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(organomegaly)
1,379 results
  • Neuro-ophthalmological manifestations of POEMS syndrome. [Journal Article]
    Arch Soc Esp Oftalmol 2019Ortiz Zapata A, Cárdenas PL, … Pizarro Imaicela B
  • The cases is presented of a 38 year-old male with a constitutional syndrome, fever, multiple swollen lymph nodes, and hepatosplenomegaly of 2 months onset. There was also mention of headache, bilateral blurred vision, and myiodesopsias. Best correct visual acuity was 20/50 and 20/200. The anterior segment was unremarkable. The fundus of both eyes showed raised and erased discs, accompanied by ser…
  • POEMS syndrome complicated by ischaemic stroke and cerebral vasculitis. [Journal Article]
    BMJ Case Rep 2019; 12(7)Vasilevskiy L, Akhondi H, Wierman A
  • We present a case of ischaemic stroke in the context of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome associated with cerebral vasculitis as confirmed by imaging. There is little information on the prevalence of cerebral vasculitis in POEMS patients, and we found only one previous report of such case in the literature.
  • Characteristics of 1946 Cases of POEMS Syndrome in Chinese Subjects: A Literature-Based Study. [Systematic Review]
    Front Immunol 2019; 10:1428Wang Y, Huang LB, … Wang Y
  • POEMS syndrome is a rare paraneoplastic disorder characterized secondary to a rare plasma cell dyscrasia. Here, we aimed to analyze the clinical characteristics of large sample cases of POEMS in Chinese subjects through making a review of the Chinese literature. Four databases were electronically searched from inception until October 2016. Case reports and case series were identified. Six hundred…
  • [An unusual case of POEMS syndrome: in absence of clinical sign of polineuropathy.] [Journal Article]
    Recenti Prog Med 2019; 110(6):302-305Vainieri AFM, Morelli S
  • POEMS syndrome (P polyradiculoneuropathy, O organomegaly, E endocrinopathy, M clonal plasma cell disorder, and S skin changes) is a rare syndrome due to a plasma cell dyscrasia. It is characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, skin changes. Increased serum VEGF, sclerotic bone lesions, Castleman's disease, oedema, ascites, papilledema and thrombocytosis …
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