T. Kitahara et al., CASE OF PROPYLTHIOURACIL-INDUCED VASCULITIS ASSOCIATED WITH ANTINEUTROPHIL CYTOPLASMIC ANTIBODY (ANCA) - REVIEW OF LITERATURE, Clinical nephrology, 47(5), 1997, pp. 336-340
A 39-year-old Japanese woman had been receiving propylthiouracil for 5
years for hyperthyroidism when she developed myalgia, scleritis, prot
einuria, fever, and inflammation of the nose. Examination of a renal b
iopsy specimen showed focal segmental necrotizing glomerulonephritis.
Indirect immunofluorescent staining showed a highly positive perinucle
ar pattern of anti-neutrophil cytoplasmic antibody (ANCA) in her serum
. Enzyme-linked immunosorbent assay (ELISA) of the ANCA showed positiv
ity for anti-proteinase 3, anti-myeloperoxidase, anti-leukocyte elasta
se, and anti-lactoferrin, but anti-cathepsin G and anti-lysozyme were
negative. Because ELISA showed the titer of anti-leukocyte elastase an
tibody to be markedly elevated, we challenged this data by performing
dot blot analysis. The patient's serum reacted with the native form, b
ut not with denatured leukocyte elastase. Propylthiouracil-induced vas
culitis was suspected. Symptoms abated within 2 weeks and all values o
f ANCA were reduced after the drug was withdrawn. Vasculitis is a rare
side-effect of propylthiouracil therapy. Recently it was reported in
association with ANCA. We present the findings of this patient and com
pare them with those described in 19 published cases of propylthiourac
il-induced vasculitis associated with ANCA.