A case of benign immunoglobulin D monoclonal gammopathy of undetermined significance with 26 years of follow-up

被引:0
作者
Anderson, Larry D., Jr. [1 ]
Blade, Joan [2 ]
Kyle, Robert A. [3 ]
机构
[1] UT Southwestern Med Ctr, Simmons Comprehens Canc Ctr, Myeloma Waldenstroms & Amyloidosis Program, Hematol Malignancies & Cellular Therapy Program, Dallas, TX USA
[2] Univ Barcelona, Hosp Clin Barcelona, Inst Invest Biomed August Pi I Sunyer, Dept Hematol,Amyloidosis & Myeloma Unit, Barcelona, Spain
[3] Mayo Clin, Div Hematol, Rochester, MN USA
来源
EJHAEM | 2024年 / 5卷 / 01期
关键词
Immunoglobulin D (IgD); MGUS; monoclonal gammopathy; MULTIPLE-MYELOMA; SIGNIFICANCE MGUS;
D O I
10.1002/jha2.846
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The presence of a serum immunoglobulin D (IgD) monoclonal protein (M-protein) is seen in < 1% of patients with monoclonal gammopathies and is usually indicative of a malignant plasma cell disorder. Only a few cases of well-documented benign monoclonal gammopathy of undetermined significance (MGUS) of IgD subtype have been reported, and only 2 of those had over 5 years of follow-up at the time they were reported. Herein we describe longer-term follow-up of one of those 2 patients who has subsequently passed away from unrelated causes but never developed multiple myeloma or amyloidosis after 26 years of follow-up. Although IgD MGUS is extremely rare, this case confirms that presence of an IgD M-Protein is not always synonymous with a malignant plasma cell process.
引用
收藏
页码:235 / 237
页数:3
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