Hypocomplementaemic urticarial vasculitis syndrome presenting as unilateral dacryoadenitis
File version
Author(s)
Salonga-Reyes, Armi
Morris, Sharon
Griffith University Author(s)
Primary Supervisor
Other Supervisors
Editor(s)
Date
Size
File type(s)
Location
License
Abstract
Hypocomplementaemic urticarial vasculitis syndrome (HUVS) is rare and diagnostically challenging, with poten-tially severe multi-organ sequelae. To our knowledge this is the first report of HUVS presenting with dacryoadenitis. A 55-year-old Caucasian ex-tradesman presented to Emergency with a 12-day history of redness, swelling and blurred vision of his right eye. There was no history of trauma, foreign body, recent illness or overseas travel. He had a background of depression and migraines. Past ocular history was unremarkable. He smoked cigarettes, denied intravenous drug usage or venereal disease.
Journal Title
Clinical & Experimental Ophthalmology
Conference Title
Book Title
Edition
Volume
47
Issue
8
Thesis Type
Degree Program
School
Publisher link
Patent number
Funder(s)
Grant identifier(s)
Rights Statement
Rights Statement
Item Access Status
Note
Access the data
Related item(s)
Subject
Clinical sciences
Ophthalmology and optometry
Science & Technology
Life Sciences & Biomedicine
Ophthalmology
Persistent link to this record
Citation
Liong, RW; Salonga-Reyes, A; Morris, S, Hypocomplementaemic urticarial vasculitis syndrome presenting as unilateral dacryoadenitis, Clinical & Experimental Ophthalmology, 2019, 47 (8), pp. 1097-1101