Diabetic and nondiabetic lumbosacral radiculoplexus neuropathies: New insights into pathophysiology and treatment

被引:191
作者
Dyck, PJB
Windebank, AJ
机构
[1] Mayo Clin, Peripheral Neuropathy Res Lab, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
关键词
diabetic amyotrophy; diabetic lumbosacral radiculoplexus neuropathy; lumbosacral plexopathy; lumbosacral radiculoplexus neuropathy; mirrovasculitis; necrotizing vasculitis; peripheral neuropathy;
D O I
10.1002/mus.10080
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Diabetic lumbosacral radiculoplexus neuropathy (DLRPN) (also called diabetic amyotrophy) is a well-recognized subacute, painful, asymmetric lower-limb neuropathy that is associated with weight loss and type II diabetes mellitus. Nondiabetic lumbosacral radiculoplexus neuropathy (LRPN) has received less attention. Comparison of large cohorts with DLRPN and LRPN demonstrated that age at onset, course, type and distribution of symptoms and impairments, laboratory findings, and outcomes are similar. Both conditions are lumbosacral radiculoplexus neuropathies that are associated with weight loss and begin focally with pain but that evolve into widespread, bilateral paralytic disorders. Although both are monophasic illnesses, patients have prolonged morbidity from pain and weakness, and many patients become wheelchair-dependent. Although motor-predominant, there is unequivocal evidence that autonomic and sensory nerves are also involved. Cutaneous nerves from patients with DLRPN and LRPN show pathological evidence of ischemic injury (multifocal fiber loss, perineurial thickening and degeneration, neovascularization, microfasciculation, and swollen axons with accumulated organelles) and microvasculitis (mural and perivascular inflammation, separation and fragmentation of mural smooth muscle layers of microvessels and hemosiderin-laden macrophages). Controlled trials with immune-modulating therapies in DLRPN are in progress, and preliminary data suggest that such therapy may be beneficial in LRPN. It is likely that DLRPN and LRPN are immune-mediated neuropathies that should be separated from chronic inflammatory demyelinating polyneuropathy and from systemic necrotizing vasculitis. (C) 2002 Wiley Periodicals, Inc.
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页码:477 / 491
页数:15
相关论文
共 50 条
[1]   THE NATURAL-HISTORY OF ACUTE PAINFUL NEUROPATHY IN DIABETES-MELLITUS [J].
ARCHER, AG ;
WATKINS, PJ ;
THOMAS, PK ;
SHARMA, AK ;
PAYAN, J .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1983, 46 (06) :491-499
[2]   PROXIMAL DIABETIC NEUROPATHY [J].
ASBURY, AK .
ANNALS OF NEUROLOGY, 1977, 2 (03) :179-180
[3]  
Auche MB, 1890, ARCH MED EXP ANAT PA, V2, P635
[4]   RELAPSING LUMBOSACRAL PLEXUS NEUROPATHY - REPORT OF 2 CASES [J].
AWERBUCH, GI ;
NIGRO, MA ;
SANDYK, R ;
LEVIN, JR .
EUROPEAN NEUROLOGY, 1991, 31 (06) :348-351
[5]   THE BRUNS-GARLAND SYNDROME (DIABETIC AMYOTROPHY) - REVISITED 100 YEARS LATER [J].
BAROHN, RJ ;
SAHENK, Z ;
WARMOLTS, JR ;
MENDELL, JR .
ARCHIVES OF NEUROLOGY, 1991, 48 (11) :1130-1135
[6]  
BASTRON JA, 1981, MAYO CLIN PROC, V56, P725
[7]   PAINFUL LUMBOSACRAL PLEXOPATHY WITH ELEVATED ERYTHROCYTE SEDIMENTATION-RATE - A TREATABLE INFLAMMATORY SYNDROME [J].
BRADLEY, WG ;
CHAD, D ;
VERGHESE, JP ;
LIU, HC ;
GOOD, P ;
GABBAI, AA ;
ADELMAN, LS .
ANNALS OF NEUROLOGY, 1984, 15 (05) :457-464
[8]  
Bruns L, 1890, BERL KLIN WOCHENSCHR, V27, P509
[9]   FEMORAL NEUROPATHY [J].
CALVERLEY, JR ;
MULDER, DW .
NEUROLOGY, 1960, 10 (11) :963-967
[10]  
Chokroverty S, 1996, MUSCLE NERVE, V19, P939, DOI 10.1002/(SICI)1097-4598(199608)19:8<939::AID-MUS1>3.3.CO