Prague Med. Rep. 2016, 117, 124-128
https://doi.org/10.14712/23362936.2016.13
IgG4-related Diseases – A Rare Polycystic Form of Ormond’s Disease
References
1. , I., Hendriksz, T. R., Van Bommel, E. F. (2010) Pseudocyst formation in retroperitoneal fibrosis relapse. Br. J. Radiol. 83, e111–e113.
<https://doi.org/10.1259/bjr/81915147>
<PubMed>
2. , T., Zen, Y., Pillai, S., Stone, J. H. (2015) IgG4-related disease. Lancet 385, 1460–1471.
<https://doi.org/10.1016/S0140-6736(14)60720-0>
3. , M., Kolombo, I., Štádler, P. (2016) Combination of steroids and azathioprine in the treatment of Ormond’s disease – a single centre retrospective analysis. Prague Med. Rep. 117, 34–41.
<https://doi.org/10.14712/23362936.2016.3>
4. , P. J. Jr., Feeley, N. (2013) Retroperitoneal fibrosis. Rheum. Dis. Clin. North Am. 39, 365–368.
<https://doi.org/10.1016/j.rdc.2013.02.004>
5. , J. H., Brito-Zerón, P., Bosch, X., Ramos-Casals, M. (2015) Diagnostic approach to the complexity of IgG4-related disease. Mayo Clin. Proc. 90, 927–939.
<https://doi.org/10.1016/j.mayocp.2015.03.020>
