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2.
Acta Neurochir (Wien) ; 158(4): 663-669, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26897024

ABSTRACT

BACKGROUND: A pineal cyst is a benign affection of a pineal gland on the borderline between a pathological lesion and a variant of normality. Clinical management of patients with a pineal cyst remains controversial, especially when patients present with non-specific symptoms. METHODS: An online questionnaire consisting of 13 questions was completed by 110 neurosurgeons worldwide. Responses were entered into a database and subsequently analysed. RESULTS: Based on data from the questionnaire, the main indication criteria for pineal cyst resection are hydrocephalus (90 % of the respondents), Parinaud's syndrome (80 %) and growth of the cyst (68 %). Only 15 % of the respondents occasionally operate on patients with non-specific symptoms. If surgery is indicated, improvement is expected in 88 % of the patients. The vast majority of the respondents favour a supracerebellar infratentorial approach to the pineal region. Most (78 %) of the respondents regarded the patient registry as a potentially useful instrument. CONCLUSIONS: This survey sheds light on the current practice of pineal cyst management across the world. Most of the respondents perform surgery on pineal cysts only if patients are presenting with symptoms attributable to a mass effect. Surgery for patients with non-specific complaints (headache, vertigo) is not widely accepted, although it may prove effective. A prospective patient registry might be useful in the decision-making process in the clinical management of pineal cysts.


Subject(s)
Central Nervous System Cysts/surgery , Disease Management , Neurosurgical Procedures/methods , Pineal Gland/surgery , Practice Patterns, Physicians' , Adult , Central Nervous System Cysts/psychology , Decision Making , Female , Humans , Male , Neurosurgeons/psychology , Neurosurgical Procedures/psychology , Pineal Gland/pathology , Surveys and Questionnaires
3.
J Craniofac Surg ; 25(1): e74-6, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24406608

ABSTRACT

Reduction cranioplasty for macrocephaly improves patients' quality of life both functionally and aesthetically. However, it is indicated for only a small number of patients because of the risks of complications. Thus, it is rarely performed, and not many reports have been published. In Dandy-Walker syndrome, there is often a posterior fossa cyst continuous with the fourth ventricle. We report here a case of scaphocephalic macrocephaly because of such a cystic lesion. The patient underwent a single-stage surgery with plication of the cyst wall and posterior reduction cranioplasty. This procedure achieved good results.


Subject(s)
Central Nervous System Cysts/surgery , Craniotomy , Dandy-Walker Syndrome/surgery , Megalencephaly/surgery , Central Nervous System Cysts/diagnosis , Central Nervous System Cysts/psychology , Child, Preschool , Cranial Fossa, Posterior/pathology , Cranial Fossa, Posterior/surgery , Craniosynostoses/diagnosis , Craniosynostoses/psychology , Craniosynostoses/surgery , Craniotomy/psychology , Dandy-Walker Syndrome/diagnosis , Dandy-Walker Syndrome/psychology , Female , Follow-Up Studies , Humans , Imaging, Three-Dimensional , Magnetic Resonance Imaging , Megalencephaly/diagnosis , Megalencephaly/psychology , Postoperative Complications/diagnosis , Quality of Life/psychology , Tomography, X-Ray Computed
4.
Epilepsy Res ; 101(1-2): 185-90, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22483538

ABSTRACT

In this study, we describe three patients who each had an electroclinical overlap of two different epileptic encephalopathies (EE), with onset in a certain age period. Patient 1 had electroclinical features compatible with continuous spikes and waves during slow sleep (CSWSS) syndrome that changed into Lennox-Gastaut syndrome (LGS) (symptomatic, cause porencephalic cyst) at the age of 8.5 years. Patient 2 had LGS which evolved into CSWSS at the age of 6 years (symptomatic, cause polymicrogyria). The third patient had cryptogenic CSWSS syndrome at age the age of 7 years which evolved into LGS at the age of 7.5 years. All three patients could be considered to have two EE: CSWSS syndrome and LGS or to have had overlapping features of these epileptic syndromes.


Subject(s)
Brain Diseases/physiopathology , Electroencephalography , Epilepsy/physiopathology , Aggression/psychology , Brain Diseases/complications , Central Nervous System Cysts/complications , Central Nervous System Cysts/psychology , Child , Child, Preschool , Disease Progression , Epilepsy/etiology , Epilepsy, Rolandic/physiopathology , Epilepsy, Tonic-Clonic/physiopathology , Gait Disorders, Neurologic/etiology , Gait Disorders, Neurologic/physiopathology , Humans , Hyperkinesis/etiology , Hyperkinesis/physiopathology , Intellectual Disability/physiopathology , Learning Disabilities/etiology , Learning Disabilities/psychology , Lennox Gastaut Syndrome , Male , Malformations of Cortical Development/complications , Malformations of Cortical Development/psychology , Movement Disorders/complications , Movement Disorders/psychology , Seizures/physiopathology , Sleep/physiology , Sleep Wake Disorders/physiopathology , Spasms, Infantile/physiopathology
5.
Prenat Diagn ; 31(8): 745-9, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21484842

