Results 21 to 30 of about 2,670,869 (240)
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
+6 more sources
High-Resolution Nerve Ultrasound Abnormalities in POEMS Syndrome—A Comparative Study
Diagnostics, 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
Heliyon, 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]
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
POEMS syndrome: Update on diagnosis, risk‐stratification, and management
American journal of hematology/oncology, 2023 POEMS syndrome is a life‐threatening condition due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyradiculoneuropathy, clonal plasma cell disorder, sclerotic bone lesions, elevated vascular endothelial growth factor ...
A. Dispenzieri
semanticscholar +1 more source
Indian 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 +1 more source
Clinical spectrum of POEMS-associated multicentric Castleman disease with renal involvement: a diagnostic challenge [PDF]
Journal of Nephropathology, 2019 Background: Castleman disease (CD) is a rare and heterogeneous lymphoproliferative disorder with a wide variety of clinical presentations and outcomes.
Caroline Kullmann Ribeiro +5 more
doaj +1 more source
Culture: Not just Burns – what about the poet Robert Fergusson? [PDF]
, 2016 No abstract ...
Bismarck F Hernández-Álvarez +8 more
core +3 more sources
Blood Cancer Journal, 2023 INTRODUCTION POEMS (Polyneuropathy, Organomegaly, Endocrinopathies, Monoclonal protein, Skin changes) syndrome is a rare paraneoplastic syndrome related to plasma cell disorders. The diagnosis is often delayed, and many patients are diagnosed and treated
I. Vaxman +21 more
semanticscholar +1 more source
POEMS syndrome: 2021 Update on diagnosis, risk‐stratification, and management
American journal of hematology/oncology, 2021 POEMS syndrome is a paraneoplastic syndrome due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyradiculoneuropathy, clonal plasma cell disorder (PCD), sclerotic bone lesions, elevated vascular endothelial growth factor,
A. Dispenzieri
semanticscholar +1 more source