Current issue
Archive
Videos
Articles in press
About the journal
Supplements
Editorial board
Reviewers
Abstracting and indexing
Subscription
Contact
Instructions for authors
Publication charge
Ethical standards and procedures
Editorial System
Submit your Manuscript
|
1/2008
vol. 110 abstract:
Case report
Orbital pseudotumor due to Ormond’s disease
Joanna Murawska
1
,
Paweł Lipowski
1
,
Krystyna Raczyńska
1
Online publish date: 2008/03/17
View
full text
Get citation
ENW EndNote
BIB JabRef, Mendeley
RIS Papers, Reference Manager, RefWorks, Zotero
AMA
APA
Chicago
Harvard
MLA
Vancouver
Retroperitoneal fibrosis (RPF) is characterized by the presence of a fibro-inflammatory tissue, which usually surrounds the abdominal aorta and the iliac arteries and extends into the retroperitoneum. Up to 15% of patients have additional fibrotic processes outside the retroperitoneum. Retroperitoneal fibrosis is generally idiopathic, but can also be secondary to the use of certain drugs, malignant diseases, infections and surgery. The etiology of idiopathic retroperitoneal fibrosis, so called „Ormond’s disease”, remains unknown.
In this study we present the 54 years old woman with orbital pseudotumour of right lacrimal gland associated with retroperitoneal fibrosis. Diagnosis was confirmed with computed tomography of abdominal cavity and orbit. Needle biopsy from the tumour in the orbit revealed only fibrous tissue with signs of chronic inflammation. Together with typical findings of an idiopathic retroperitoneal fibrosis, the final diagnosis of Ormond’s disease with orbital pseudotumorous fibrosis was made. It is important that both, the ophthalmologist and the urologist are aware of the existence of this association, so that suitable treatment can be initiated without delay. keywords:
idiopathic retroperitoneal fibrosis, orbital pseudotumor, Ormond’s disease |
|