ABSTRACT

OBJECTIVE: To examine the effect of isolated prenatal choroid plexus cysts (CPCs) on child cognitive, behavioral, motor, and autonomic development at 18 months of age. METHODS: A prospective design was implemented to identify CPC cases and controls in mid-pregnancy. Cases (n = 25) and controls (n = 45) participated in a follow-up visit when children were 18 months of age. Child mental and motor development was assessed using standard developmental assessments, socioemotional and behavioral functioning during testing was rated by examiners, and accelerometers provided measures of motor activity and energy expenditure. Cardiac patterns were collected using a three-lead electrocardiogram (ECG) and quantified as indicators of autonomic control of the heart, including vagal tone. RESULTS: No significant differences were found in any outcome measure between children with prenatal CPC detection and those without. CONCLUSION: Findings should provide reassurance to practitioners and parents that isolated CPCs in fetuses with normal karyotypes do not affect child development after birth.


Subject(s)
Brain Diseases/congenital , Brain Diseases/diagnosis , Central Nervous System Cysts/diagnosis , Child Development , Choroid Plexus/physiopathology , Adult , Attention , Autonomic Nervous System/physiopathology , Brain Diseases/physiopathology , Brain Diseases/psychology , Case-Control Studies , Central Nervous System Cysts/physiopathology , Central Nervous System Cysts/psychology , Energy Metabolism , Female , Humans , Infant , Male , Motor Activity , Pregnancy , Prospective Studies , Psychomotor Performance , Ultrasonography, Prenatal
6.
Clin Neurol Neurosurg ; 112(6): 512-5, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20363554

ABSTRACT

We present the first case of a 57 year old man who developed severe, acute vasospasm following transcallosal resection of an unusual, xanthogranulomatous colloid cyst. The 16 year history of growth of this cyst may have resulted in its unusual pathology, and the subsequent vasospastic reaction to its excision. We discuss the potential pathological relationship between the inflammatory nature of the cyst, chemical meningitis and vasospasm, and what this implies about vasospasm in general. The severe, life-threatening vasospasm affected all four major vessels and required aggressive management by endovascular injection of nimodipine and angioplasty, with good recovery. The case illustrates a previously undescribed sequel of surgery for this condition, demonstrates an effective treatment and offers possible insights into the pathogenesis of vasospasm.


Subject(s)
Central Nervous System Cysts/surgery , Cerebral Ventricle Neoplasms/surgery , Corpus Callosum/surgery , Granuloma/surgery , Postoperative Complications/etiology , Third Ventricle/surgery , Vasospasm, Intracranial/etiology , Angioplasty , Calcium Channel Blockers/therapeutic use , Central Nervous System Cysts/pathology , Central Nervous System Cysts/psychology , Cerebral Angiography , Cerebral Ventricle Neoplasms/pathology , Cerebral Ventricle Neoplasms/psychology , Diabetes Mellitus, Type 2/complications , Granuloma/pathology , Granuloma/psychology , Humans , Magnetic Resonance Angiography , Magnetic Resonance Imaging , Male , Meningitis, Aseptic/complications , Meningitis, Aseptic/pathology , Mental Disorders/etiology , Mental Disorders/psychology , Middle Aged , Neurosurgical Procedures , Nimodipine/therapeutic use , Postoperative Complications/psychology , Tomography, X-Ray Computed , Vasospasm, Intracranial/drug therapy , Vasospasm, Intracranial/psychology
7.
J Psychosom Obstet Gynaecol ; 30(2): 95-100, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19533488

ABSTRACT

The aim of the study was to compare parents' experience of a routine ultrasound examination in the second trimester, when a choroid plexus cyst/cysts (CPC) were found (Study group; n = 22), with matched controls where no fetal deviations were identified (Control group, n = 66). All the parents had participated in a larger cohort study. The instruments used for measuring anxiety were STAI-state/trait, sense of coherence (SOC) and Parents' Expectations, Experiences, Reactions to an Ultrasound examination during pregnancy (PEER-U, State of Mind Index). Regarding the SOC and STAI-state/trait no significant differences were found between the cases and controls or within the respective group before and after the ultrasound examination. The cases had an increase in anxiety (more anxious) as measured by the instrument PEER-U after the examination, while the controls showed a significant better level of State of Mind Index (less anxious) after the examination, compared to before. Therefore PEER-U can be a more reliable instrument when studying state of mind (anxiety) in connection with ultrasound examinations, and as it is specific for this situation it does not appear to be time dependent.


