Lacrimal gland enlargement as one of the ocular manifestations of Wegener's granulomatosis

1985 ◽  
Vol 59 (1) ◽  
pp. 21-26 ◽  
Author(s):  
R. J. Boukes ◽  
W. A. E. J. De Vries-Knoppert
Orbit ◽  
1985 ◽  
Vol 4 (3) ◽  
pp. 163-175 ◽  
Author(s):  
R. J. Boukes ◽  
P. J. Kruit ◽  
A. Th. M. van Balen ◽  
L. Koornneef ◽  
R. de Slegte

2011 ◽  
Vol 6 (5) ◽  
pp. 541-555 ◽  
Author(s):  
Hazlita Isa ◽  
Susan Lightman ◽  
Charles D Pusey ◽  
Simon RJ Taylor

1984 ◽  
Vol 98 (6) ◽  
pp. 736-740 ◽  
Author(s):  
Tetsuro Koyama ◽  
Nobuhiko Matsuo ◽  
Yoshimasa Watanabe ◽  
Makoto Ojima ◽  
Takumi Koyama

1977 ◽  
Vol 63 (1) ◽  
pp. 131-141 ◽  
Author(s):  
Barton F. Haynes ◽  
Martin L. Fishman ◽  
Anthony S. Fauci ◽  
Sheldon M. Wolff

2003 ◽  
Vol 117 (2) ◽  
pp. 148-150 ◽  
Author(s):  
S. Y. Liu ◽  
A. C. Vlantis ◽  
W. C. Lee

Wegener’s granulomatosis is a potentially fatal disease of unknown origin affecting mainly the upper and lower respiratory tracts and kidneys. Prompt recognition of the more unusual presentations of the disease is necessary to ensure early treatment. We present a case of a 46-year-old female with bilateral submandibular and parotid gland enlargement.Parotid or submandibular salivary gland enlargement is a rare presenting feature of Wegener’s granulomatosis. Common to 80 per cent of these cases is nasal involvement, while ear pathology or lung lesions may occur in the remaining cases. The diagnosis is both clinical and pathological, biopsy of suspicious tissue, serum c-ANCA levels and a chest X-ray are valuable investigations. Treatment with immunosuppressive therapy is essential, and usually ensures a long-term remission.


1995 ◽  
Vol 16 (2) ◽  
pp. 119-122 ◽  
Author(s):  
John T. Lanza ◽  
Yuan Ku ◽  
Frank E. Lucente ◽  
Gady Har-El

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