Camptocormia or Pisa syndrome in multiple system atrophy

被引:29
作者
Slawek, Jaroslaw
Derejko, Miroslawa
Lass, Piotr
Dubaniewicz, Miroslawa
机构
[1] Med Univ, Dept Neurosurg, Div Funct Neurosurg & Movement Disorders, PL-80211 Gdansk, Poland
[2] Inst Psychiat & Neurol, Dept Neuroelectrophysiol, PL-02957 Warsaw, Poland
[3] Med Univ, Dept Radiol, PL-80211 Gdansk, Poland
[4] Med Univ, Dept Nucl Med, PL-80211 Gdansk, Poland
关键词
camptocormia; dystonia; Parkinson's disease; multiple system atrophy; Pisa syndrome;
D O I
10.1016/j.clineuro.2005.07.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Although a mild stooped posture is a hallmark of parkinsonism, extreme trunk forward flexion is not common. This phenomenon was described in different etiological entities and called camptocormia. Other similar presentations called Pisa syndrome and antecollis were described mainly in extrapyramidal disorders. Authors present two cases of probable multiple system atrophy (MSA) with predominant parkinsonism and Pisa syndrome (or camptocormia). Both of them were previously misdiagnosed as idiopathic Parkinson's disease (PD) and one was reported I year earlier. The typical clinical presentation fulfilling the diagnostic criteria for multiple system atrophy, rapid progression with lack of responsiveness to L-DOPA and apomorphine and typical MRI putaminal pathology observed in both cases allowed us to make a diagnosis. Accuracy of clinical diagnosis in multiple system atrophy is still very poor. Therefore, unusual or rare clinical presentations may support the final diagnosis. The camptocormia, Pisa syndrome and antecollis may represent the continuum of the same motor phenomenon and most of the authors refer them to unusual form of axial dystonia. According to many clinical presentations on different forms of camptocormia/Pisa syndrome authors conclude that not etiology, but the localization of specific lesion, probably within putamen is responsible for that form of dystonia. In cases of parkinsonism and severe forward flexion of trunk multiple system atrophy, diagnosis should be considered. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:699 / 704
页数:6
相关论文
共 36 条
[1]   SOME SPECIFIC CLINICAL-FEATURES DIFFERENTIATE MULTIPLE SYSTEM ATROPHY (STRIATONIGRAL VARIETY) FROM PARKINSONS-DISEASE [J].
COLOSIMO, C ;
ALBANES, A ;
HUGHES, AJ ;
DEBRUIN, VMS ;
LEES, AJ .
ARCHIVES OF NEUROLOGY, 1995, 52 (03) :294-298
[2]   Pisa syndrome in a patient with multiple system atrophy [J].
Colosimo, C .
MOVEMENT DISORDERS, 1998, 13 (03) :607-609
[3]  
Defer GL, 1999, MOVEMENT DISORD, V14, P572, DOI 10.1002/1531-8257(199907)14:4<572::AID-MDS1005>3.0.CO
[4]  
2-C
[5]  
Djaldetti R, 1999, MOVEMENT DISORD, V14, P443, DOI 10.1002/1531-8257(199905)14:3<443::AID-MDS1009>3.0.CO
[6]  
2-G
[7]   Episodic camptocormia in PD [J].
Friedman, JH .
MOVEMENT DISORDERS, 2001, 16 (06) :1201-1201
[8]   Marked asymmetry of putaminal pathology in an MSA-P patient with Pisa syndrome [J].
Hozumi, I ;
Piao, YS ;
Inuzuka, T ;
Matsuyama, Z ;
Yamada, Y ;
Hara, A ;
Hirose, T ;
Tsuchiya, K ;
Takahashi, H .
MOVEMENT DISORDERS, 2004, 19 (04) :470-472
[9]   ACCURACY OF CLINICAL-DIAGNOSIS OF IDIOPATHIC PARKINSONS-DISEASE - A CLINICOPATHOLOGICAL STUDY OF 100 CASES [J].
HUGHES, AJ ;
DANIEL, SE ;
KILFORD, L ;
LEES, AJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (03) :181-184
[10]   Camptocormia, axial dystonia, and parkinsonism:: Phenotypic heterogeneity of a parkin mutation [J].
Inzelberg, R ;
Hattori, N ;
Nisipeanu, P ;
Mouch, SA ;
Blumen, SC ;
Carasso, RL ;
Mizuno, Y .
NEUROLOGY, 2003, 60 (08) :1393-1394