Results 21 to 30 of about 1,326,560 (112)

Pulmonary manifestations of POEM syndrome: a retrospective analysis of 282 cases

BMC Pulmonary Medicine, 2023
Background Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a rare multisystemic clonal plasma cell disorder.
Yilin Huang, Yang Luo, Huan Hou, Jinming Gao   +3 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, Fernanda Bresciani, Samile Echeverria Silveira, Pedro Guilherme Schaefer, Elvino Guardão Barros, Francisco Veríssimo Veronese   +5 more
doaj   +1 more source

POEMS Syndrome: Latest Comprehensive Review

, 2023
Latar Belakang: Sindrom POEMS meliputi polineuropati, organomegali, endokrinopati, protein M, dan perubahan kulit. Sindrom POEMS merupakan kelainan langka dengan usia rata-rata onset antara 46 dan 56 tahun.
Teresia, Vira, Geraldine Arliska, Vira, Setio, Lisa, Efranisa S B, Ririn, Alvionita Wongso, Clara   +4 more
core   +1 more source

POEMS syndrome misdiagnosed as diabetic peripheral neuropathy: A case report

Journal of Clinical and Translational Endocrinology Case Reports, 2022
POEMS syndrome is a rare paraneoplastic syndrome caused by potential plasma cell diseases. It is mainly manifested as polyneuropathy and monoclonal plasma cell-proliferative disorder, may also be accompanied by Castleman diseases, sclerosing bone lesions,
Jiaojiao Yang, Jianjian Zhang, Jianmin Ren   +2 more
doaj   +1 more source

Successful Weaning after Plasma Exchange for Polyneuropathy Related to Poems Syndrome

, 2011
Respiratory failure due to polyneuropathy associated with POEMS syndrome (Polyneuropathy, organomegaly. endocrinopathy , M protein, and skin changes) is unusual.
吳尚俊;郭炳宏;楊泮池, WU, SHANG-GIN;KUO, PING-HUNG;YANG, PAN-CHYR   +1 more
core   +1 more source

Lenalidomide and Dexamethasone for a Patient of POEMS Syndrome Presenting with Massive Ascites

Case Reports in Hematology, 2014
POEMS syndrome is a multisystem disorder characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. POEMS syndrome is a rare cause of refractory ascites.
Shuji Ueda, Sayoko Yonemoto, Kazumasa Oka, Naohiko Fujii, Keiichi Nakata, Hitomi Matsunaga, Seiko Kataoka, Yuki Iwama, Hiroyuki Narahara, Yuichi Yasunaga, Yoshiaki Inui, Sumio Kawata   +11 more
doaj   +1 more source

POEMS syndrome with extensive calciphylaxis: A case report and literature review

Indian Journal of Dermatology, 2020
POEMS syndrome, a paraneoplastic disorder, caused by plasma cell dyscrasia, is characterized by polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes.
Cheng-Han Liu, Yu-Chen Chen, Tsai-Yun Chen, Hang-Wei Huang, Julia Yu-Yun Lee   +4 more
doaj   +1 more source

Polyneuropathy as Novel Initial Manifestation in a Case of “Nonsecretory” POEMS Syndrome with Sjögren’s Syndrome

Case Reports in Medicine, 2017
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is a paraneoplastic syndrome driven by plasma cell dyscrasias.
Minrui Liang, Zhixing Jiang, Zhiguang Lin, Bobin Chen, Hejian Zou, Weiguo Wan, Jun Liu   +6 more
doaj   +1 more source

Peripheral retinal leakage in POEMS syndrome

International Journal of Retina and Vitreous, 2021
Background POEMS (polyneuropathy, organomegaly, endocrinopathy, myeloma protein, skin changes) syndrome is a rare blood disorder with multi-system involvement. The cause is unknown.
Andrew Rising Carey, Praveen Jeyaseelan
doaj   +1 more source

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

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   +1 more source