Nodular cutaneous amyloidosis and carpal tunnel syndrome due to the amyloidogenic transthyretin His 114 variant

被引:13
|
作者
Mochizuki, H
Kamakura, K
Masaki, T
Hirata, A
Tokuda, T
Yazaki, M
Motoyoshi, K
Ikeda, S
机构
[1] Natl Def Med Coll, Dept Internal Med 3, Tokorozawa, Saitama 3598513, Japan
[2] Shinshu Univ, Sch Med, Dept Med Neurol, Matsumoto, Nagano 3908621, Japan
来源
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS | 2001年 / 8卷 / 02期
关键词
familial amyloid polyneuropathy; amyloid; transthyretin; ATTR Tyr114His; nodular cutaneous amyloidosis;
D O I
10.3109/13506120109007352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This is the second report of transthyretin (TTR) amyloidosis in a patient who had A TTR Tyr114His diagnosed by mass spectrometry and gene analysis. This case had some clinical features that differed from those of the first reported cases. The patient, 73-year-old man, complained of generalized cutaneous tubercula that had starred at age 68. These tubercula gradually increased in size and became generalized. He felt a slight numbness in his extremities. Clinical and electrophysiological examinations revealed that he had bilateral carpal tunnel syndrome (CTS), whereas there was no clear evidence of sensory and/or motor polyneuropathy. Autonomic symptoms were not present. Biopsy studies revealed that both his tuberculum and his sural nerve contained TTR-related amyloid. In his sural nerve, amyloid deposits were observed mainly in the perineurium, not in the endoneurium, and there was no significant depletion of myelinated fibers. The features of this patient were clinically characterized by generalized cutaneous amyloid deposits and late-onset CTS with a lack of overt polyneuropathy and autonomic dysfunction. The unique clinical features in this case seemed to be consistent with the distribution of amyloid deposits.
引用
收藏
页码:105 / 110
页数:6
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