TY - JOUR
T1 - Multifocal radiculoneuropathy during ipilimumab treatment of melanoma
AU - Manousakis, Georgios
AU - Koch, James
AU - Sommerville, R. Brian
AU - El-Dokla, Ahmed
AU - Harms, Matthew B.
AU - Al-Lozi, Muhammad T.
AU - Schmidt, Robert E.
AU - Pestronk, Alan
PY - 2013/9
Y1 - 2013/9
N2 - Introduction: Ipilimumab, a monoclonal anti-CTLA-4 antibody, is used to treat melanoma. Neuromuscular side effects, possibly autoimmune, may occur. Methods: In this investigation we undertook a retrospective review of patient records. Results: After 3 doses of ipilimumab, a 31-year-old man developed asymmetric, severe weakness involving all limbs, respiration, and cranial nerves, which was progressive over 2 weeks. EMG/NCS showed an axonal polyradiculoneuropathy with multifocal motor conduction blocks. CSF protein was 749 mg/dl. Nerve pathology showed inflammation around the endoneurial microvessels and subperineurial edema and inflammation. Spine MRI showed leptomeningeal and anterior and posterior root enhancement. Strength improved slowly over months after ipilimumab discontinuation and immunomodulating treatment. Conclusions: Ipilimumab toxicity presented as a monophasic, multifocal, asymmetric polyradiculoneuropathy involving roots and peripheral and cranial nerves. Ipilimumab may produce a polyradiculoneuropathy with disruption of the blood-nerve barrier due to a microvasculopathy.
AB - Introduction: Ipilimumab, a monoclonal anti-CTLA-4 antibody, is used to treat melanoma. Neuromuscular side effects, possibly autoimmune, may occur. Methods: In this investigation we undertook a retrospective review of patient records. Results: After 3 doses of ipilimumab, a 31-year-old man developed asymmetric, severe weakness involving all limbs, respiration, and cranial nerves, which was progressive over 2 weeks. EMG/NCS showed an axonal polyradiculoneuropathy with multifocal motor conduction blocks. CSF protein was 749 mg/dl. Nerve pathology showed inflammation around the endoneurial microvessels and subperineurial edema and inflammation. Spine MRI showed leptomeningeal and anterior and posterior root enhancement. Strength improved slowly over months after ipilimumab discontinuation and immunomodulating treatment. Conclusions: Ipilimumab toxicity presented as a monophasic, multifocal, asymmetric polyradiculoneuropathy involving roots and peripheral and cranial nerves. Ipilimumab may produce a polyradiculoneuropathy with disruption of the blood-nerve barrier due to a microvasculopathy.
KW - Immune neuropathy
KW - Ipilimumab
KW - Peripheral nervous system vasculitis
KW - Polyradiculopathy
KW - Toxic neuropathy
UR - http://www.scopus.com/inward/record.url?scp=84883053806&partnerID=8YFLogxK
U2 - 10.1002/mus.23830
DO - 10.1002/mus.23830
M3 - Article
C2 - 23447136
AN - SCOPUS:84883053806
SN - 0148-639X
VL - 48
SP - 440
EP - 444
JO - Muscle and Nerve
JF - Muscle and Nerve
IS - 3
ER -