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Detection of MYD88 L265P in patients with lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia and other B-cell non-Hodgkin lymphomas [PDF]
BACKGROUND: Recent studies have identified a high prevalence of the MYD88 L265P mutation in lymphoplasmacytic lymphoma (LPL)/Waldenstrom macroglobulinemia (WM) cases, whereas low frequencies have been observed in other B cell non-Hodgkin lymphomas (NHLs).
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Se describe el caso clínico de un paciente de 60 años de edad, quien era atendido en su área de salud por presentar síntomas aparentemente banales y palidez cutaneomucosa.
Ana Dolores Izquierdo Calzado
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Bing–Neel syndrome (BNS) is a rare complication of Waldenstrom macroglobulinemia (WM) defined by a lymphoplasmacytic infiltration of the central nervous system (CNS). Patients present with a range of neurologic symptoms of variable severity.
Ananth Arjunan, Hema Rai
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Syncope as a presentation of Waldenstrom Macroglobulinemia
: Syncope as defined by ACC/AHA is defined as a symptom that presents with an abrupt, transient, complete loss of consciousness, associated with inability to maintain postural tone, with rapid and spontaneous recovery without clinical features of other ...
Kondapavuluru, Roy Subash +3 more
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Clinicopathologic spectrum of Waldenstrom\u27s macroglobulinemia: a single center experience.
Waldenstrom\u27s Macroglobulinemia (WM) is a B cell neoplasm characterized by infiltration of the bone marrow by a lymphoplasmacytic infiltrate and an IgM monoclonal gammopathy. We report a 15-year review of Patients diagnosed with WM at our center.
Adil, Salman +3 more
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Managing complications secondary to Waldenstrom's macroglobulinemia
Introduction: Waldenstrom's macroglobulinemia (WM) is a rare lymphoma characterized by the accumulation of IgM-secreting lymphoplasmacytic cells in the bone marrow and other organs. Clinical sequelae relate to direct tissue infiltration by malignant
Pessach, Ilias +2 more
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An Atypical Case of Relapsing Polychondritis Associated With Waldenström Macroglobulinemia
Relapsing polychondritis is a rare disease characterized by relapsing-remitting inflammation of cartilage and has been found to be associated as a paraneoplastic syndrome to hematologic malignancies.
Robin H. Lo, Bavani Nadeswaran
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