Sensory nerve pathology in multifocal motor neuropathy

1996 ◽  
Vol 39 (3) ◽  
pp. 319-325 ◽  
Author(s):  
Andrea M. Corse ◽  
Vinay Chaudhry ◽  
Tom O. Crawford ◽  
David R. Cornblath ◽  
Ralph W. Kuncl ◽  
...  
Diagnostics ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 755
Author(s):  
Marco Luigetti ◽  
Silvia Giovannini ◽  
Angela Romano ◽  
Giulia Bisogni ◽  
Francesco Barbato ◽  
...  

Objective: Multifocal motor neuropathy (MMN) is a rare inflammatory neuropathy, clinically characterized by exclusive motor involvement. We wished to evaluate the possible presence of sensory dysfunction, including the evaluation of small fibres, after a long-term disease course. Patients and methods: seven MMN patients, regularly followed in our Neurology Department, underwent clinical evaluation, neurophysiological examination by nerve conduction studies (NCSs), and Sudoscan. We compared neurophysiological data with a group of patients with other disorders of the peripheral nervous system. Results: NCSs showed a reduction of sensory nerve action potential amplitude in 2/7 MMN patients. Sudoscan showed borderline electrochemical skin conductance (ESC) values in 3/7 MMN patients (two of them with abnormal sensory NCSs). Conclusions: Our results confirm that sensory involvement may be found in some MMN after a long-term disease course, and it could also involve the small fibres.


Author(s):  
Bashar Katirji

Multifocal motor neuropathy (MMN) is a relatively rare chronic immune-mediated neuropathy. Distinguishing MMN from motor neuron disease is essential since the disorder is amenable to treatment. This case presents a patient with MMN and multiple conduction blocks of motor nerves. It highlights the total sparing of sensory nerve conduction studies. Criteria for the diagnosis of MMN are emphasized. The importance and relevance of serum anti-glycolipid antibodies and conduction blocks in the diagnosis of MMN remains a controversial issue. The differential diagnosis often includes chronic inflammatory demyelinating polyradiculoneuropathy and Lewis-Sumner syndrome (multifocal acquired demyelinating sensory and motor neuropathy).


2019 ◽  
Vol 130 (10) ◽  
pp. e210-e211
Author(s):  
Keisuke Kido ◽  
Manabu Inoue ◽  
Yuta Terada ◽  
Toshiaki Hamano

2004 ◽  
Vol 33 (3) ◽  
pp. 237-242 ◽  
Author(s):  
Vinay Chaudhry ◽  
Andrea M. Corse ◽  
David R. Cornblath ◽  
Ralph W. Kuncl ◽  
Daniel B. Drachman ◽  
...  

2021 ◽  
Vol 101 ◽  
pp. 79-84
Author(s):  
Jeroen W. Bos ◽  
Henny G. Otten ◽  
Ingrid J.T. Herraets ◽  
H. Stephan Goedee ◽  
E.A. Cats ◽  
...  

2016 ◽  
Vol 63 (1.2) ◽  
pp. 104-107 ◽  
Author(s):  
Hiroyuki Nodera ◽  
Yuishin Izumi ◽  
Naoko Takamatsu ◽  
Ryuji Kaji

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