Results 31 to 40 of about 26,946 (207)

POEMS syndrome misdiagnosed as diabetic peripheral neuropathy: A case report

open access: yesJournal of Clinical and Translational Endocrinology Case Reports, 2022
POEMS syndrome is a rare paraneoplastic syndrome caused by potential plasma cell diseases. It is mainly manifested as polyneuropathy and monoclonal plasma cell-proliferative disorder, may also be accompanied by Castleman diseases, sclerosing bone lesions,
Jiaojiao Yang   +2 more
doaj   +1 more source

POEMS SYNDROME: AN UPDATE [PDF]

open access: yesMediterranean Journal of Hematology and Infectious Diseases, 2017
POEMS syndrome is a rare, chronic and disabling condition. The causes of this condition remain unknown; however, chronic overproduction of pro-inflammatory cytokines appears to be a major contributor. Early diagnosis is essential to start treatment before the clinical condition of the patient becomes compromised.A complete evaluation of the disease at ...
openaire   +3 more sources

POEMS syndrome with extensive calciphylaxis: A case report and literature review

open access: yesIndian Journal of Dermatology, 2020
POEMS syndrome, a paraneoplastic disorder, caused by plasma cell dyscrasia, is characterized by polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes.
Cheng-Han Liu   +4 more
doaj   +1 more source

Peripheral retinal leakage in POEMS syndrome

open access: yesInternational Journal of Retina and Vitreous, 2021
Background POEMS (polyneuropathy, organomegaly, endocrinopathy, myeloma protein, skin changes) syndrome is a rare blood disorder with multi-system involvement. The cause is unknown.
Andrew Rising Carey, Praveen Jeyaseelan
doaj   +1 more source

Lenalidomide and Dexamethasone for a Patient of POEMS Syndrome Presenting with Massive Ascites

open access: yesCase Reports in Hematology, 2014
POEMS syndrome is a multisystem disorder characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. POEMS syndrome is a rare cause of refractory ascites.
Shuji Ueda   +11 more
doaj   +1 more source

Polyneuropathy as Novel Initial Manifestation in a Case of “Nonsecretory” POEMS Syndrome with Sjögren’s Syndrome

open access: yesCase Reports in Medicine, 2017
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is a paraneoplastic syndrome driven by plasma cell dyscrasias.
Minrui Liang   +6 more
doaj   +1 more source

Raynaud’s phenomenon and positive antinuclear antibodies as first manifestation of POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes): a case report

open access: yesBMC Rheumatology, 2022
Background POEMS syndrome is a rare paraneoplastic syndrome caused by plasma cell disorder almost always lambda restricted. Secondary Raynaud’s phenomenon is an overlooked skin manifestation of the disease even though it is present in twenty percent of ...
Fabio Torres-Saavedra, Lina León-Sierra
doaj   +1 more source

Culture: Not just Burns – what about the poet Robert Fergusson? [PDF]

open access: yes, 2016
No abstract ...
Bismarck F Hernández-Álvarez   +8 more
core   +3 more sources

Detection of clonal plasma cells in POEMS syndrome using multiparameter flow cytometry

open access: yesScientific Reports
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein [M-protein], and skin changes) is a rare systemic disorder characterized by various symptoms caused by underlying plasma cell (PC) dyscrasia.
Arata Ishii   +20 more
doaj   +1 more source

Clinical and biochemical characteristics for patients with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome: a pilot observational study

open access: yesFrontiers in Neurology
BackgroundPolyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is rare life-threatening condition associated with a clonal plasma cell neoplasm.ObjectiveThe aim of this study is to investigate the clinical and ...
Pei Li   +8 more
doaj   +1 more source

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