Isolated amyloidosis presenting with lumbosacral radiculoplexopathy: description of two cases and pathogenic review

被引:19
作者
Ladha, Shafeeq S.
Dyck, P. James B.
Spinner, Robert J.
Perez, Domingo G.
Zeldenrust, Steven R.
Amrami, Kimberly K.
Solomon, Alan
Klein, Christopher J.
机构
[1] Mayo Clin & Mayo Fdn, Dept Neurol, Coll Med, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Neurosurg, Coll Med, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Hematol, Coll Med, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Dept Radiol, Coll Med, Rochester, MN 55905 USA
[5] Univ Tennessee, Human Immunol & Canc Program, Knoxville, TN USA
关键词
amyloidoma; amyloidosis; lumbosacral plexopathy; MGUS; neuropathy; radiculopathy;
D O I
10.1111/j.1529-8027.2006.00107.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In this study, we present two cases of infiltrative, localized amyloidosis involving lumbosacral root and plexus, e.g., isolated amyloidomas. Rare and poorly understood amyloidomas may occur in both neurologic and non-neurologic tissues. The described cases emphasize potential for localized peripheral amyloidomas: (1) potential for associated lambda light chain lymphoplasmacytic lymphoma association; (2) e isolated amyloidosis without evidence for systemic plasma cell dyscrasia; (3) features suggestive of potential pathogenesis; and (4) discussion of treatment options including immunotherapy and resection. The limited literature and experience among other cases is described.
引用
收藏
页码:346 / 352
页数:7
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