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瓦尔登斯特伦巨球蛋白血症综述。

A review of Waldenstrom's macroglobulinemia.

作者信息

McDermott M K, Bell E M

机构信息

United Hospital, St. Paul, MN, USA.

出版信息

Clin J Oncol Nurs. 1999 Jul;3(3):107-11.

Abstract

Waldenstrom's macroglobulinemia (WM) is an uncommon B cell malignancy that resembles other B cell malignancies, such as multiple myeloma and chronic lymphocytic leukemia. WM's clinical course varies widely, with survival ranging from 1-16 years. WM is diagnosed when a bone marrow biopsy reveals malignant B-lymphocytes arrested at the plasmacytoid lymphocytic stage of the maturation process and when high levels of IgM are found in the serum blood. Common clinical features include anemia, abnormal bleeding, and hyperviscosity, and 20%-40% of patients present with lymphadenopathy or splenomegaly. Alkylating agents have been the most common chemotherapy agents used to treat WM. However, nucleoside analogues are being used more frequently with promising results. Nursing care includes educating the patient about the disease trajectory, providing symptom management, and monitoring the patient's response to treatment.

摘要

华氏巨球蛋白血症(WM)是一种罕见的B细胞恶性肿瘤,与其他B细胞恶性肿瘤相似,如多发性骨髓瘤和慢性淋巴细胞白血病。WM的临床病程差异很大,生存期从1年到16年不等。当骨髓活检显示恶性B淋巴细胞停滞在成熟过程的浆细胞样淋巴细胞阶段,且血清中发现高水平的IgM时,即可诊断为WM。常见的临床特征包括贫血、异常出血和血液黏稠度增加,20%至40%的患者出现淋巴结病或脾肿大。烷化剂一直是治疗WM最常用的化疗药物。然而,核苷类似物的使用越来越频繁,效果令人满意。护理工作包括向患者介绍疾病发展过程、提供症状管理以及监测患者对治疗的反应。

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