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AL amyloidosis mimicking a preferentially autonomic chronic Guillain-Barré syndrome
T Lingenfelser1, R P Linke, S Dette
1Medizinische Klinik, Eberhard-Karls Universität Tübingen.
Abstract:
We report a case history of a patient whose diagnosis of AL amyloidosis remained elusive until postmortem examination. Exhaustive autonomic neuropathy mimicking a chronic Guillain-Barré syndrome dominated the clinical picture. The problems in establishing the definitive diagnosis of AL amyloidosis even in the face of strong clinical evidence are discussed.