The syndrome of the supplementary motor area (SIMA) is not well recognized
and its features can easily be confused with pyramidal weakness. The author
s describe the SMA syndrome in six patients who underwent surgery for tumou
rs located in the SMA, three in the dominant and three in the non-dominant
hemispheres. All of them underwent complete resection of the anatomically d
escribed SMA, with partial (n=4) or total resection (n=2) of the tumour. In
the postoperative period, all these patients exhibited reduction of sponta
neous movements and difficulty in performing voluntary motor acts to comman
d in the contralateral limbs, although the tone in the limbs was maintained
or increased. The function of these limbs in serial automatic motor activi
ties (for example, dressing and walking) was, however, relatively unaffecte
d. Speech deficits were seen in only one of three patients with the dominan
t SMA syndrome. Besides a severe impairment of volitional movements, the sa
lient features of the deficits in this syndrome are hemineglect and dysprax
ia or apraxia involving the contralateral limbs. All patients recovered the
ir motor functions over varying periods of time ranging from one to a few w
eeks. Long-term follow-up (median 24 months) in five patients revealed comp
lete return of function in the affected limbs. It is important to recognize
the entity of the SMA syndrome and differentiate it from the deficits that
result from operative damage to the motor cortex as the deficits associate
d with the former are likely to recover almost completely over a short peri
od of time.