Home Page Of Neurochirurgical Department Particular Aspects. Troubles of CSF Circulation (Hydrocephalus, hydrosyringomyelia, Meningoceles); Surgical Treatment of Epilepsy; http://www.md.ucl.ac.be/nech/
Extractions: SPECIALTIES AVAILABLE Image Guided Neurosurgery (IGNS) Previously with the MKM system of Zeiss and since 2004 with the VectorVision of BrainLab NeuroEndoscopy Deep Brain Stimulation for Abnormal Movements Cranial pathology Spinal pathology Malformative Disorders Cervical Disc Disease and Spondylosis; Lumbar IntervertebralDisc Herniation; Lumbar Spinal Stenosis and Lateral Recess Syndrome
Publikationen Kinderheilkunde 1998 Woelfle J Haverkamp F. Comment on Nogues M (1999) Repeated syncopes and extendet paediatric hydrosyringomyelia. J Neurol Neurosurg Psych 65 (5) 805. http://publ.meb.uni-bonn.de/KIN1998.HTM
Extractions: Index Publikationen (deutsch) Index Publications (english) Bezugsquellen Impressum Ahrens P Pabelick C Schledt U Behne M Zielen S (Safety axpects of bronchoalveolar lavage in risk patients in childhoodcontinuous end-expiratory pCO2 monitoring). Pneumologie 1998 Mar;52(3):157-60 Albers N Management of recombinant human growth hormone therapy at puberty. Hormone Research 49 (Suppl 2): 58-61 Albers N Management of recombinant human growth hormone therapy at puberty. Horm Res 49 (Suppl 2):58-61 Carbohydrates in human Nutrition. Report of a Joint FAO/WHO expert consultation. FAO food and nutrition paper 66, pp.1-127 Bettendorf M Albers N Bauer J Heinrich UE Linderkamp O Maser Gluth C Longitudinal evaluation of salivary cortisol levels in full-term and preterm neonates. Horm Res 50:303-308 Differential immune response to influenza and pneumococcal vaccination in immunosuppressed patients after heart transplantation. Transplantation, 1998 Nov 27;66(10):1340-7 Hagen v C Noeker M Haverkamp F Kongenitale Hypothyreose: Neuropsychologische und neuromotorische Risiken. Screening Journal 1, 6-13
Äèàãíîñòèêà è äèôôåðåíöèàëüíàÿ äèàãíîñòèê Diagnostic and differential diagnostic of hydrosyringomyelia. Kopanitsa VV. From the viewpoint of the nervous system general pathology http://www.intermag.kiev.ua/uan/bulet/num9/21.html
Extractions:  ôîðìàò³ PDF Îòîíåâðîëîãè÷åñêîå èññëåäîâàíè ñ âêëþ÷åíèåì ëàðèíãîñêîïèè è ýëåêòðîíèñòàãìîãðàôèè (ïîçâîëÿåò îïðåäåëèòü óðîâåíü è ñòåïåíü ïîðàæåíèÿ ñòâîëà ãîëîâíîãî ìîçãà, âîâëå÷åíèå ÿäåð V, VIII, IX, X ïàð ÷åðåïíûõ íåðâîâ, ãèïåðòåíçèþ). Ëàìèíýêòîìèÿ ñ ÷ðåñêîæíîé è ïðÿìîé êèñòîãðàôèåé (ïîçâîëÿåò îöåíèòü ôîðìó è âåëè÷èíó ñèðèíãîìèåëèòè÷åñêîé êèñòû è åå ñîîáùåíèå ñ IV æåëóäî÷êîì). ÊÒ è ÌÐÒ, èõ ñî÷åòàíèå ñ êîíòðàñòíûìè ìåòîäàìè èññëåäîâàíèÿ (ïíåâìîìèåëîãðàôèÿ, ïîçèòèâíàÿ ìèåëîãðàôèÿ) ïîçâîëÿþò âûÿâèòü îñíîâíûå ñòðóêòóðíûå ïàòîëîãè÷åñêèå îòêëîíåíèÿ: ãèäðîöåôàëèþ, ýêòîïèþ ìèíäàëèí ìîçæå÷êà è ñòâîëà ìîçãà, îêêëþçèþ IV æåëóäî÷êà, ïîëîñòè â ìîçãå, èõ ôîðìó, ñîîáùåíèå ïîëîñòåé ñ IV æåëóäî÷êîì, óòîëùåíèå è Íà ðàííèõ ýòàïàõ áîëåçíè âûñòóïàþò ïðåæäå âñåãî ðåãèîíàðíûå èçìåíåíèÿ íà ìèêðîöèðêóëÿòîðíîì óðîâíå, ÷òî ìîæíî âûÿâèòü, èñïîëüçóÿ âåãåòàòèâíûå òåñòû, ïðîñòûå è ðåçóëüòàòèâíûå, ýëåêòðîòåðìîìåòðèþ, òåïëîâèäåíèå, èññëåäîâàíèå æèäêèìè êðèñòàëëàìè è ìåòîäû, õàðàêòåðèçóþùèå ñîñóäèñòóþ ïðîíèöàåìîñòü. Î çàèíòåðåñîâàííîñòè áîëåå âûñîêèõ îòäåëîâ ãîëîâíîãî ìîçãà, â ÷àñòíîñòè ãèïîòàëÿìóñà, áóäóò ñâèäåòåëüñòâîâàòü äàííûå èññëåäîâàíèÿ æèðîâîãî, âîäíîãî, óãëåâîäíîãî îáìåíîâ, ñîñòîÿíèÿ ñîìàòîòðîïíîé ôóíêöèè ãèïîôèçà ñ ïðîâåäåíèåì òåñòà ñ L-ÄÎÔÀ. Ïðîâåäåíèå áèîõèìè÷åñêèõ è èììóíîëîãè÷åñêèõ èññëåäîâàíèé êðîâè è öåðåáðîñïèíàëüíîé æèäêîñòè è îöåíêà ìîðôîôóíêöèîíàëüíûõ ñâîéñòâ êëåòîê êðîâè ïîçâîëÿþò ñóäèòü î ïðîãðåäèåíòíîñòè ïðîöåññà, ãëóáèíå ìåòàáîëè÷åñêèõ ñäâèãîâ è ñòåïåíè íàðóøåíèÿ èììóííûõ ñâîéñòâ îðãàíèçìà ó áîëüíûõ ãèäðîñèðèíãîìèåëèåé [4,8].
