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Basics ⬇

Basics

Overview

  • Lymphomatoid granulomatosis is a rare lymphoproliferative disorder predominantly involving the lungs.
  • Rare pulmonary disease of dogs and cats characterized by angiocentric and angiodestructive proliferation and infiltration by atypical lymphoid cells.

Signalment

  • Dog and cat
  • Median age-5.75 years (range, 1.5–14 years) in dogs
  • No breed predilection but more common in large breeds and pure breeds
  • No gender predisposition

Signs

  • Progressive respiratory signs including cough and dyspnea
  • Serous nasal discharge
  • Exercise intolerance
  • Weight loss
  • Anorexia
  • Fever in 50% of patients
  • Duration- days to weeks

Causes & Risk Factors

Unknown

Diagnosis ⬆ ⬇

Diagnosis

Differential Diagnosis

  • Mycotic, bacterial, or aspiration pneumonia
  • Primary or metastatic pulmonary neoplasia
  • Atypical pulmonary lymphoma

CBC/Biochemistry/Urinalysis

  • No consistent abnormalities
  • Neutrophilic leukocytosis, eosinophilia, and basophilia may be common

Other Laboratory Tests

Some dogs have concurrent heartworm disease and/or test positive for heartworms.

Imaging

  • Radiography-reveals lobar pulmonary consolidation (e.g., mass lesions), hilar lymphadenomegaly, and pleural effusion.
  • Lesions-unilateral or bilateral.

Diagnostic Procedures

  • Biopsy-for definitive diagnosis (adequate tissue sample size required for accurate diagnosis).
  • Immunohistochemistry is required on the biopsied tissue (CD3, CD20, CD79).

Pathologic Findings

  • Gross-multiple pulmonary nodules with a predilection for the caudal lung lobes with metastasis or involvement of hilar lymph nodes.
  • Histologic-characterized by sheets of atypical lymphoid and plasmacytoid cells admixed with fewer eosinophils and small lymphocytes in the pulmonary blood vessels. The lymphocytes can be of B-cell and T-cell lineage, with Reed-Sternberg-like cells reported.
  • Cytologic-may appear as sterile eosinophilic and neutrophilic inflammation with reactive macrophages.
  • Systemic spread is possible-to liver, heart, kidneys, spleen, pancreas, adrenal gland, and other organs.

Treatment ⬆ ⬇

Treatment

Medications ⬆ ⬇

Medications

Drug(s)

Combination protocol-CHOP or other combination protocol suitable for lymphoma. No standard treatment protocol has been systemically evaluated.

Contraindications/Possible Interactions

  • Myelosuppression-caused by cytotoxic drugs
  • Hemorrhagic cystitis-caused by cyclophosphamide

Follow-Up ⬆ ⬇

Follow-Up

Patient Monitoring

Same as for lymphoma treated by chemotherapy

Possible Complications

  • Dyspnea as disease progresses
  • Depression
  • Anorexia
  • Myelosuppression caused by chemotherapy

Expected Course and Prognosis

Median survival in dogs with systemic chemotherapy has been reported to be approximately 12 months; however, range for survival may be broad based upon initial response to therapy. The reported survival is compounded by the difficulty of accurately diagnosing the disease.

Miscellaneous ⬆

Miscellaneous

Associated Conditions

No known definitive associations

Synonyms

  • Eosinophilic pulmonary granulomatosis
  • Granulomatosis
  • Lymphoid granulomatosis
  • Lymphoproliferative angiitis

Abbreviation

CHOP = cyclophosphamide, hydroxydaunorubicin (doxorubicin), vincristine (Oncovin), and prednisone

Suggested Reading

Berry CR, Moore PF, Thomas WP, et al. Pulmonary lymphomatoid granulomatosis in seven dogs (1976–1987). J Vet Intern Med 1990, 4:157–166.

Bounous DI, Bienzle D, Miller-Liebl D. Pleural effusion in a dog. Vet Clin Path 2000, 29:55–58.

Hatoya S, Kumagai D, Takeda S, et al. Successful management with CHOP for pulmonary lymphomatoid granulomatosis in a dog. J Vet Med Sci 2011, 73(4):527–530.

Park HM, Hwang DN, Kang BT, et al. Pulmonary lymphomatoid granulomatosis in a dog: Evidence of immunophenotypic diversity and relationship to human pulmonary lymphomatoid granulomatosis and pulmonary Hodgkin's disease. Vet Pathol 2007, 44:921–923.

Author Nick Dervisis

Consulting Editor Timothy M. Fan

Acknowledgment The authors and editors acknowledge the prior contribution of Wallace B. Morrison.