Zobrazeno 1 - 10
of 231
pro vyhledávání: '"plasma cell disorder"'
Autor:
Camille Tessier, Richard LeBlanc, Jean Roy, Sabrina Trudel, Julie Côté, Marc Lalancette, Jean‐Samuel Boudreault, Émilie Lemieux‐Blanchard, Rayan Kaedbey, Michel Pavic
Publikováno v:
Cancer Medicine, Vol 13, Iss 17, Pp n/a-n/a (2024)
Abstract Background Plasma cell leukemia (PCL) is a rare monoclonal gammopathy, associated with short survival. Because of its very low incidence, only a few cohorts have been reported and thus, information on this disease is scarce. The goal of this
Externí odkaz:
https://doaj.org/article/41fd1e661a10445ab6a281d4f98c7702
Autor:
Xincheng Jiang, Xiaoyan Han, Fengyan Jin, Gang An, Jian Hou, Jingsong He, Qingming Wang, Wenjun Wu, Yi Zhao, Songfu Jiang, Shuchan Li, Zhenshu Xu, Gaofeng Zheng, Yang Yang, Qingxiao Chen, Donghua He, Yi Li, zhen cai
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
Objectives This study aims to assess the impact of the nationwide Omicron outbreak in December 2022 on Chinese patients with plasma cell disorders (PCD), focusing on the clinical characteristics of PCD patients with COVID-19 and the risk factors cont
Externí odkaz:
https://doaj.org/article/cee0be6236ea4ed79e0077781a0fd663
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a rare multisystemic clonal plasma cell disorder. Pulmonary involvement is frequently found in patients with POEMS syndrome,
Externí odkaz:
https://doaj.org/article/3f5bdc3b816f4b4ba6326bbb35bbe78b
Publikováno v:
Hemato, Vol 3, Iss 4, Pp 731-741 (2022)
Waldenström macroglobulinemia (WM) is a rare lymphoplasmacytic disorder characterized by an IgM paraprotein. The clinical presentation of WM varies and can include common manifestations such as anemia and hyperviscosity, in addition to less common f
Externí odkaz:
https://doaj.org/article/df053e0eb31b4eb78e97035deb58a1c0
Akademický článek
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Publikováno v:
JAAD Case Reports, Vol 25, Iss , Pp 97-99 (2022)
Externí odkaz:
https://doaj.org/article/e3561e19a4bf4eba8d4814688c8c5ad8
Autor:
Zhuo-Fan Xu, Jing Ruan, Long Chang, Sijin Wu, Jinkai Lin, Wei Wang, XinXin Cao, Lu Zhang, Jian Li, Daobin Zhou, Wei Zhang
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
The TEMPI syndrome is a novel and rare disease with five distinct clinical features: Telangiectasis, Erythrocytosis, Monoclonal gammopathy, Perinephric fluids collection, and Intrapulmonary shunting. Here, we report three cases of TEMPI syndrome and
Externí odkaz:
https://doaj.org/article/ed3eb4d5738b46cf9924e3828fbdbab8
Publikováno v:
Balneo and PRM Research Journal, Vol 14, Iss 2, p 558 (2023)
POEMS syndrome is a paraneoplastic disorder manifested by peripheral neuropathy and monoclonal plasma cell dyscrasia. Due to its clinical and electrophysiological aspect, POEMS syndrome is often mistaken as a chronic inflammatory demyelinating polyne
Externí odkaz:
https://doaj.org/article/9ae9210b9ae640b987d6f4ea3c43545d
Akademický článek
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Publikováno v:
BMC Ophthalmology, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background The purpose of this case series was to further characterize proteasome inhibitor associated chalazia and blepharitis, to investigate outcomes of different management strategies, and to propose a treatment algorithm for eyelid comp
Externí odkaz:
https://doaj.org/article/1ee1a9d5945f475d934c4080a224b66f