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Hemorrhagic hypopyon as presenting feature of intravascular lymphoma, a case report.

Authors :
Winegarner A
Hashida N
Koh S
Nishida K
Source :
BMC ophthalmology [BMC Ophthalmol] 2017 Oct 25; Vol. 17 (1), pp. 195. Date of Electronic Publication: 2017 Oct 25.
Publication Year :
2017

Abstract

Background: Herpes uveitis has been previously reported to present with hyphema, but hemorrhagic hypopyon is rarely reported as a herpetic uveitis manifestation. We report a case of herpes simplex virus (HSV) presenting with hemorrhagic hypopyon, and speculate on the underlying pathophysiology with relation to an intravascular lymphoma which was subsequently diagnosed as a result.<br />Case Presentation: We present a case wherein a 62-year-old Japanese rheumatoid arthritis woman, with HSV uveitis, presented with hemorrhagic hypopyon in the anterior chamber and a fever with photophobia. Patient was treated with antiviral drugs which improved the hyphema and corneal lesions, but lesions recurred 3 months later. This rare presentation of HSV induced uveitis, and its subsequent recurrence, aroused suspicion of an additional hypopyon-inducing pathology. On account of previous history of lung opacities and elevated LDH, intravascular lymphoma was eventually diagnosed via lung biopsy. She was treated for the lymphoma which also completely resolved all ocular symptoms without any recurrence as of 1.5 years later.<br />Conclusion: The exceedingly rare presentation of hemorrhagic hypopyon may have been enabled by an interaction of the HSV with the intravascular lymphoma. HSV involvement was indicated by the dendritic lesions, IgG assay, and response to anti-viral drugs. The ocular involvement of the intravascular lymphoma seems to be indicated by virtue of the anti-tumor drugs completely resolving all ocular symptoms.

Details

Language :
English
ISSN :
1471-2415
Volume :
17
Issue :
1
Database :
MEDLINE
Journal :
BMC ophthalmology
Publication Type :
Academic Journal
Accession number :
29070018
Full Text :
https://doi.org/10.1186/s12886-017-0591-3