AH amyloidosis associated with lymphoplasmacytic lymphoma secreting a monoclonal γ heavy chain carrying an unusual truncated D segment

被引:12
|
作者
Gono, Takahisa
Yazaki, Masahide [1 ]
Fushimi, Tomohisa
Suzuki, Takefumi
Uehara, Tsuyoshi
Sano, Kenji
Kametani, Fuyuki
Ito, Nobuo
Matsushita, Masahiro
Nakamura, Shigeo
Hoshii, Yoshinobu
Matsuda, Masayuki
Ikeda, Shu-ichi
机构
[1] Shinshu Univ, Sch Med, Dept Med 3, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Lab Med, Matsumoto, Nagano 3908621, Japan
[3] Tokyo Metropolitan Org Med Res, Dept Mol Neurobiol, Tokyo, Japan
[4] Iida Municipal Hosp, Dept Pathol, Iida, Japan
[5] Iida Municipal Hosp, Dept Nephrol, Iida, Japan
[6] Nagoya Univ, Sch Med, Dept Pathol, Nagoya, Aichi 466, Japan
[7] Yamaguchi Univ, Sch Med, Dept Pathol, Ube, Yamaguchi 755, Japan
关键词
AH amyloidosis; lymphoproliferative disorder; nephrotic syndrome; variable region of immunoglobulin heavy chain; short diversity (D) segment;
D O I
10.1053/j.ajkd.2006.02.174
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
To date, the presence of amyloidosis associated with immunoglobulin heavy chain (AH amyloidosis) was reported in only 7 cases. Although AH amyloidosis is caused mainly by plasma cell dyscrasia, as in AL amyloidosis, we report a 61-year-old patient who presented with nephrotic syndrome caused by AH amyloidosis associated with lymphoplasmacytic lymphoma. Biochemical and molecular analyses of the deposited amyloid fibrils and heavy-chain genes of lymphocytes showed that proliferative lymphoma cells produced a gamma heavy chain, not a mu heavy chain, which carried an unusual truncated diversity (D) segment of the variable region. Our results indicate that production of the abnormal heavy chain caused by the partially deleted D segment gene is responsible for gamma heavy-chain-related amyloid fibril formation in this patient.
引用
收藏
页码:908 / 914
页数:7
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