Results 81 to 90 of about 1,421,260 (161)
POEMS Syndrome: an Atypical Presentation with Chronic Diarrhoea and Asthenia
POEMS syndrome is a rare paraneoplastic condition associated with polyneuropathy, organomegaly, monoclonal gammopathy, endocrine and skin changes. We report a case of a man with Castleman disease and monoclonal gammopathy, with a history of chronic ...
Joana Alves Vaz +3 more
doaj +1 more source
POEMS syndrome: Case report [POEMS sendromu: Olgu sunumu]
Presented with characteristic polyneuropathy and multisystemic manifestations, POEMS syndrome is a rare plasma cell disorder. Vascular endothelial growth factor, secreted by plasmacytoma, is considered responsible for these symptoms.
Gökçay F. +5 more
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POEMS syndrome; a rare multi-systemic disorder that overlaps common conditions leading to confirmation bias [PDF]
This case highlights the tendency towards confirmation bias in patients with a new diagnosis of a rare disease, our patient’s signs and symptoms that arose from Scleroderma and its treatment obscured her presentation with POEMS syndrome.
Lacy, Mary, Almaraz, Karla B
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POEMS syndrome with IgA lambda monoclonal gammopathy
The various association of polyneuropathy, organomegaly, endocrinopathy, monoclonal protein and skin changes has been called the POEMS syndrome. Herein we report a case in which all the typical clinical and laboratory findings of the POEMS syndrome were ...
G. Piccolo +5 more
core +1 more source
Non-POEMS osteosclerotic multiple myeloma: Clinical characteristics and differential diagnosis
Osteosclerosis in multiple myeloma (MM) is typically associated with rare POEMS syndrome, characterized by polyneuropathy (P), organomegaly (O), endocrinopathy (E), M-protein (M), and skin changes (S).
Zi-Yan Li +5 more
doaj +1 more source
Recurrent Transient Ischemic Attacks in a Patient with POEMS Syndrome
A 47-year-old female with a prior history of POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome was admitted with transient ischemic attacks complicated by dysarthria and right-sided hemiparesis.
B. Nazliel +9 more
core +1 more source
Raised VEGF: High sensitivity and specificity in the diagnosis of POEMS syndrome [PDF]
Objective: To investigate the sensitivity and the specificity of serum vascular endothelial growth factor (sVEGF) for the diagnosis of polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome in patients with a ...
Pihan, M +6 more
core +1 more source
POEMS syndrome with acute kidney injury:a case report and literature review
Objective The major clinical manifestations of POEMS syndrome are polyneuropathy,organomegaly,endocrinopathy,monoclonal gammopathy,and skin changes,but its complication with kidney injure is rare.To analyze the clinical characteristics and prognosis of ...
WANG Yan, ZHOU Le, LI Wei
doaj
A Rare Case of Castleman Variant of POEMS Syndrome
POEMS syndrome is a rare multisystemic disease, characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes. The presence of polyneuropathy and monoclonal plasma cell proliferation is mandatory for the diagnosis of
Gevesh Chand Dewangan +3 more
doaj +1 more source
Papilledema with POEMS Syndrome
Optic disc swelling has been described in some patients with POEMS Syndrome (Polineuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes). The pathogenesis of optic disc swelling is still controversial.
S. Bianchi-Manzoli, MD; P. Ciasca; C. Rojo; F. Carones; R. Brancato
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