Results 11 to 20 of about 305 (120)
, 2020 Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome is a rare disorder due to an underlying plasma cell clone (PC). The syndrome can affect several organs. The diagnosis is based on the presence of mandatory criteria (polyneuropathy, monoclonal plasma cell disorder) and at least one major and one minor ...
Meulemans, N +2 more
+7 more sources
Mymensingh medical journal : MMJ, 2011 A 49 years old male patient admitted with 2 years history of lower extremity symmetrical sensorimotor polyneuropathy, sclerodermic skin change, erectile dysfunction, hepatosplenomegaly and monoclonal gammopathy. The clinical evaluation met the criteria for the diagnosis of (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, skin ...
C R, Debnath +12 more
+7 more sources
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: 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
Unraveling unique features of plasma cell clones in POEMS syndrome with single-cell analysis
JCI Insight, 2022 POEMS syndrome is a rare monoclonal plasma cell disorder, with unique symptoms distinct from those of other plasma cell neoplasms, including high serum VEGF levels. Because the prospective isolation of POEMS clones has not yet been successful, their real
Yusuke Isshiki +20 more
doaj +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
Journal of Hematology & Oncology, 2018 Background POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome still has no standard treatment. On the basis that both POEMS syndrome and myeloma have an underlying plasma cell dyscrasia, anti-myeloma ...
Jinhuan Xu +14 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
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
Temporal dispersion in demyelination of POEMS syndrome and Castleman disease
Clinical Neurophysiology Practice, 2020 Objective: We detailed the electrophysiological patterns of peripheral nerve temporal dispersion across spectrum of POEMS syndrome and Castleman disease (CD).
Yue Hui Lau +4 more
doaj +1 more source