Erdheim-Chester disease as differential diagnosis in bilateral exophthalmos

This report describes the case of a patient who had symmetrical exophthalmos, periorbital xanthelasmas and reduced vision. Next to Wegener's granulomatosis the differential diagnosis of Erdheim-Chester disease is discussed. It concerns a rare systemic histiocytosis of unknown etiology. Above al...

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Bibliographic Details
Published in:Klinische Monatsblätter für Augenheilkunde Vol. 221; no. 11; p. 960
Main Authors: Röpke, E, Herde, J, Bloching, M
Format: Journal Article
Language:German
Published: Germany 01-11-2004
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Summary:This report describes the case of a patient who had symmetrical exophthalmos, periorbital xanthelasmas and reduced vision. Next to Wegener's granulomatosis the differential diagnosis of Erdheim-Chester disease is discussed. It concerns a rare systemic histiocytosis of unknown etiology. Above all, the skeleton system with symmetrical long bone osteosclerosis is affected. Manifestations in the area of the orbit have seldom been reported with bilateral retrobulbar infiltrations, exophthalmos, diplopia, compression of the optic nerve and periorbital xanthelasmas.
ISSN:0023-2165
DOI:10.1055/s-2004-813771