淋巴浆细胞淋巴瘤
华登氏巨球蛋白血症
边缘地带
骨髓
巨球蛋白血症
病理
医学
淋巴瘤
脾边缘带淋巴瘤
多发性骨髓瘤
内科学
免疫学
抗体
B细胞
作者
Karima Amaador,Josephine M.I. Vos,Steven T. Pals,Willem Kraan,Johan A. Dobber,Monique C. Minnema,Harry R. Koene,Peter C. de Bruin,Aeilko H. Zwinderman,Marie José Kersten
标识
DOI:10.1080/10428194.2021.2018584
摘要
Discrimination between Waldenström macroglobulinemia (WM) and marginal zone lymphoma (MZL) of the bone marrow (BM) can be difficult due to overlap in clinical, histopathologic, and immunophenotypic characteristics. We determined which characteristics can aid in the differential diagnosis of 'gray zone' cases. We compared clinical, histopathologic, immunophenotypic, and molecular features of 222 WM and 65 MZL patients. LASSO regression was employed for variable selection. The most distinguishing clinical features of WM compared to MZL were the presence of the B-symptom weight loss and IgM paraprotein. Histopathological findings were plasmacytoid differentiation, monoclonal plasma cells, and increased mast cells in the BM. Regarding flow cytometry, only CD10 and CD38 were distinguishing markers. Finally, as the expected presence of the MYD88L265P mutation showed to be of great value in the distinction between WM and MZL. Despite the great overlap, WM can often be distinguished from MZL by using a combination of characteristics. These characteristics should be weighed in complex, 'gray zone' cases.
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