Mass spectrometry analysis reveals non-mutated apolipoprotein a1 lumbosacral radiculoplexus amyloidoma

作者：Loavenbruck Adam J; Chaudhry Vinay; Zeldenrust Steven R; Spinner Robert J; Theis Jason D; Klein Christopher J^*

来源：Muscle & Nerve, 2012, 46(5): 817-822.

DOI：10.1002/mus.23415

• amyloidogenesis
• amyloidoma
• apolipoprotein A1
• peripheral neuropathy
• mass spectrometry

Introduction: In rare instances, amyloidosis presents as a focal, macroscopic lesion involving peripheral neural tissues (amyloidoma). In all known reported cases, peripheral nerve amyloidomas have had immunoglobulin light-chain fibril composition and occurred in the context of paraproteinemia. Methods: A 46-year-old man presented with progressive insidious-onset right lumbosacral radiculoplexus neuropathy without paraproteinemia. MRI-targeted fascicular nerve biopsy was performed on an enlarged sciatic nerve after earlier distal fibular nerve biopsy was nondiagnostic. Laser dissected mass spectroscopy of the discovered amyloid protein was performed after immunohistochemistry failed to identify the specific amyloid protein. Complete gene sequencing of apolipoprotein A1 (ApoA1) was performed. Results: Only wild-type ApoA1 amyloid was found in the congophilic component in the nerve. Conclusions: This case highlights the utility of MRI-guided fascicular nerve biopsy combined with laser-dissected mass spectrometric analysis. Importantly, the case expands the known causes of amyloidomas to include wild-type ApoA1. Muscle Nerve 46: 817822, 2012

• 出版日期2012-11