1. Yang J, Yao LP, Dong MJ, Xu Q, Zhang J, Weng WW, et al. Clinical characteristics and outcomes of propylthiouracil-induced antineutrophil cytoplasmic antibody-associated vasculitis in patients with graves’ disease: a median 38-month retrospective cohort study from a single institution in China. Thyroid. 2017; 27:1469–74.
Article
2. Chen YX, Yu HJ, Ni LY, Zhang W, Xu YW, Ren H, et al. Propylthiouracil-associated antineutrophil cytoplasmic autoantibody-positive vasculitis: retrospective study of 19 cases. J Rheumatol. 2007; 34:2451–6.
3. Tomkins M, Tudor RM, Smith D, Agha A. Propylthiouracilinduced antineutrophil cytoplasmic antibody-associated vasculitis and agranulocytosis in a patient with Graves’ disease. Endocrinol Diabetes Metab Case Rep. 2020; 2020:19–0135.
Article
4. Ortiz-Diaz EO. A 27-year-old woman presenting with refractory hypoxaemic respiratory failure, haemoptysis and thyrotoxicosis: a rare manifestation of propylthiouracil therapy. BMJ Case Rep. 2014; 2014:bcr2014204915.
Article
5. Vicente N, Cardoso L, Barros L, Carrilho F. Antithyroid drug-induced agranulocytosis: state of the art on diagnosis and management. Drugs R D. 2017; 17:91–6.
Article