TY - JOUR
T1 - Neuromuscular Complications of Systemic Amyloidosis
AU - Namiranian, Dina
AU - Geisler, Stefanie
N1 - Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/4
Y1 - 2022/4
N2 - Systemic amyloidosis is characterized by extracellular deposition of insoluble fibrillar proteins in multiple tissues, frequently at a distance from the site of synthesis. The 2 most common forms, light chain (AL) and transthyretin (ATTR) amyloidosis can cause peripheral neuropathy and, rarely, myopathy. Diagnosis can be challenging, and abundant suspicion is required to identify patients. As neurological manifestations of amyloidosis may precede involvement of other organs by several years, recognizing amyloid neuropathy and myopathy are crucial, especially in this new and exciting era of effective therapies for AL and ATTR neuropathy. This review will focus on the neuromuscular manifestations of AL and ATTR amyloidosis, diagnostic approaches, and recent advances in the treatment of amyloid neuropathy.
AB - Systemic amyloidosis is characterized by extracellular deposition of insoluble fibrillar proteins in multiple tissues, frequently at a distance from the site of synthesis. The 2 most common forms, light chain (AL) and transthyretin (ATTR) amyloidosis can cause peripheral neuropathy and, rarely, myopathy. Diagnosis can be challenging, and abundant suspicion is required to identify patients. As neurological manifestations of amyloidosis may precede involvement of other organs by several years, recognizing amyloid neuropathy and myopathy are crucial, especially in this new and exciting era of effective therapies for AL and ATTR neuropathy. This review will focus on the neuromuscular manifestations of AL and ATTR amyloidosis, diagnostic approaches, and recent advances in the treatment of amyloid neuropathy.
KW - Familial amyloid peripheral neuropathy
KW - Light-chain
KW - Myopathy
KW - Transthyretin
UR - http://www.scopus.com/inward/record.url?scp=85129995683&partnerID=8YFLogxK
U2 - 10.1016/j.amjmed.2022.01.006
DO - 10.1016/j.amjmed.2022.01.006
M3 - Article
C2 - 35104443
AN - SCOPUS:85129995683
SN - 0002-9343
VL - 135
SP - S13-S19
JO - American Journal of Medicine
JF - American Journal of Medicine
ER -