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

Miroslav Průcha1, Petr Czinner2, Petra Prokopová3

1Department of Clinical Biochemistry, Haematology and Immunology, Na Homolce Hospital, Prague, Czech Republic
2Department of Vascular Surgery, Na Homolce Hospital, Prague, Czech Republic
3Department of Pathology, Na Homolce Hospital, Prague, Czech Republic

Received May 18, 2016
Accepted September 2, 2016

Crossref Cited-by Linking

  • Adam Zden\u011bk, Zeman David, \u010cermák Ale\u0161, Dastych Milan, Doubková Martina, Horváth Theodor, Skorkovská \u0160árka, Adamová Zuzana, \u0158ehák Zden\u011bk, Koukalová Renata, Pour Lud\u011bk, \u0160tork Martin, Krej\u010dí Marta, Sandecká Viera, \u0160ev\u010díková Sabina, Král Zden\u011bk: IgG4-related disease. Clinical manifestation differential diagnosis and recent International Diagnostic Criteria for IgG4-related disease. Vnit\u0159 Lék 2022, 68, E20. <https://doi.org/10.36290/vnl.2022.070>
  • Adam Zden\u011bk, Chovancová Zita, Nová Markéta, Fabian Pavel, \u0158ehák Zden\u011bk, Koukalová Renata, Slávik Marek, Pour Lud\u011bk, Krej\u010dí Marta, \u010cermák Ale\u0161, Král Zden\u011bk, Mayer Ji\u0159í: Remission of the disease associated/related with immunoglobulin IgG4 accompanied by multiple lymphadenopathy after treatment with rituximab and dexamethasone: a case report. Vnit\u0159 Lék 2018, 64, 290. <https://doi.org/10.36290/vnl.2018.040>
Crossref Cited-by Linking logo