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Basics

Basics

Overview

  • Considered to be a benign variant of systemic lupus erythematosus.
  • One of the most common immune-mediated skin diseases in dogs.
  • Predominantly involves the nasal planum, face, and ears with rare lesions beyond the head.

Signalment

  • Dogs and cats.
  • Very uncommon in cats.
  • Predominant breeds-collie, German shepherd dog, Siberian husky, Shetland sheepdog, Alaskan malamute, chow chow, and their crosses.
  • No age predilection.

Signs

  • Initial symptom: depigmentation of nasal planum and/or lips.
  • Depigmentation progresses to erosions and ulcerations.
  • Loss of normal “cobblestone” architecture of the nasal planum.
  • Tissue loss and scarring can occur.
  • Chronic lesions are fragile and may easily hemorrhage; rarely severe hemorrhage from arteriole damage.
  • May also involve pinnae and periocular region; rarely feet and genitalia.

Causes & Risk Factors

  • Exact mechanism undetermined; actinic radiation may alter antigenic nature of keratinocytes.
  • Seasonal and geographic exacerbation-associated with increased actinic radiation.

Diagnosis

Diagnosis

Differential Diagnosis

Major Considerations

  • Other immune-mediated diseases (PF, PE, SLE)
  • Drug reaction
  • Dermatomyositis
  • Nasal dermatophytosis
  • Mucocutaneous pyoderma
  • Insect bite hypersensitivity

Other (Rare) Considerations

  • Contact allergy
  • Zinc-responsive dermatosis
  • Trauma
  • Superficial necrolytic dermatitis
  • Epitheliotropic cutaneous T-cell lymphoma
  • Squamous cell carcinoma

CBC/Biochemistry/Urinalysis

Normal unless due to an underlying cause

Other Laboratory Tests

ANA, LE preparation, and Coombs' tests-usually normal or negative except in SLE.

Other Diagnostic Procedures

  • Biopsy and histopathology will differentiate DLE from other disorders.
  • Biopsies of early lesions: depigmented areas, mild erosions, or mildly crusted lesions are preferable for diagnosis.

Pathologic Findings

  • Histopathology is characterized by interface-lichenoid dermatitis with prominent basal cell apoptosis, varying degrees of epidermal atrophy, and pigment incontinence.
  • Not easily differentiated from mucocutaneous pyoderma by histopathology (treatment with antibiotics prior to sampling is helpful).
  • Avoid sampling severely crusted, ulcerative lesions if possible.
  • Immunopathologic examination may be done but is usually not necessary.

Treatment

Treatment

Medications

Medications

Drug(s)

  • Topical therapy:
    • Glucocorticosteroids-initially, a potent fluorinated product (e.g., 0.1% fluocinolone) q24h for 14 days; then q48–72h; once in remission switch to less-potent product (e.g., 0.5% or 2.5% hydrocortisone) if possible.
    • Tacrolimus ointment (0.1%) q12–24h initially then taper to q24–72h once in remission.
  • Systemic therapy:
    • Tetracycline and niacinamide-250 mg each PO q8h for dogs <10 kg; 500 mg PO q8h for larger dogs (alternatives include doxycycline 10 mg/kg PO q24h and minocycline 5 mg/kg PO q12h).
    • Prednisone-consider for severe or non-responsive cases; 2–4 mg/kg/day either solely or in combination with azathioprine 2 mg/kg PO q48h; taper prednisone to 0.5–1 mg/kg PO q48h for long-term maintenance.
    • Cyclosporine-5–10 mg/kg PO q24h as alternative immunosuppressive therapy.
  • Consider systemic antibiotic treatment for a minimum of 3–4 weeks prior to systemic immunosuppressive therapy to differentiate from mucocutaneous pyoderma.
  • Vitamin E 10–20 IU/kg PO q12h; may help reduce inflammation and protect the skin.
  • Hydroxychloroquine-5 mg/kg q24h; antimalarial drug that has been used in human cases.

Follow-Up

Follow-Up

Patient Monitoring

  • Recheck 2–4 weeks after initiating treatment to evaluate for clinical response.
  • CBC and biochemistry-every 12 months if using topical therapy and every 3–6 months if using systemic therapy.
  • CBC and platelet counts-every 2 weeks for the first month; then every 3–6 months while on azathioprine.

Prevention/Avoidance

Affected animals should avoid ultraviolet light exposure.

Possible Complications

  • Scarring
  • Secondary pyoderma
  • Hemorrhage
  • Disfigurement

Expected Course and Prognosis

  • Progressive but not usually life-threatening if left untreated.
  • With proper treatment, expect remission in majority of cases.
  • Cases requiring chronic immunosuppressive therapy have a more guarded prognosis, but remissions are common with more aggressive therapy.

Miscellaneous

Miscellaneous

Synonyms

  • Collie nose
  • Nasal solar dermatitis.

Abbreviations

  • ANA = antinuclear antibody
  • DLE = discoid lupus erythematosus
  • LE = lupus erythematosus
  • PE = pemphigus erythematosus
  • PF = pemphigus foliaceus
  • SLE = systemic lupus erythematosus

Author Dawn E. Logas

Consulting Editor Alexander H. Werner

Acknowledgment The author and editor acknowledge the previous contribution of Wayne Rosenkrantz.

Suggested Reading

Griffies JD, Mendelsohn CL, Rosenkrantz WR, et al. Topical 0.1% tacrolimus for the treatment of discoid lupus erythematosus and pemphigus erythematosus in dogs. J Am Anim Hosp Assoc 2004, 40:2941.

Oberkirchner U, Linder KE, Thierry O. Successful treatment of a novel generalized variant of canine discoid lupus erythematosus with oral hydroxychloroquine. Vet Dermatol 2011, 24:65e16.

Rosenkrantz WS. Discoid lupus erythematosus. In: Current Veterinary Dermatology. St. Louis, MO: Mosby, 1993.

Wiemelt SP, Goldschmidt MH, Greek JS, et al. A retrospective study comparing the histopathological features and response to treatment in two canine nasal dermatoses, DLE and MCP. Vet Dermatol 2004, 15:341348.