New Publication New Publication. Title hydrosyringomyelia and its management in childhood Publisher Neurosurgery Publication Type Journal ArticlePeer Review Year 1987 Chapter http://www.mayfieldclinic.com/publications.nsf/0/F3CB538F9DA4F6A6852569D500624A2
New Publication New Publication. Title Management of hydrosyringomyelia in childhood Publisher Can J Neurol Sci Publication Type Journal ArticlePeer Review Year 1986 Chapter http://www.mayfieldclinic.com/publications.nsf/0/4BC6AF5B95E9453C852569D500624A2
Karger Publishers decompression have been advocated in the treatment of the Chiari I malformation, especially when the tonsillar herniation is associated with hydrosyringomyelia http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=
Karger Publishers External Resources 5 Isu T, Iwasaki Y, Akino M, Abe H hydrosyringomyelia associated with a Chiari I malformation in children and adolescents. http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=
Pediatrix Medical Group - Parent's Guide - Conditions & Diseases hydrosyringomyelia A split that can occur in the spinal cord Not visible to the eye; Requires MRI or CT Scan to diagnose. The http://www.pediatrix.com/parents/Neonatal_Medicine/Conditions/conditions-ntd.htm
Extractions: What is NTD? NTD includes a wide variety of malformations that usually involve the nervous system. They occur in the United States in about 1 of every 500 births. The spectrum of NTD includes: Meningocele A balloon-like, fluid-filled extension of the meninges Meningomyelocele Same as meningocele except it now includes spinal cord tissue Encephalocele Similar to meningomyelocele, except it involves the skull and brain Anencephaly One of the most serious malformations with lack of brain development Hydrosyringomyelia A split that can occur in the spinal cord The primary system involved is the nervous system, including the brain and the spinal cord. However, many other organs can be involved. Most common are:
Neurology -- Abstracts: Olson And Milstein 38 (4): 652 A 16year-old male with a 9-year history of spontaneously arrested hydrocephalus was noted to have hydrosyringomyelia and increased intracranial pressure http://www.neurology.org/cgi/content/abstract/38/4/652
Extractions: Department of Pediatrics, University of Washington, Seattle. A 16-year-old male with a 9-year history of spontaneously arrested hydrocephalus was noted to have hydrosyringomyelia and increased intracranial pressure shortly after sustaining minor head trauma. His symptoms resolved completely following ventriculoperitoneal shunt replacement. Hydrosyringomyelia may occur in the setting of long-standing, apparently arrested hydrocephalus.
