Journal List > J Rheum Dis > v.21(4) > 1064126

Kim, Huh, Cheon, Cho, Ko, Kim, Kim, Choi, and Lee: A Case of Antineutrophil Cytoplasmic Antibody-negative Granulomatosis with Polyangiitis Presenting as Breast Mass

Abstract

Granulomatosis with polyangiitis (GPA) is a disease characterized by a granulomatous necrotizing vasculitis of the small vessels, along with the presence of antineutrophil cytoplasmic antibody (ANCA), serologically. GPA is a multisystem disease, in which the diagnosis is frequently based on respiratory and renal manifestations, with rare breast invasion. To date, several cases of breast invasion by GPA have been published, and most cases have been positive for ANCA. However, ANCA-negative forms of breast invasion by GPA are extremely rare and have not been reported in Korea thus far. Therefore, we report a case of ANCA-negative GPA in a 70-year-old woman, who was initially presented with a localized palpable mass in the left breast.

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Figure 1.
(A) Breast ultrasonography shows the lesion which is the prominent superficial vessels with diffuse wall thickening (arrows) and increased echogenicity of subcutaneous fat, surrounding them (arrow heads). (B) Follow-up breast ultrasonography after treatment shows the lesion is replaced by normal vessel conditions and does not obtain increased echogenicity of subcutaneous fat anymore.
jrd-21-219f1.tif
Figure 2.
Histopathologic specimen of the breast demonstrates granulomatous inflammation in the small artery, media (arrow) and fibrinoid necrosis with neutrophilic infiltration in small artery, intima (arrow heads) (Hematoxylin and eosin, original magnification ×200).
jrd-21-219f2.tif
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