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POEMS syndrome: A rare entity

open access: yesIndian Journal of Pathology and Microbiology, 2023
POEMS syndrome is a rare paraneoplastic syndrome due to an underlying plasma cell disorder. The diagnosis of POEMS syndrome can be a challenge. A good history, physical examination, and appropriate testing can aid in establishing its diagnosis.
Chaganti P. Devi   +4 more
doaj   +2 more sources

POEMS syndrome in the 21st century: A bibliometric analysis

open access: yesHeliyon, 2023
Background: POEMS syndrome is a rare and complex plasma cell disorder characterized by polyneuropathy, organomegaly, endocrinopathy, high M protein levels, and skin changes.
Fangrong Zhang   +5 more
doaj   +3 more sources

Atypical presentation of intraosseous plasmacytoma in a patient with POEMS syndrome [PDF]

open access: yesRadiology Case Reports
POEMS syndrome is an uncommon paraneoplastic syndrome featuring polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. POEMS syndrome in conjunction with plasmacytoma is a particularly rare finding, mostly featured only in
Jude Kolodisner, BS   +3 more
doaj   +2 more sources

A rare case of POEMS syndrome with unique endoscopic presentation [PDF]

open access: yesAnnals of Hematology
POEMS (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy, Skin changes) syndrome is a rare multisystem disease, often presenting diagnostic challenges.
Jing-kai Zhou   +6 more
doaj   +2 more sources

Fulminant Evans syndrome and splenic infarction as initial manifestations of POEMS syndrome with monoclonal kappa light chain restriction: a diagnostic and therapeutic challenge [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine
Introduction: Autoimmune cytopenias have been very rarely reported in conjunction with POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome).
Mohamed Reda Belkhribchia   +6 more
doaj   +2 more sources

POEMS syndrome with multiple ganglioside/paraneoplastic antibodies misdiagnosed as CIDP: a case report [PDF]

open access: yesFrontiers in Oncology
POEMS syndrome is a rare multisystem disorder characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal protein (M-protein) secretion, and skin changes.
Mengmeng Fan   +4 more
doaj   +2 more sources

Delayed diagnosis of POEMS syndrome, how AI tools can enhance diagnostic accuracy [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine
Polyneuropathy, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes (POEMS) syndrome is a rare multisystem disorder often misdiagnosed due to its wide-ranging manifestations and clinical overlap with common medical conditions.
Max Jin   +4 more
doaj   +2 more sources

High-Resolution Nerve Ultrasound Abnormalities in POEMS Syndrome—A Comparative Study

open access: yesDiagnostics, 2021
Background: High-resolution nerve ultrasound (HRUS) has been proven to be a valuable tool in the diagnosis of immune-mediated neuropathies, such as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).
Marc Dörner   +10 more
doaj   +1 more source

Better prognosis in POEMS patients with cerebral infarction before polyneuropathy

open access: yesHeliyon, 2022
POEMS syndrome is a plasma cell disease. Clinical manifestations and clinical onset are variable. In recent years, more and more cases of POEMS syndrome with cerebrovascular disease and ischemic stroke have been reported. However, it is rare for patients
Xiaoxi Lan   +5 more
doaj   +1 more source

CASTLEMAN DISEASE VARIANT OF POEMS SYNDROME: A CASE REPORT AND LITERATURE REVIEW [PDF]

open access: yes精准医学杂志, 2023
Objective To improve the awareness of POEMS syndrome among clinicians, and to increase the experience in the clinical diagnosis and treatment of atypical POEMS syndrome.
LI Yuxin, XU Xiang, ZHANG Xiaolin, XING Baodi, ZHAO Wenjuan, HAO Dapeng, LIU Bin, CHEN Yunqing, DONG Bingzi, WANG Zhongchao, SUN Xiaofang, ZHAO Yuhang
doaj   +1 more source

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