Results 161 to 170 of about 26,946 (207)
Recurrent brain infarction as the first manifestation of POEMS syndrome
Chinese Journal of Contemporary Neurology and NeurosurgeryWANG Yan⁃yan +3 more
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From hepatomegaly to POEMS syndrome: A case report. [PDF]
Hepatol ForumOzden Y, Gursoy S.
europepmc +1 more source
Case report: DKRd regimen in the treatment of newly diagnosed POEMS syndrome and literature review. [PDF]
Front OncolWang J, Liao W, Liu Z, Kong D.
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Plasma cell and neutrophil enriched neovascularization with granulomatous lymphangitis in POEMS syndrome. [PDF]
JAAD Case RepAdeuyan O +7 more
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The American Journal of the Medical Sciences, 2023
POEMS-syndrome (polyneuropathy — P, organomegaly — O, endocrinopathy — E, M-protein — M, skin changes — S) is a paraneoplastic syndrome caused by underlying dyscrasia of plasma cells. The main criteria of the syndrome are polyradiculoneuropathy, clonal proliferation of plasma cells, sclerotic bone lesions, elevated levels of vascular endothelial growth
Xin, Dong, Rui, Jing, Jun, Li
openaire +4 more sources
POEMS-syndrome (polyneuropathy — P, organomegaly — O, endocrinopathy — E, M-protein — M, skin changes — S) is a paraneoplastic syndrome caused by underlying dyscrasia of plasma cells. The main criteria of the syndrome are polyradiculoneuropathy, clonal proliferation of plasma cells, sclerotic bone lesions, elevated levels of vascular endothelial growth
Xin, Dong, Rui, Jing, Jun, Li
openaire +4 more sources
Seminars in Dermatology, 1995
The principal features of POEMS syndrome are osteosclerotic bone lesions, peripheral sensorimotor neuropathy, and elevated levels of a monoclonal protein in the serum or urine. Skin lesions are present in the majority of patients with POEMS syndrome. Diffuse hyperpigmentation is the most common cutaneous finding.
C, Dieckmann, V, Nicolas
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The principal features of POEMS syndrome are osteosclerotic bone lesions, peripheral sensorimotor neuropathy, and elevated levels of a monoclonal protein in the serum or urine. Skin lesions are present in the majority of patients with POEMS syndrome. Diffuse hyperpigmentation is the most common cutaneous finding.
C, Dieckmann, V, Nicolas
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Pathology, 1991
A 40 year old Chinese woman presented with anasarca and later developed features of POEMS syndrome. These are peripheral neuropathy (P), organomegaly (O), endocrine dysfunction (E), monoclonal gammopathy (M), and skin changes (S) which are usually associated with plasma cell dyscrasia.
N W, Leung, C W, Lam, J C, Pang
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A 40 year old Chinese woman presented with anasarca and later developed features of POEMS syndrome. These are peripheral neuropathy (P), organomegaly (O), endocrine dysfunction (E), monoclonal gammopathy (M), and skin changes (S) which are usually associated with plasma cell dyscrasia.
N W, Leung, C W, Lam, J C, Pang
openaire +2 more sources
La Presse Médicale
POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, Skin changes) is a syndrome that involves a monoclonal B-cell proliferation, most often plasmacytic, and a variable number of manifestations listed or not in the acronym.
Arnaud Jaccard +3 more
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POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, Skin changes) is a syndrome that involves a monoclonal B-cell proliferation, most often plasmacytic, and a variable number of manifestations listed or not in the acronym.
Arnaud Jaccard +3 more
openaire +3 more sources