Results 31 to 40 of about 2,670,869 (240)
Current Opinion in Neurology, 2018 Purpose of review To provide an overview of polyneuropathy organomegaly endocrinopathy M-protein and skin changes (POEMS) syndrome, detailing new insights into pathogenesis, prognostic factors, treatments, and outcome scores. Recent findings With the development of large multicentre
Keddie, S, Lunn, MP
openaire +5 more sources
Daratumumab monotherapy for relapsed POEMS syndrome
American journal of hematology/oncology, 2023 To the Editor: POEMS (Polyneuropathy, Organomegaly, Endocrinopathies, Monoclonal protein, Skin changes) syndrome is a rare paraneoplastic manifestation related to an underlying plasma cell neoplasm.
D. Dima, J. Valent, Jack Khouri
semanticscholar +1 more source
POEMS syndrome: origination from clonal plasma cells or B cells?
Hematology, 2023 Objectives POEMS syndrome is a rare disorder which has been increasingly recognized. The clonal origin is controversial. Some people argue that POEMS syndrome originates from abnormal plasma cell clones.
Lu Zhou +8 more
doaj +1 more source
POEMS neuropathy: optimising diagnosis and management [PDF]
, 2018 POEMS syndrome is a rare and disabling autoinflammatory condition characterised by a typical peripheral neuropathy and the presence of a monoclonal plasma cell disorder.
Carr, AS +5 more
core +1 more source
Missed diagnosis of POEMS syndrome with onset of progressive fatigue and numbness: a case report
Journal of International Medical Research, 2021 POEMS syndrome is a rare multisystem disease associated with an underlying plasma cell disorder. Its name is an acronym for peripheral neuropathy (P), endocrinopathy (E), organomegaly (O), monoclonal plasma cell proliferative disorder (M), and skin ...
Huan Shi +3 more
doaj +1 more source
POEMS syndrome misdiagnosed as CIDP: A case report [PDF]
Balneo and PRM Research Journal, 2023 POEMS syndrome is a paraneoplastic disorder manifested by peripheral neuropathy and monoclonal plasma cell dyscrasia. Due to its clinical and electrophysiological aspect, POEMS syndrome is often mistaken as a chronic inflammatory demyelinating ...
Vitalie Văcăraș +4 more
doaj +1 more source
POEMS Syndrome in a 20-year-old Patient Diagnosed Following a Complaint of Reduced Visual Acuity [PDF]
, 2014 We report a case of POEMS syndrome in a 20-year-old patient diagnosed after visiting an eye clinic with a chief complaint of reduced visual acuity. A male university student aged 20 years was referred to our department complaining of blurred vision in ...
Doi, Shinichiro +8 more
core +1 more source
Successful treatment with bortezomib for POEMS syndrome, overcoming complicated severe heart block
Clinical Case Reports, 2023 Cardiac bradyarrhythmia and conduction disorder may be rare, but recurrent adverse events caused by bortezomib. Here we report a case with POEMS syndrome presenting severe heart block after bortezomib plus dexamethasone therapy. After permanent pacemaker
Yuichi Nakamura +5 more
semanticscholar +1 more source
Journal of International Medical Research, 2021 POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) syndrome is rare, with polyneuropathy and monoclonal plasma cell disorder generally considered as essential diagnostic symptoms.
Hua Ping Du +3 more
doaj +1 more source
Longitudinal bioimpedance assessments to evaluate hydration in POEMS syndrome [PDF]
, 2016 Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes (POEMS) syndrome is a rare paraneoplastic disorder associated with an underlying plasma cell dyscrasia and multiorgan failure.
Barbosa-Silva +8 more
core +2 more sources