POEMS syndrome as an uncommon cause of papilledema / Carlos Mario Franco Echeverri    

Público ISBD Título : POEMS syndrome as an uncommon cause of papilledema Tipo de documento : documento electrónico Autores : Carlos Mario Franco Echeverri, Fecha de publicación : 2014 Títulos uniformes : Nepalese Journal of Ophthalmology Idioma : Inglés (eng) Palabras clave : POEMS syndrome  papilledema  vision disorders Resumen : 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. Mención de responsabilidad : C M Franco, K Balparda, A M Diaz, D Jiménez, A P Pamplona Referencia : Nepal J Ophthalmol. 2014 Jan;6(11):105-8. DOI (Digital Object Identifier) : 10.3126/nepjoph.v6i1.10781 PMID : 25341835 Derechos de uso : CC BY-NC-ND En línea : https://www.nepjol.info/index.php/NEPJOPH/article/view/10781 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3841 POEMS syndrome as an uncommon cause of papilledema [documento electrónico] / Carlos Mario Franco Echeverri,  . - 2014. Obra : Nepalese Journal of Ophthalmology Idioma : Inglés (eng) Palabras clave : POEMS syndrome  papilledema  vision disorders Resumen : 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. Mención de responsabilidad : C M Franco, K Balparda, A M Diaz, D Jiménez, A P Pamplona Referencia : Nepal J Ophthalmol. 2014 Jan;6(11):105-8. DOI (Digital Object Identifier) : 10.3126/nepjoph.v6i1.10781 PMID : 25341835 Derechos de uso : CC BY-NC-ND En línea : https://www.nepjol.info/index.php/NEPJOPH/article/view/10781 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3841

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