Granulomatosis with polyangiitis (breast manifestations)
Citation, DOI, disclosures and article data
At the time the article was created Avni K P Skandhan had no recorded disclosures.View Avni K P Skandhan's current disclosures
At the time the article was last revised Daniel J Bell had no recorded disclosures.View Daniel J Bell's current disclosures
Breast involvement in granulomatosis with polyangiitis is seen in patients with avid systemic manifestations.
Clinically they can mimic carcinoma as a palpable, tender mass.
Granulomatosis with polyangiitis (or formerly known as Wegeners granulomatosis) is a necrotizing granulomatous vasculitis which is characterized by necrotizing granulomatous inflammation, small and medium-sized vessel vasculitis, and focal necrotizing glomerulonephritis.
The commonest areas of involvement are the respiratory tracts and kidneys, but the disease can affect any organ system.
May be seen as an irregular and high-density mass.
Treatment and prognosis
The treatment for granulomatosis with polyangiitis depends on the severity of the disease. Severe disease can be treated with corticosteroids and cyclophosphamide. For less severe disease, the treatment may be corticosteroids and methotrexate. Approximately half of patients with granulomatosis with polyangiitis may experience a relapse within 2 years of stopping treatment.
- 1. Neralić-Meniga I, Ivanovi-Herceg Z, Mazuranić I et-al. Wegener's granulomatosis of the breast. Wien. Klin. Wochenschr. 2006;118 (3-4): 120-3. doi:10.1007/s00508-006-0536-y - Pubmed citation
- 2. Pambakian H, Tighe JR. Breast involvement in Wegener's granulomatosis. J. Clin. Pathol. 1971;24 (4): 343-7. Free text at pubmed - Pubmed citation