POEMS syndrome as an uncommon cause of papilledema
DOI:
https://doi.org/10.3126/nepjoph.v6i1.10781Keywords:
POEMS syndrome, papilledema, vision disordersAbstract
Background: Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is an uncommon condition related to a paraneoplastic syndrome secondary to an underlying plasma cell disorder. Among the myriad of manifestations of the disease, ocular signs and symptoms are relatively prevalent, affecting about half of all patients with the disease.
Objective: To report the ocular manifestations of POEMS syndrome.
Case: A 47-year-old lady diagnosed to have POEMS syndrome presented with painless progressive visual diminution. Her color vision was impaired. There was bilateral papilloedema.
Conclusion: POEMS syndrome should be considered among the differential diagnoses of all patients with a bilateral papilledema in which no other cause can be readily elucidated.
DOI: http://dx.doi.org/10.3126/nepjoph.v6i1.10781
Nepal J Ophthalmol 2014; 6 (2): 105-108
Downloads
Downloads
Published
How to Cite
Issue
Section
License
This license enables reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.