Neuroleptic Malignant Syndrome in Striatonigral Degeneration

1988 ◽  
Vol 153 (2) ◽  
pp. 254-255 ◽  
Author(s):  
W. R. G. Gibb

A case of probable neuroleptic malignant syndrome (NMS) complicating l-dopa withdrawal in striatonigral degeneration is described. This case suggests that the hyperthermia of NMS is due to peripheral heat production associated with severe muscular rigidity secondary to withdrawal of striatal dopamine drive, rather than being centrally mediated by the hypothalamus, which is not involved in striatonigral degeneration.

1985 ◽  
Vol 146 (3) ◽  
pp. 317-318 ◽  
Author(s):  
Dov Aizenberg ◽  
Arieh Shalev ◽  
Hanan Munitz

SummaryThe neuroleptic malignant syndrome (NMS) is an idiosyncratic reaction to neuroleptic drugs, made up of hyperthermia, muscular rigidity, disturbance of level of consciousness and autonomic dysfunction. It is potentially lethal and should be kept in mind whilst using anti-psychotic drugs; as most patients treated by them require further anti-psychotic treatment, the clinician faces the problem of treating those patients after a NMS episode, yet reports in the literature have generally neglected the problem of late management. A patient suffering from a psychosis and NMS is presented, and a rationale for management offered.


1995 ◽  
Vol 13 (3) ◽  
pp. 255-256
Author(s):  
Masayuki Itoh ◽  
Eijii Nakano ◽  
Atsushi Ieshima ◽  
Kenzo Takeshita

1992 ◽  
Vol 161 (4) ◽  
pp. 558-560 ◽  
Author(s):  
D. A. C. White

Separate episodes of both catatonia and the so-called ‘neuroleptic malignant syndrome’ (NMS) occurred within the same patient. The only evidence for NMS in this case was prior administration of a neuroleptic and the presence of generalised muscular rigidity. It is suggested that it is misleading to view these conditions as separate diagnostic entities and that NMS is probably more correctly incorporated into the catatonic disorders.


2006 ◽  
Vol 37 (S 1) ◽  
Author(s):  
JW Miller-Horn ◽  
S Kumar ◽  
T Soman ◽  
DS Khurana ◽  
A Legido ◽  
...  

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