twitter
en POLSKI
eISSN: 2719-3209
ISSN: 0023-2157
Klinika Oczna / Acta Ophthalmologica Polonica
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
SCImago Journal & Country Rank
1/2008
vol. 110
 
Share:
Share:
abstract:
Case report

Orbital pseudotumor due to Ormond’s disease

Joanna Murawska
1
,
Paweł Lipowski
1
,
Krystyna Raczyńska
1

  1. Z Kliniki Chorób Oczu Akademii Medycznej w Gdańsku
Online publish date: 2008/03/17
View full text Get citation
 
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

Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.