20% KOH (KOH clears keratin debris; incubate overnight)
  • Examine at 10x and 40x magnification
  • Positive findings: Arthrospores (ectothrix pattern) surrounding or within hair shaft; hyphae

Fungal Culture (DTM)

Dermatophyte Test Medium (DTM) is the standard culture medium containing antibiotics (chloramphenicol, cycloheximide) to inhibit bacteria and saprophytic fungi, plus phenol red pH indicator.

Sample Collection

  • Lesional cats: Pluck hairs from lesion periphery; include scales
  • Screening/carriers: MacKenzie toothbrush technique - brush entire coat vigorously with new sterile toothbrush, then press bristles onto DTM

Incubation and Reading

  • Incubate at 25-30°C in dark, humid environment
  • Monitor DAILY for up to 21 days
  • Do not seal lid tightly (allow air exchange)

Interpretation

Positive culture = White/buff/pale yellow FLUFFY colony growth SIMULTANEOUS with red color change (alkaline pH from protein metabolism)

NAVLE TipColor change ALONE is not diagnostic! Must see concurrent white/buff colony growth AND confirm dermatophyte identity by microscopic examination of macroconidia. M. canis macroconidia are spindle-shaped, 6-15 celled, thick-walled with rough surface and terminal knob.
Test Sensitivity Specificity Time Notes
Wood's Lamp 50-70% ~92% Immediate M. canis only
Trichogram Variable High Immediate Requires expertise
DTM Culture High High 7-21 days Gold standard
PCR Greater than 95% ~99% Less than 8 hours Rapid confirmation

Treatment

Treatment requires a three-pronged approach: (1) systemic antifungal therapy, (2) topical therapy, and (3) environmental decontamination.

Systemic Antifungal Therapy

High-YieldItraconazole pulse therapy works because the drug is keratinophilic - it accumulates in hair/skin and persists for up to 4 weeks after discontinuation. NEVER use compounded itraconazole - bioavailability is unreliable!

Monitoring During Systemic Therapy

  • Monitor liver enzymes (ALT) at baseline and periodically - especially with itraconazole
  • If using griseofulvin: CBC every 2 weeks; test for FIV/FeLV before starting
  • Watch for anorexia, vomiting, hepatotoxicity signs

Topical Therapy

Topical therapy is used to disinfect the haircoat and reduce environmental contamination. Whole-body treatment is preferred over spot treatment.

Clipping

Clipping is NOT required for single-cat households. Recommended for multi-cat environments, shelters, or long-haired breeds to reduce environmental contamination and improve topical penetration.

Environmental Decontamination

Critical concept: M. canis arthrospores can survive in the environment for up to 18 months.

  • Effective disinfectants: Dilute bleach (1:10), accelerated hydrogen peroxide, enilconazole
  • Vacuum frequently; dispose of vacuum bags
  • Wash bedding, toys in hot water with bleach
  • Discard items that cannot be effectively cleaned (scratching posts, soft toys)

Treatment Duration and Cure Criteria

Continue treatment until mycological cure is documented - resolution of clinical signs alone is insufficient.

  • Typical treatment duration: 6-12 weeks
  • Cure criteria: Resolution of clinical lesions + negative Wood's lamp (except tips) + TWO consecutive negative fungal cultures 2-4 weeks apart

Prognosis

Excellent in immunocompetent cats with appropriate treatment and environmental management. Recurrence usually indicates inadequate treatment duration, environmental recontamination, or unidentified carrier animals.

Colony Color Media Change Interpretation
White/buff fluffy Red (simultaneous) Suspect dermatophyte - confirm microscopically
Black, green, gray Any Saprophyte/contaminant - NOT dermatophyte
Any Red (delayed) Saprophyte overgrowth - false positive

Zoonotic Considerations

M. canis is highly zoonotic. Approximately 50% of humans exposed to infected cats develop infection.

  • Human presentation: Classic circular, erythematous, scaly 'ring' lesion (tinea corporis)
  • Children, elderly, and immunocompromised individuals at highest risk
  • Advise clients to practice good hygiene, limit direct contact during treatment, seek human medical attention if lesions develop
Drug Dose Protocol Notes
Itraconazole (FIRST LINE) 5 mg/kg PO q24h PULSE: Week 1,3,5 ON; Week 2,4 OFF (3 cycles) Itrafungol licensed for cats; keratinophilic; avoid compounded formulations
Terbinafine 10-30 mg/kg PO q24h Daily or pulse (20 mg/kg for pulse); until cure Give with food; alternative when azoles fail
Griseofulvin 25-50 mg/kg PO q24h Daily with fatty meal; 6-10 weeks CAUTION: Bone marrow suppression; NEVER in FIV+ cats; teratogenic

Memory Aids

"M. CANIS" Mnemonic for Diagnosis

  • M - Most common cause (greater than 90% of feline cases)
  • C - Culture on DTM is gold standard
  • A - Apple-green fluorescence under Wood's lamp
  • N - Not normal flora (isolation = exposure)
  • I - Itraconazole first-line treatment
  • S - Self-limiting but STILL treat!

"PULSE" for Itraconazole Protocol

  • P - Persists in keratin (drug accumulates)
  • U - Use 5 mg/kg daily
  • L - Licensed product only (no compounding)
  • S - Seven days ON, seven days OFF
  • E - Expect 3 cycles (weeks 1, 3, 5)
Agent Protocol Notes
Lime sulfur (1:16) Dip/rinse 2x weekly Gold standard; safe in kittens; yellow staining; odor
Enilconazole (0.2%) Rinse 2x weekly Imaverol; not licensed in all countries
Miconazole/Chlorhexidine shampoo Bath 2x weekly Combined product (2% miconazole + 2% chlorhexidine)

Practice NAVLE Questions

Test your knowledge with 10,000+ exam-style questions, detailed explanations, and timed exams.

Start Your Free Trial →