Results 1 to 10 of about 2,670,869 (240)

POEMS syndrome in the 21st century: A bibliometric analysis [PDF]

Heliyon, 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, Zhimin Wu, Shanyi Sun, Yunfeng Fu, Yi Chen, Jing Liu   +5 more
doaj   +5 more sources

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

Scientific 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, Shokichi Tsukamoto, Naoya Mimura, Yurie Miyamoto-Nagai, Yusuke Isshiki, Shinichiro Matsui, Sanshiro Nakao, Asuka Shibamiya, Yutaro Hino, Kensuke Kayamori, Nagisa Oshima-Hasegawa, Tomoya Muto, Yusuke Takeda, Tomoki Suichi, Sonoko Misawa, Chikako Ohwada, Koutaro Yokote, Satoshi Kuwabara, Chiaki Nakaseko, Hiroyuki Takamatsu, Emiko Sakaida   +20 more
doaj   +3 more sources

Castleman disease variant of POEMS syndrome without M protein: a case report [PDF]

Frontiers in Oncology
POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) syndrome is a paraneoplastic syndrome associated with an underlying plasma cell neoplasm. According to the current diagnostic criteria for POEMS syndrome, the presence
Min Ji, Shumin Jin, Shaolei Zang, Peng Li, Fei Lu, Chuanli Zhao, Chunqing Zhang, Chunyan Ji, Jingjing Ye   +8 more
doaj   +3 more sources

Case report: Atypical POEMS syndrome without polyneuropathy, complicated by borderline TAFRO syndrome [PDF]

Frontiers in Medicine
POEMS syndrome is a complex and rare hematological disease involving multiple physiological systems. According to the currently accepted diagnostic criteria for POEMS syndrome, polyneuropathy is one of the primary mandatory criteria.
Shuai Tan, Mingyue Shang, Yasufumi Masaki, Jing Ni, Yuwei Da, Jing Sun, Yaofang Cao, Li Su, Wanling Sun   +8 more
doaj   +3 more sources

Case report: POEMS syndrome masquerades as diabetic foot. [PDF]

Front Neurol, 2023
We present the case of a 54-year-old woman with reasonable blood sugar control who presented with a diabetic foot combined with severe peripheral neuropathy and vascular disease.
Zhou GX, Xiao L, Bi YM, Yang F, Yang CZ, Zhang D.   +5 more
europepmc   +2 more sources

Capillary leak phenotype as a major cause of death in patients with POEMS syndrome. [PDF]

Leukemia
Cause of death (COD) in POEMS (polyneuropathy, organomegaly, endocrinopathies, monoclonal protein and skin changes) syndrome is not well described. We investigated COD in patients with POEMS syndrome treated at Mayo Clinic between 2000 and 2022.
Lee K, Kourelis T, Tschautscher M, Warsame R, Buadi F, Gertz M, Muchtar E, Dingli D, Hayman S, Go R, Hwa L, Fonder A, Gonsalves W, Hobbs M, Kyle R, Kapoor P, Leung N, Binder M, Cook J, Lin Y, Rogers M, Rajkumar SV, Kumar S, Dispenzieri A.   +23 more
europepmc   +2 more sources

Unraveling unique features of plasma cell clones in POEMS syndrome with single-cell analysis

JCI Insight, 2022
POEMS syndrome is a rare monoclonal plasma cell disorder, with unique symptoms distinct from those of other plasma cell neoplasms, including high serum VEGF levels. Because the prospective isolation of POEMS clones has not yet been successful, their real
Yusuke Isshiki, Motohiko Oshima, Naoya Mimura, Kensuke Kayamori, Yurie Miyamoto-Nagai, Masahide Seki, Yaeko Nakajima-Takagi, Takashi Kanamori, Eisuke Iwamoto, Tomoya Muto, Shokichi Tsukamoto, Yusuke Takeda, Chikako Ohwada, Sonoko Misawa, Jun-ichiro Ikeda, Masashi Sanada, Satoshi Kuwabara, Yutaka Suzuki, Emiko Sakaida, Chiaki Nakaseko, Atsushi Iwama   +20 more
doaj   +2 more sources

POEMS syndrome with undetectable M-protein: a case report and literature review

Diagnostic Pathology
Background Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is a rare plasma cell (PC) neoplasm with associated paraneoplastic syndrome. According to the current diagnostic criteria, peripheral polyneuropathy and
Han-Yue Xue, Lin Zhou, Qin-Zhao Yuan, Yang Zhang, Yi-Qun Hao, Shao-Wei Chen, Hong-Kun Wang, Fang Wei   +7 more
doaj   +2 more sources

From hepatomegaly to POEMS syndrome: A case report. [PDF]

Hepatol Forum
We present a case of POEMS syndrome from Turkiye, a rare, multisystemic condition resulting from plasma cell dyscrasia. POEMS is an acronym representing its cardinal features: Peripheral neuropathy; Organomegaly; Endocrinopathy; Monoclonal plasma-cell ...
Ozden Y, Gursoy S.
europepmc   +2 more sources

POEMS SYNDROME

Zdravniški Vestnik, 2008
BACKGROUND We have presented the patient with POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, M protein, Skin changes) in which peripheral neuropathy wasassociated with monoclonal gammopathy and osteosclerotic myeloma.
Bojana Luštrek, Peter Černelč
doaj   +6 more sources