机构:
Univ Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, AustraliaUniv Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, Australia
Fung, S
[1
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Selva, D
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机构:
Univ Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, AustraliaUniv Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, Australia
Selva, D
[1
]
Leibovitch, I
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Univ Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, AustraliaUniv Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, Australia
Leibovitch, I
[1
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Hsuan, J
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Univ Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, AustraliaUniv Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, Australia
Hsuan, J
[1
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Crompton, J
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Univ Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, AustraliaUniv Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, Australia
Crompton, J
[1
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机构:
[1] Univ Adelaide, Royal Adelaide Hosp, Dept Ophthalmol, Oculoplast & Orbital Unit, Adelaide, SA 5000, Australia
Purpose: To describe ophthalmic manifestations in a series of patients with multiple myeloma ( MM) and review the literature. Design: Retrospective case series. Methods: Review of all cases with ophthalmic manifestations of MM seen at the Department of Ophthalmology, Royal Adelaide Hospital, between 1987 and 2002. Results: Of all patients with MM who were managed at the Royal Adelaide Hospital in the study period, only 8 were referred to the Ophthalmology Department with ophthalmic manifestations. Five males and 3 females with a mean age of 61.25 years ( range 42 - 78) who exhibited ophthalmic manifestations were studied. Six patients (75%) had known MM at the time of their ophthalmic evaluation. Four patients (50%) had neuro-ophthalmic symptoms resulting in diplopia or visual disturbances. Three patients (37.5%) presented with orbital involvement and 1 (12.5%) with hyperviscosity retinopathy. Five patients (62.5%) died within 2 months of their ophthalmic presentation. Conclusion: Ophthalmic manifestations of MM are uncommon and diverse. They may appear at the initial presentation of the disease or occur late in the disease process. Awareness of the possible manifestations may lead to an earlier diagnosis and have a positive influence on the disease course. Copyright (C) 2005 S. Karger AG, Basel.
机构:
Boston Univ, Sch Med, Dept Ophthalmol, Boston, MA 02118 USABoston Univ, Sch Med, Dept Ophthalmol, Boston, MA 02118 USA
Kefella, Haben
Luther, Daniel
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Boston Univ, Sch Med, Dept Ophthalmol, Boston, MA 02118 USABoston Univ, Sch Med, Dept Ophthalmol, Boston, MA 02118 USA
Luther, Daniel
Hainline, Clotilde
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Boston Univ, Sch Med, Dept Ophthalmol, Boston, MA 02118 USA
Boston Univ, Sch Med, Dept Neurol, 72 East Concord St,Neurol C-3, Boston, MA 02118 USABoston Univ, Sch Med, Dept Ophthalmol, Boston, MA 02118 USA