IgM Multiple Myeloma: A Rare Clinical Entity and Diagnostic Dilemma

Keerthy Joseph, DO, A. Greidinger, Marjan Koch, E. Behling, T. Budak-Alpdogan
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引用次数: 0

Abstract

IgM multiple myeloma is a rare disease that shares many common features with Waldenström macroglobulinemia and lymphoplasmacytic lymphoma. It has been described in the literature as having unique diagnostic findings that separate it from the more common IgG and IgA myelomas. It is important for physicians to be able to differentiate between IgM multiple myeloma, Waldenström macroglobulinemia and lymphoplasmacytic lymphoma as their treatments vastly differ. This case report describes the clinical presentation of a patient with IgM lambda multiple myeloma and highlights the pathologic and clinical findings that are specific to this rare entity. We aim to provide further evidence for the previously reported diagnostic criteria for IgM multiple myeloma.
IgM多发性骨髓瘤:一种罕见的临床实体和诊断难题
IgM多发性骨髓瘤是一种罕见的疾病,与Waldenström巨球蛋白血症和淋巴浆细胞淋巴瘤有许多共同特征。在文献中,它被描述为具有独特的诊断结果,将其与更常见的IgG和IgA骨髓瘤区分开来。对于医生来说,能够区分IgM多发性骨髓瘤、Waldenström巨球蛋白血症和淋巴浆细胞淋巴瘤是很重要的,因为它们的治疗方法有很大不同。本病例报告描述了一名IgMλ多发性骨髓瘤患者的临床表现,并强调了这种罕见实体特有的病理和临床发现。我们的目的是为先前报道的IgM多发性骨髓瘤的诊断标准提供进一步的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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