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Basics

Basics

Overview

  • Protozoan-genus Leishmania; causes two types of disease: cutaneous: and visceral.
  • Affected dogs in the United States invariably acquired infection in another country unless part of the endemic foxhound population.
  • L. donovani infantum-Mediterranean basin, Portugal, and Spain; sporadic cases in Switzerland, northern France, and the Netherlands.
  • L. donovani complex or L. braziliensis-endemic areas of South and Central America and southern Mexico.
  • Considered endemic in foxhounds in the United States.
  • Sandfly vectors-transmit flagellated parasites into the skin of a host. Vector unknown in United States.
  • Cats-often localizes in skin.
  • Dogs-invariably develop visceral disease; renal failure is the most common cause of death.
  • Incubation period-1 month to several years.

Signalment

  • Dogs-virtually all develop visceral (systemic), disease; 90% also have cutaneous involvement; no sex or breed predilection.
  • Cats-cutaneous disease (rare); no sex or breed predilection.

Signs

Visceral

  • Exercise intolerance; weight loss, anorexia, diarrhea, vomiting, epistaxis, and melena; lymphadenopathy and cutaneous lesions (90% of cases); emaciation; signs of renal failure (polyuria, polydipsia, vomiting) possible; neuralgia, polyarthritis, polymyositis, osteolytic lesions, and proliferative periostitis rare; fever and splenomegaly (30%); death is usually due to chronic proteinuric nephritis progressing to end-stage kidney disease, nephrotic syndrome, and/or systemic hypertension.

Cutaneous

  • Dogs-hyperkeratosis is the most prominent finding; excessive epidermal scale with thickening, depigmentation, and chapping of the muzzle and footpads; hair coat dry, brittle, hair loss, intradermal nodules and ulcers; abnormally long or brittle nails in some patients.
  • Cats-cutaneous nodules (especially on the ears) usually develop.

Causes & Risk Factors

  • Travel to endemic regions (usually the Mediterranean), where dogs are exposed to infected sandflies.
  • Transmission by blood transfusion, in utero, and direct contact can occur.

Diagnosis

Diagnosis

Differential Diagnosis

  • Visceral-blastomycosis; histoplasmosis; systemic lupus erythematosus; metastatic neoplasia; distemper; vasculitis.
  • Cutaneous-other causes of hyperkeratosis.
  • Skin biopsy-hyperkeratotic and nodular lesions; existence of organisms confirms diagnosis.
  • Hyperglobulinemia-differentiate from chronic ehrlichiosis and multiple myeloma.

CBC/Biochemistry/Urinalysis

  • Hyperproteinemia with hyperglobulinemia-nearly 100% of cases.
  • Hypoalbuminemia-95% of cases.
  • Proteinuria-85% of cases.
  • High liver enzyme activity-55% of cases.
  • Thrombocytopenia-50% of cases.
  • Azotemia-up to 45% of cases.
  • Leukopenia with lymphopenia-20% of cases.

Other Laboratory Tests

  • Serologic diagnosis by IFA or ELISA available-most tests give cross-reaction to Trypanosoma cruzi; differentiate based on clinical signs, history, and likelihood of exposure. Rapid in-house immunochromatographic tests are also available.
  • PCR-particularly sensitive on bone marrow, lymph nodes, spleen and skin, but also used to assess blood, bodily fluids, conjunctival scrapings, and histopathologic specimens.

Diagnostic Procedures

  • Cultures-skin, spleen, bone marrow, or lymph node biopsies or aspirates; by the Centers for Disease Control and Prevention.
  • Cytology and histopathology with immunohistopahtology-identify intracellular organisms in biopsies or aspirate specimens (listed above).

Pathologic Findings

  • Cell infiltration (mainly histiocytes and macrophages) and characteristic intracellular amastigote forms especially in skin, lymph nodes, liver, spleen, and kidney.
  • Mucosal ulcerations-stomach, intestine, and colon occasionally found.

Treatment

Treatment

Medications

Medications

Drug(s) Of Choice

  • Sodium stibogluconate and meglumine antimonite may only be available from the CDC.
  • Allopurinol-produces clinical cures but relapses occur. Best when used in combination with other drugs (meglumine or amphotericin B) as maintenance. Dose: 7 mg/kg PO q8h for 3 months, or 10 mg/kg/day PO for 2–24 months.
  • Amphotericin B-0.5–0.8 mg/kg diluted in 50 mL dextrose 5% in water given IV over 1 minute q48h for total dose of 8–15 mg/kg.

Contraindications/Possible Interactions

  • Seriously ill dogs-start antimonial drugs at lower doses.
  • Renal insufficiency-treat before giving antimonial drugs; prognosis depends on renal function at the onset of treatment.
  • Amphotericin B-nephrotoxicity can occur.

Follow-Up

Follow-Up

Miscellaneous

Miscellaneous

Zoonotic Potential

  • Leishmaniasis is a notifiable disease reportable to the CDC.
  • Advise owner of zoonotic potential.

Abbreviations

  • ELISA = enzyme-linked immunosorbent assay
  • IFA = immunofluorescent antibody test
  • PCR = polymerase chain reaction

Suggested Reading

Baneth G, Solano-Gallego L. Leishmaniasis. In: Greene CE, ed., Infectious Diseases of the Dog and Cat, 4rd ed. St. Louis, MO: Saunders Elsevier, 2012, pp. 734749.

Petersen CA, Barr SC. Canine leishmaniasis in North America: emerging or newly recognized? Vet Clin North Am Small Anim Pract 2009, 39:10601074.

Author Stephen C. Barr

Consulting Editor Stephen C. Barr