A case report of granulomatous polyangiitis complicated by tuberculous lymphadenitis
Iijima Y, Kobayashi Y, Uchida Y, Tsutsui T, Kakizaki Y, Naganuma T, Tsukamoto K, Oyama T, et al. (9 authors)
Medicine · 2018-10
Abstract
Rational Granulomatous polyangiitis (GPA) is a type of vasculitis involving medium and small arteries, typically affecting the upper and lower respiratory tract with coexisting glomerulonephritis. GPA is also characterized by necrotizing granulomatous inflammation and the presence of antineutrophil cytoplasm antibodies (ANCA). So far, various infections have lead to elevation of titers of serum ANCA, making it difficult to diagnose. Patient concerns We report a 50-year-old woman who was diagnosed as tuberculous lymphadenitis. During the treatment by anti-tuberculosis (TB) drugs, rapidly progressive renal failure and pleurisy had appeared with elevated titer of PR3-ANCA. Renal biopsy revealed crescentic glomerulonephritis. Diagnosis Renal biopsy revealed crescentic glomerulonephritis and diagnosis of GPA was made. Interventions Steroid therapy had been started with continuation of anti-TB drugs. Outcomes Renal dysfunction had gradually recovered and pleurisy had disappeared with decreasing titer of PR3-ANCA. Lessons This is the first report of GPA complicated by TB infection. When we encounter a case with rapidly progressive renal failure during the TB infection, complication of GPA should be suspected as 1 of the different diagnosis.
MeSH terms
- Humans
- Mycobacterium tuberculosis
- Tuberculosis, Lymph Node
- Antibodies, Antineutrophil Cytoplasmic
- Antibodies, Bacterial
- Diagnosis, Differential
- Tomography, X-Ray Computed
- Biopsy
- Middle Aged
- Female
- Granulomatosis with Polyangiitis