Zobrazeno 1 - 10
of 1 468
pro vyhledávání: '"waldenström macroglobulinemia"'
Autor:
Simon Østergaard, Lars Munksgaard, Torsten Holm Nielsen, Troels Hammer, Lars Møller Pedersen, Mette Ølgod Pedersen, Lise Mette Rahbek Gjerdrum
Publikováno v:
eJHaem, Vol 5, Iss 6, Pp 1269-1273 (2024)
Abstract Introduction: Extramedullary disease (EMD) is a rare manifestation of Waldenström macroglobulinemia (WM), and its clinical and prognostic implications are poorly understood. Methods: In this single‐center study, we investigated the clinic
Externí odkaz:
https://doaj.org/article/75e0ec76e86d43f5a477098c82e8c1fd
Autor:
Gilda Cennamo, Michele Rinaldi, Alessandro Severino, Laura De Fazio, Emanuele Malvone, Vincenzo Martinelli, Ciro Costagliola
Publikováno v:
Photodiagnosis and Photodynamic Therapy, Vol 50, Iss , Pp 104346- (2024)
Purpose: To evaluate the retinal vessel density (VD) with optical coherence tomography angiography (OCTA) in asymptomatic patients affected by Waldenström macroglobulinemia (WM) without hyperviscosity syndrome (HVS) and to highlight the presence of
Externí odkaz:
https://doaj.org/article/80ca46e82e5a4536b4ec09d19b3c47a4
Autor:
Piotr Jachimowski, Łukasz Ciulkiewicz, Mateusz Ziarkiewicz, Bogna Ziarkiewicz-Wróblewska, Marta Legatowicz-Koprowska, Krzysztof Jamroziak
Publikováno v:
Current Problems in Cancer: Case Reports, Vol 16, Iss , Pp 100325- (2024)
Waldenström macroglobulinemia (WM) is a rare indolent B-cell non-Hodgkin lymphoma with lymphoplasmacytic morphology, associated with immunoglobulin M (IgM) monoclonal gammopathy. The coexistence of WM and immunoglobulin light chain (AL) amyloidosis
Externí odkaz:
https://doaj.org/article/c7803c1fd78f4ee4a13ce15032fc3fd1
Autor:
Gilda Cennamo, Michele Rinaldi, Alessandro Severino, Laura De Fazio, Emanuele Malvone, Vincenzo Martinelli, Ciro Costagliola
Publikováno v:
Photodiagnosis and Photodynamic Therapy, Vol 48, Iss , Pp 104264- (2024)
Purpose: To evaluate the retinal vessel density (VD) with optical coherence tomography angiography (OCTA) in asymptomatic patients affected by Waldenström macroglobulinemia (WM) without hyperviscosity syndrome (HVS) and to highlight the presence of
Externí odkaz:
https://doaj.org/article/0aa157cf75fa48e2b0ab17019d8a1d1f
Publikováno v:
Clinical Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Key Clinical Message Bing–Neel syndrome (BNS) is a rare manifestation in individuals suffering from Waldenström macroglobulinemia (WM). Neurological signs and symptoms in this syndrome are almost difficult to be differentiated from other common ne
Externí odkaz:
https://doaj.org/article/86e6822ec5084f25933d46a2d5c645b3
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)
Waldenström macroglobulinemia (WM) is an infrequent variant of lymphoma, classified as a B-cell malignancy identified by the presence of IgM paraprotein, infiltration of clonal, small lymphoplasmacytic B cells in the bone marrow, and the MYD88 L265P
Externí odkaz:
https://doaj.org/article/83e1a80094f944cb857c8ec0a5e73d97
Publikováno v:
GMS Ophthalmology Cases, Vol 14, p Doc08 (2024)
Objective: To report a case of bilateral reversible optic neuropathy as the first sign of Waldenström macroglobulinemia (WM).Methods: Observational case report.Results: A 52-year-old man had a sudden loss of vision in the left eye. Examinations reve
Externí odkaz:
https://doaj.org/article/17ac77fd14fe4d9f9361dd6c79f5d6a7
Autor:
Vittorio Del Fabro, Uros Markovic, Sara Frazzetto, Roberta Sciortino, Claudia Bellofiore, Mary Ann Di Giorgio, Valerio Leotta, Anna Bulla, Angelo Curto Pelle, Federica Elia, Donato Mannina, Ugo Consoli, Giuseppe Mineo, Cesarina Giallongo, Alessandra Romano, Francesco Di Raimondo, Concetta Conticello
Publikováno v:
Frontiers in Hematology, Vol 3 (2024)
BackgroundWaldenström macroglobulinemia (WM) is a rare and indolent B-cell lymphoproliferative disorder with greater incidence in elderly patients where a precise algorithm of initial therapy is still not clear. Immunochemotherapy regimen consisting
Externí odkaz:
https://doaj.org/article/dec050af6ec34f2ea4f3548e908d35e3
Autor:
Nicolò Danesin, Greta Scapinello, Dorella Del Prete, Elena Naso, Tamara Berno, Andrea Visentin, Laura Bonaldi, Annalisa Martines, Roberta Bertorelle, Fabrizio Vianello, Carmela Gurrieri, Renato Zambello, Chiara Castellani, Marny Fedrigo, Stefania Rizzo, Annalisa Angelini, Livio Trentin, Francesco Piazza
Publikováno v:
Cancer Reports, Vol 7, Iss 4, Pp n/a-n/a (2024)
Abstract Background Renal injury related to Waldenström macroglobulinemia (WM) occurs in approximately 3% of patients. Kidney biopsy is crucial to discriminate between distinct histopathological entities such as glomerular (amyloidotic and non‐amy
Externí odkaz:
https://doaj.org/article/9af98db38b974f8aaa015cea7c106637
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Systemic amyloidosis is a rare protein misfolding and deposition disorder leading to progressive organ failure. Waldenström macroglobulinemia (WM) with systemic amyloidosis as the main manifestation is even rarer. The patient in this study presented
Externí odkaz:
https://doaj.org/article/dc377f14970e43648bac99f7c5fe0250