Morgan Jonathan T, Scumpia Alexander J, Webster Toni M, Mittler Mark A, Edelman Morris, Schneider Steven J
Division of Pediatric Neurosurgery, Department of Neurosurgery, Schneider Children's Hospital, North Shore-Long Island Jewish Medical Center, New Hyde Park, NY 11042, USA.
Pediatr Neurosurg. 2008;44(3):234-8. doi: 10.1159/000121382. Epub 2008 Mar 20.
Patients with pineal lesions typically present with the classical signs of increased intracranial pressure (headache, nausea, vomiting) and/or Parinaud's syndrome. Rare symptomatology of secondary parkinsonism attributed to pineal lesions has been previously reported in the literature. We describe an unusual case of a pineal cyst in a patient with the presenting sign of a resting tremor.
We report an 18-year-old Caucasian female who presented with a 1-month history of a new-onset progressive, unilateral low-frequency right-hand resting tremor with associated headache, nausea, vomiting, and excessive diarrhea. Magnetic resonance imaging demonstrated an atypical appearance with enhancement of a mildly prominent pineal gland, possibly representing a pineal cyst. The patient did not exhibit radiographic signs of hydrocephalus. Based upon the radiographic appearance, one could not exclude with absolute certainty the presence of a malignancy. The patient ultimately underwent a bilateral suboccipital craniotomy with gross total resection of the lesion. Postoperatively, the patient exhibited immediate resolution of her preoperative resting tremor and continues to be symptom free at 1 year.
A new-onset, resting tremor and/or other secondary parkinsonism symptoms should raise clinical suspicions of pineal lesions. Treatment can be guided based on tissue type and the presence or absence of hydrocephalus. We observed that complete surgical resection of the lesion provided the best treatment option for the total resolution of symptoms attributed to the disturbance of the microvasculature surrounding the nigro-striatal-pallidal system.
松果体病变患者通常表现为颅内压升高的典型症状(头痛、恶心、呕吐)和/或帕里诺德综合征。先前文献中曾报道过归因于松果体病变的继发性帕金森综合征的罕见症状。我们描述了一例以静止性震颤为主要表现的松果体囊肿的不寻常病例。
我们报告一名18岁的白种女性,她有1个月新发的进行性、单侧低频右手静止性震颤病史,伴有头痛、恶心、呕吐和严重腹泻。磁共振成像显示松果体轻度突出并强化,表现不典型,可能为松果体囊肿。患者未表现出脑积水的影像学征象。根据影像学表现,不能绝对排除恶性肿瘤的存在。患者最终接受了双侧枕下开颅手术,病变被全切。术后,患者术前的静止性震颤立即消失,1年后仍无症状。
新发的静止性震颤和/或其他继发性帕金森综合征症状应引起临床对松果体病变的怀疑。可根据组织类型以及是否存在脑积水来指导治疗。我们观察到,完全手术切除病变为完全消除因黑质-纹状体-苍白球系统周围微血管紊乱所致症状提供了最佳治疗选择。