Subject(s)
Anxiety/parasitology , Central Nervous System Cysts/diagnostic imaging , Central Nervous System Cysts/psychology , Choroid Plexus/diagnostic imaging , Echoencephalography/psychology , Internal-External Control , Parents/psychology , Ultrasonography, Prenatal/psychology , Adaptation, Psychological , Adult , Cohort Studies , Female , Humans , Infant, Newborn , Male , Personality Inventory/statistics & numerical data , Pregnancy , Pregnancy Trimester, Second , Psychometrics
8.
J Child Neurol ; 21(5): 419-22, 2006 May.
Article in English | MEDLINE | ID: mdl-16901449

ABSTRACT

Recently, several reports describing patients with a nonprogressive clinical course, increased signal in the cerebral white matter, and cystic changes in the anterior temporal lobes on magnetic resonance imaging (MRI) have appeared. To date, 25 patients with this very distinctive condition have been described. We report four new cases of this newly recognized entity. All have been identified primarily because of the distinctive MRI features consisting of the very unusual anterior temporal lobe cystic changes. The clinical features are characterized by severe, disabling, but nonprogressive mental and motor retardation. Magnetic resonance spectroscopy has shown increased myo-inositol and decreased N-acetylaspartate in the cerebral white matter. This is a distinctive, probably genetic, condition with characteristic neuroimaging and clinical features. In the appropriate clinical situation, the neuroimaging features are diagnostic.


Subject(s)
Brain Neoplasms/pathology , Brain Neoplasms/psychology , Central Nervous System Cysts/pathology , Central Nervous System Cysts/psychology , Temporal Lobe , Adolescent , Aspartic Acid/analogs & derivatives , Aspartic Acid/metabolism , Brain Neoplasms/metabolism , Central Nervous System Cysts/metabolism , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Inositol/metabolism , Intellectual Disability/etiology , Male , Psychomotor Disorders/etiology , Retrospective Studies
9.
J Perinatol ; 26(4): 215-23, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16554849

ABSTRACT

OBJECTIVES: To determine maternal responses to detection of a minor structural variant, the choroid plexus cyst (CPC), in their fetus on prenatal ultrasound. STUDY DESIGN: We interviewed 34 pregnant women with an isolated CPC detected on mid-pregnancy ultrasound about their objective experience at diagnosis, emotional response and subsequent reactions. Audiotaped, transcribed responses were evaluated by two independent raters and analyzed qualitatively and quantitatively. RESULTS: All women reported negative emotional responses including shock, distress, fear and decreased attachment, despite counseling by 82% of providers that the CPC was probably benign. Three women underwent amniocentesis purely for reassurance after CPC detection. Most (79%) sought information beyond what their physician provided, frequently on the internet. One half of women reported that intense negative responses were temporary. However, weeks after diagnosis, 62% continued to believe that the CPC presented some danger to their baby. CONCLUSIONS: Detection of CPC prenatally can evoke profound, negative maternal emotional responses despite accurate provider counseling. Practitioners should consider these responses when counseling parents about these and other structural variants of unclear functional significance.


Subject(s)
Attitude to Health , Central Nervous System Cysts/diagnostic imaging , Central Nervous System Cysts/psychology , Choroid Plexus/diagnostic imaging , Emotions , Mothers/psychology , Ultrasonography, Prenatal , Adaptation, Psychological , Adult , Comprehension , Culture , Fathers/psychology , Female , Follow-Up Studies , Humans , Infant, Newborn , Interview, Psychological , Male , Object Attachment , Patient Education as Topic , Physician-Patient Relations , Pregnancy , Pregnancy Trimester, Second , Ultrasonography, Prenatal/psychology
10.
J Int Neuropsychol Soc ; 11(7): 843-54, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16519263

ABSTRACT

Based on a 'Theory of Visual Attention' (TVA), whole and partial report of brief letter arrays is presented as a diagnostic tool to estimate four clinically significant attentional components: perceptual processing speed, visual working memory storage capacity, efficiency of top-down control, and spatial distribution of attention. The procedure used was short enough to be applicable within a standard clinical setting. Two brain-damaged patients, selected based on lesion location and neuropsychological test profile, were compared to a control group of 22 healthy subjects. One patient with a right inferior parietal lesion showed a pattern of non-spatially and spatially lateralized attention deficits that is typically found in neglect patients. Results from the second patient supported the decisive role of superior frontal brain structures for top-down control of visual attention. This double dissociation supports the hypothesis that, even with a short version of whole and partial report, valid and meaningful results can be obtained in the neuropsychological assessment of attention deficits. The potential and constraints of TVA-based parameter estimation for the clinical application are discussed.


Subject(s)
Attention/physiology , Central Nervous System Cysts/psychology , Frontal Lobe/pathology , Infarction, Middle Cerebral Artery/psychology , Occipital Lobe/pathology , Visual Perception/physiology , Central Nervous System Cysts/diagnostic imaging , Female , Frontal Lobe/diagnostic imaging , Functional Laterality/physiology , Humans , Infarction, Middle Cerebral Artery/diagnostic imaging , Intelligence Tests , Male , Memory, Short-Term/physiology , Middle Aged , Neuropsychological Tests , Occipital Lobe/diagnostic imaging , Tomography, X-Ray Computed
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