Prague Med. Rep. 2017, 118, 95-99

https://doi.org/10.14712/23362936.2017.9

IgG4-related Disease – A Patient with Multiple Organ Involvement

Miroslav Průcha, Lenka Sedláčková

Department of Clinical Biochemistry, Haematology and Immunology, Na Homolce Hospital, Prague, Czech Republic

Received March 27, 2017
Accepted August 28, 2017

References

1. Brito-Zerón, P., Ramos-Casals, M., Bosch, X., Stone, J. H. (2014) The clinical spectrum of IgG4-related disease. Autoimmun. Rev. 13, 1203–1210. <https://doi.org/10.1016/j.autrev.2014.08.013>
2. Ebbo, M., Grados, A., Bernit, E., Vely, F., Boucraut, J., Harle, J. R., Daniel, L., Schleinitz, N. (2012) Pathologies associated with serum IgG4 elevation. Int. J. Rheumatol. 2012, 602809. <https://doi.org/10.1155/2012/602809> <PubMed>
3. Kamisawa, 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>
4. Mahajan, V. S., Mattoo, H., Deshpande, V., Pillai, S. S., Stone, J. H. (2014) IgG4-related disease. Annu. Rev. Pathol. 9, 315–347. <https://doi.org/10.1146/annurev-pathol-012513-104708>
5. Průcha, 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(1), 34–41. <https://doi.org/10.14712/23362936.2016.3>
6. Stone, 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>
7. Van Bommel, E. F. H., Siemes, C., Hak, L. E., van der Veer, S. J., Hendriksz, T. T. (2007) Long-term renal and patient outcome in idiopathic retroperitoneal fibrosis treated with prednisone. Am. J. Kidney Dis. 49, 615–625. <https://doi.org/10.1053/j.ajkd.2007.02.268>
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ISSN 1214-6994 (Print) ISSN 2336-2936 (Online)

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