Late contralateral hyperhidrosis in lateral medullary infarcts

被引:29
作者
Rousseaux, M [1 ]
Hurtevent, JF [1 ]
Benaim, C [1 ]
Cassim, F [1 ]
机构
[1] CHU LILLE,SERV NEUROPHYSIOL CLIN,F-59037 LILLE,FRANCE
关键词
autonomic dysfunctions; cerebral infarction; medulla oblongata; sweating; Wallenberg's syndrome;
D O I
10.1161/01.STR.27.5.991
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose This study describes unilateral increases of sweating reactions observed in the months after contralateral medullary infarct; evaluation of sympathetic cutaneous response may help to explain sweating disorders. Summary of Report After the discovery of the clinical phenomenon in one case, patients admitted between 1990 and 1993 were systematically evaluated clinically and electrophysiologically. In a group of five patients presenting with lateral or dorsal medullary lesions, two exhibited an increase of contralateral sweating reactions that appealed 6 to 8 months after stroke, were elicited by effort and exposure to heat and stress, and were more severe over the forehead, face, and upper trunk. In one case, this was clinically associated with an absence of sweating on the side of the lesion. During the late phase after stroke, in three patients presenting with lateral medullary lesions, electrophysiological evaluation revealed significant asymmetry of the sympathetic skin response, which was higher on the side contralateral to the lesion than on the ipsilateral side. In one patient, no response could be elicited by stimulations applied on the side of the lesion. Conclusions Contralateral hyperhidrosis can be observed in the late phase after lateral medullary infarct and is likely due to lesion of the sympathetic pathway passing through the lateral medulla, which inhibits sudomotor neurons. Evaluation of sympathetic skin response may help to explain such clinical disorders.
引用
收藏
页码:991 / 995
页数:5
相关论文
共 33 条
[1]   EXCESSIVE SWEATING - AN UNCOMMON SIGN OF BASILAR ARTERY-OCCLUSION [J].
AWADA, A ;
AMMAR, A ;
ALRAJEH, S ;
BOROLLOSI, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1991, 54 (03) :277-278
[2]  
BERNTHAL PJ, 1984, NEUROPHARMACOLOGY, V23, P31, DOI 10.1016/0028-3908(84)90213-2
[3]   HOLMES-ADIE SYNDROME WITH PROGRESSIVE AUTONOMIC DEGENERATION [J].
BONNIN, M ;
WHELAN, RF ;
SKINNER, SL .
AUSTRALASIAN ANNALS OF MEDICINE, 1961, 10 (04) :304-+
[4]  
BUCY PAUL C., 1935, ARCH NEUROL AND PSYCHIATRY, V33, P30
[5]  
Caparros-Lefebvre D, 1993, Clin Auton Res, V3, P239, DOI 10.1007/BF01829012
[6]  
Carpenter MB., 1983, HUMAN NEUROANATOMY, V8th
[7]  
CURRIER RD, 1961, NEUROLOGY, V1, P778
[8]  
Currier RD, 1969, HDB CLIN NEUROLOGY, V2, P217
[9]   LOSS OF FACIAL SWEATING AND FLUSHING IN HOLMES-ADIE SYNDROME [J].
DRUMMOND, PD ;
EDIS, RH .
NEUROLOGY, 1990, 40 (05) :847-849
[10]   BILATERAL OCCLUSION OF BASILAR ARTERY BRANCHES [J].
FISHER, CM .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1977, 40 (12) :1182-1189