Journal List > Tuberc Respir Dis > v.70(3) > 1001601

Jeong, Kang, Park, Kim, Kim, Kim, and Song: A Case of Pulmonary Fibrosis with Microscopic Polyangiitis

Abstract

A 65-year-old woman was admitted due to poor oral intake and a dry cough over the previous 3 months. The physical examination was remarkable for bibasilar crackles, and plain chest radiography showed reticulation in both lower lung fields. A pulmonary function test demonstrated a restrictive pattern with a reduced diffusing capacity of the lung for carbon monoxide. High resolution computed tomography showed reticulation and honey-combing in both peripheral lung zones, which was consistent with usual interstitial pneumonia pattern. Her skin showed livedo reticularis. The erythrocyte sedimentation rate and C-reactive protein level were elevated, and hematuria was noted on urinary analysis. A serologic test for auto-antibodies showed seropositivity for Myeloperoxidase-Anti-neutrophil cytoplasmic antibody (MPO-ANCA). A kidney biopsy was performed and showed focal segmental glomerulosclerosis. She was diagnosed as having pulmonary fibrosis with microscopic polyangiitis (MPA) and treated with high dose steroids. Here we report a case of pulmonary fibrosis coexistent with microscopic polyangiitis.

Figures and Tables

Figure 1
Chest PA shows coarse reticular opacities in both peripheral lung zone.
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Figure 2
High-resolution CT shows reticular opacity and honey-combing in both peripheral lung zone. CT: computer tomography.
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Figure 3
Medium sized vessel wall shows fibrinoid necrosis (H&E, ×200).
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Figure 4
Glomerulus shows focal fibrinoidnecrosis and interstitial inflammatory cell infiltration are observed (H&E, ×200).
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