632 CLINICAL/SCIENTIFIC NOTES position-dependent levitation of the dominant arm that increased by tactile stimulation. Position-Dependent Levitation of the Dominant Arm After Left Parietal Stroke: An Unreported Feature of Posterior Alien Limb Syndrome? F.A.A. Gondim, MD, MSc, PhD,1,2,4 G.R. Oliveira, MD,3 and S. Cruz-Flores, MD4* 1 Departamento de Fisiologia e Farmacologia, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil 2 Department of Neurology, Weill Medical College of Cornell University, New York, New York, USA 3 Department of Neurology, Albert Einstein School of Medicine, Bronx, New York, USA 4 Souers Stroke Institute, Department of Neurology, Saint Louis University Hospital, St. Louis, Missouri, USA Abstract: We describe a patient with an unreported feature of posterior alien limb phenomenon characterized by positiondependent levitation of the dominant arm exacerbated by tactile stimulation and associated with low-amplitude tremor of the fingers of the right hand in addition to a sensation of strangeness in the arm, secondary to a left parietal stroke. © 2005 Movement Disorder Society Key words: alien hand phenomenon; arm levitation; parietal lobe ischemic stroke Goldstein first reported alien hand symptoms in 1908, in a patient who perceived her left hand as having a will of its own.1 The condition gained more attention when Brion and Jedynak2 described the denial of hand ownership and inability of interhemispheric exchange in patients with corpus callosum tumors. Alien hand syndrome (AHS) is defined as a combination of observable involuntary motor activity and feeling of strangeness or foreignness of one limb. Two AHS subtypes have been described classically: one secondary to callosal and the other to frontal lesions.3 An uncommon posterior variant was reported more recently resulting from lesions in the nondominant hemisphere caused by stroke or corticobasal ganglionic degeneration.3–5 Sustained, nonpurposeful, nonconflictive movements characterize this variant and include arm levitation and finger writhing.3– 6 We describe a patient with posterior AHS secondary to a left parietal lobe infarct with a previously unreported feature: a This article includes Supplementary Video, available online at http:// interscience.wiley.com/jpages/0885-3185/suppmat. *Correspondence to: Dr. Salvador Cruz-Flores, Department of Neurology, SLUH, 3635 Vista Avenue at Grand Blvd., St. Louis, MO 63110. E-mail: SALVADOR.Cruz-flores@tenethealth.com Received 12 April 2004; Revised 25 August 2004; Accepted 21 September 2004 Published online 23 February 2005 in Wiley InterScience (www. interscience.wiley.com). DOI: 10.1002/mds.20404 Movement Disorders, Vol. 20, No. 5, 2005 Case Report A 63-year-old, right-handed woman with history of smoking presented with right hemiparesis and dysarthria of sudden onset. A computed tomography (CT) scan of the head documented an ischemic stroke in the territory of the left middle cerebral artery. She was found to have 60% stenosis of the left carotid artery with ulceration. During her recovery, her hemiparesis worsened and an urgent left carotid endarterectomy was carried out. Her hemiparesis improved after few months but she had residual paresthesias in the right upper extremity. She subsequently noticed a sense of “strangeness” and some involuntary movements in the right arm associated with the paresthesias. A brain magnetic resonance imaging (MRI) revealed scattered infarcts involving the highest portions of the left parietal lobe, with minimal frontal extension and corpus callosum sparing (Fig. 1). Her neurological exam demonstrated fluent speech with normal comprehension, repetition, and naming. Her cognitive function was normal. She had no frontal release signs (grasping or palmomental reflex), right-to-left disorientation, intermanual conflict, gait, or limb apraxia. Cranial nerves were normal. She had a right upper extremity paresis (proximally 5-/5 and distally 3/5). Her reflexes were brisk and her tone was increased mildly in the right limbs. Plantar response was flexor bilaterally. She also had mild dysmetria in the right upper extremity. Pinprick, vibration, and proprioception were decreased in the right upper extremity. She demonstrated a slow levitation of her right upper extremity while in supination that was increased significantly by gentle pressure over the biceps tendon. Slow, low-amplitude tremor involving the fingers of the right hand was also noted during the arm levitation (see Video). Movements were decreased by assuming the pronator position but were not stopped by distraction or during performance of simultaneous complex movements involving multiple limbs. No exploratory or self-mutilating behavior was reported. The patient was perplexed but not angered or frightened by the movements. Discussion Our patient exhibited a constellation of symptoms consistent with the posterior