IgG4-related Diseases - A Rare Polycystic Form of Ormond's Disease
Jazyk angličtina Země Česko Médium print
Typ dokumentu kazuistiky, časopisecké články
PubMed
27668529
DOI
10.14712/23362936.2016.13
PII: pmr_2016117020124
Knihovny.cz E-zdroje
- Klíčová slova
- Ormond’s disease, Polycystic form, Retroperitoneal fibrosis,
- MeSH
- imunoglobulin G * MeSH
- lidé středního věku MeSH
- lidé MeSH
- počítačová rentgenová tomografie MeSH
- retroperitoneální fibróza diagnóza patologie chirurgie MeSH
- retroperitoneální prostor patologie MeSH
- urologické chirurgické výkony MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Názvy látek
- imunoglobulin G * MeSH
Currently, Ormond's disease is classified among IgG4-associated diseases. Its clinical manifestation varies and is characterized by the presence of fibrous retroperitoneal tissue that often affects the ureters or abdominal aorta and iliac arteries. We present a unique case of the polycystic form of Ormond's disease, imitating tumour in the retroperitoneal space. At the time of diagnosis, the disease was not metabolically active and did not require immunosuppressive therapy. The polycystic mass was removed surgically. There has been no exacerbation of the disease during the last 12 months.
Department of Pathology Na Homolce Hospital Prague Czech Republic
Department of Vascular Surgery Na Homolce Hospital Prague Czech Republic
Citace poskytuje Crossref.org