variant of AHS. Similar to a recently published case,5 she had involuntary movements consisting of arm levitation. The exploratory behavior or compulsive manipulation of objects that are common in patients with frontal alien hand phenomenon were not present. She did not exhibit intermanual conflict but had a feeling of strangeness or foreignness of her right arm, which combined with her involuntary movements, points to the diagnosis of alien limb phenomenon.7 Her involuntary movements consisted mainly of right arm levitation and mild slow, low-amplitude tremor of the right fingers (see Video). To the best of our knowledge, her pattern of arm levitation was significantly different from previous cases, firstly because her levitation was position-dependent as it was obvious in supina- CLINICAL/SCIENTIFIC NOTES 633 FIG. 1. Fluid attenuated inversion recovery (FLAIR) MRI carried out after left carotid endarterectomy. Depicts a predominant high left parietal infarct with minimal left frontal lobe involvement. tion but absent in pronation. Secondly, her levitation was enhanced markedly by gentle finger pressure over the biceps tendon, suggesting facilitation by proprioceptive stimulation. Moreover, the movements were not stopped by distraction, because they were present during the simultaneous performance of multiple complex commands. Interestingly, when we asked the patient to counteract the levitation movements, she was not able to unless she voluntary moved her arm to the original supine position after significant effort. AHS encompasses a diverse combination of symptoms. Currently there is some disagreement about the requirement of “denial of ownership” in the diagnostic criteria, because isolated arm levitation was described recently in patients with progressive supranuclear palsy.8 Arm levitation is also part of the parietal motor syndrome characterized by slow levitation or sideward deviation of the forearm when patients are asked to keep both arms extended forward.9 Sensory AHS was described in about 25% of these patients.9 The etiology of the involuntary movements in the posterior AHS is not clear. A distortion of body schema secondary to an abnormal cortico-striato-thalamic circuit was proposed as the explanation although the precise neuroanatomical circuitry is yet to be understood.3,4 In our patient the clinical and MRI findings supported the diagnosis of posterior AHS resulting from a lesion of the left parietal lobe without the thalamic involvement observed in most reported cases. In light of this case, it seems that the posterior AHS variant is not restricted to nondominant parietal lesions. In summary, we report a case of posterior alien limb syndrome secondary to a left parietal infarct with features not reported previously including a position-dependent, pressure-evoked levitation of the dominant arm. Legend to the Video Position-dependent right arm levitation is demonstrated during performance of neurological examination. When the right arm is in supination, slow arm levitation is observed and is associated with tremor of the righthand fingers. Gentle pressure over the right biceps tendon accelerates arm levitation and pronation of the arm abolishes the movement. Distraction by talking or performance of complex tasks involving the other limbs does not interfere with arm levitation. Arm levitation cannot be slowed, but only stopped abruptly by opposing strong volitional movements. References 1. Goldstein K. Zur Lehre der motorischen Apraxie. Journal fur Psychologie und Neurologie 1908;11:169 –187. 2. Brion S, Jedynak CP. Troubles du transfert interhemispherique. A propos de trois observations de tumeurs du corps calleux. Le signe de la main étrangère. Rev Neurol (Paris)1972;126:257–266. 3. Scepkowski LA, Cronin-Golomb A. The alien hand: cases, categorizations, and anatomical correlates. Behav Cogn Neurosci Rev 2003;2:261–277. 4. Ay H, Buonanno FS, Price BH, Le DA, Koroshetz WJ. Sensory alien hand syndrome: case report and review of the literature. J Neurol Neurosurg Psychiatry 1998;65:306 –369. 5. Bundick T Jr, Spinella M. Subjective experience, involuntary movement, and posterior alien hand syndrome. J Neurol Neurosurg Psychiatry 2000;68:83– 85. 6. Carrilho PEM, Caramelli P, Cardoso F, Barbosa ER, Buchpiguel CA, Nitrini R. Involuntary hand levitation associated with parietal damage: another alien hand syndrome. Arq Neuropsiquiatr 2001; 59:521–525. 7. Doody RS, Jankovic J. The alien hand and related signs. J Neurol Neurosurg Psychiatry 1992;55:806 – 810. 8. Barclay CL, Bergeron C, Lang AE. Arm levitation in progressive supranuclear palsy. Neurology 1999;52:879 – 882. 9. Ghika J, Ghika-Schmid F, Bogousslasvky. Parietal motor syndrome: a clinical description in 32 patients in the acute phase of pure parietal strokes studied prospectively. Clin Neurol Neurosurg 1998; 100:271–282. Movement Disorders, Vol. 20, No. 5, 2005