Extractions: Journal of Neurological Sciences (Turkish) Table of Contents NOROL BIL D 18: 1 , 2001 http://www.med.ege.edu.tr/norolbil/2000/NBD12000.html Clinical Report SURGICAL MANAGEMENT OF SYRINGOMYELIA ASSOCIATED WITH CHIARI I MALFORMATION Efkan COLPAN, Sükrü CAGLAR, Ayse KARATAS, Zafer AYDIN, Yücel KANPOLAT, Ertekin ARASIL, Ahmet ERDOGAN, Cumhur DINCER, Nihat EGEMEN Ankara University, Medical Faculty, Department of Neurosurgery, Ankara, Turkey ABSTRACT Key-words: Chiari I malformation, Syringomyelia, Surgical management Chiari malformasyonlarý muhtemelen birbiri ile iliþkisiz dört tip arka beyin anomalisini kapsamaktadýr. Chiari I malformasyonu bilindiði gibi primer serebellar ektopi, tonsiller herniasyon ve birlikte serebellum kaudal kýsmýnýn ve/veya medulla oblangatanýn kaudale doðru yer deðiþtirmesi ve spinal kanal içerisine girmesi ile oluþmaktadýr. Spinal kordda syringomiyeli ve hidromiyeli olabilir . Bazý olgular lumboperitoneal ve lumbar ponksiyon sonrasý edinsel olarak görülebilmektedir. Chiari I malformasyonunda spinal kanalda beyin omurilik sývýsý ile dolu kavitasyonlarýn yani syringomyelinin önde gelen sebeplerindendir. Syringomyelinin oluþmasýnda deðiþik mekanizmalar öne sürülmüþtür. Serebrospinal sývýnýn akýmýnýn foramen magnumda intrakraniyal ve intraspinal subaraknoid boþluk arasýnda geçiþinin olmayýþý syringomiyeli oluþma sebepleri arasýnda sayýlmaktadýr. Chiari I malformasyonunda en sýk görülen belirtiler; suboksipital aðrý, kuvvetsizlik, duyu kusuru, ýsý duyusu kaybý, dengesizlik, diplopia v.b þeklinde sýralanabilir. Nörolojik muayenede santral kord sendromu, foramen magnum basýsý sendromu, serebellar sendroma ait bulgular gözlenir. Syringomiyelide cerrahi tedavi için çeþitli teknikler önerilmektedir.Bu çalýþmamýzda Chiari I malformasyonu ile birlikte görülen syringomiyeli olgularýnýn cerrahi tedavilerinin sonuçlarý deðerlendirilmiþtir.
Chiari I Malformation Can cause symptoms such as headache, balance problems, incontinence and memory problems. hydrosyringomyelia a fluid cavity in the spinal cord. http://tribble.missouri.edu/ns/chiari/chiariglossary.htm
Extractions: The Chiari Clinic Mission Who We Are Location ... Glossary Apnea: to stop breathing intermittently, often due to compression on the brainstem or lower cranial nerves Arachnoid: the closest membrane covering the brain, appears to resemble a spider web. There are 3 layers of covering of the brain and spinal cord- the dura, arachnoid and pia. Arachnoiditis: inflammation of the arachnoid Aspirate: inhaling fluids into the lungs. Inability to swallow properly, thereby allowing fluid into the lungs. Asymptomatic: without symptoms. Someone who has no symptoms that can be attributed to a disorder. Ataxia: inability to coordinate movement. Stumbling when walking, or inability to maintain a fluid gait when asked to walk a straight line. Atrophy: wasting away of the muscle, often due to lack of use or inability to exercise a muscle. Atrophic: changes in the muscle that create an appearance of being wasted away Basilar Invagination: the base of the skull and the first cervical vertebra dent inward, causing pressure on the brainstem or upper cervical spinal cord. Catheter: small, soft plastic tube used to drain fluid. A foley catheter is often inserted into the bladder for surgey. A shunt catheter can be inserted into a syrinx or the ventricles.
ÃÈÄÐÎÑÈÐÈÍÃÎÌÈÅËÈß (ÝÒÈÎÏÀÒÎÃÅÍÅÇ, ÊËÈÍÈÊÀ hydrosyringomyelia ETIOLOGY, PATHOGENESIS, CLINIC AND NEUROSURGICAL ASPECTS OF TREATMENT. VV Kopanitza. Summary. Today there is still http://www.umj.com.ua/arhiv/20/5.asp
Extractions: HYDROSYRINGOMYELIA: ETIOLOGY, PATHOGENESIS, CLINIC AND NEUROSURGICAL ASPECTS OF TREATMENT V.V. Kopanitza Summary. Today there is still much unclear in the origin of hydrosyringomyelia. Different conceptions exist as to its etiology and pathogenesis, and a number of suggestions are under discussion. The dysontogenetic theory dominant until the mid-century, attributed the gliosis origination and the spinal cord cavities formation to the embryonal nervous tissue developmental defects. Within the last decades, however, the new research methods came into being, making it possible to detalise the symptomatology and extend the knowledge of the pathogenesis of this severe and progressive central nervous system disease. Key words: hydrosyringomyelia, etiopathogenesis, classification, clinic, surgical treatment.
CHIARI MISVORMING - SYRINGOMYELIE 1900. Het onderscheid werd alsmaar vager 1971 Ballantine hydrosyringomyelia; 1988 Rhoton Syringomyelia syndrome. Naarmate http://users.pandora.be/zeldzame.ziekten/List.a/Acm-syr(1).htm
Extractions: Voordracht Prof Dr Frank Van Calenbergh 28 april 2001 In november 2000 heb ik gesproken over de bouw (anatomie) van hersenen en ruggenmerg en over de aanmaak en de stroming van het hersenvocht in normale toestanden. Daarbij heb ik syringomyelie en Chiari misvorming vermeld als aandoeningen waarbij deze processen gestoord zijn. Vandaag bespreek ik in detail de ziekten syringomyelie en Chiari misvorming. SYRINGOMYELIE Definitie De term omsluit een nogal brede waaier van ziekten zodanig dat er soms over verschillende zaken gesproken wordt als men het woord syringomyelie gebruikt. Hier ziet men een syrinx. Dat woord is het Grieks voor rietstengel of buis. Een syrinx is inderdaad zoals een rietstengel samengesteld uit stukken holle buis, soms met elkaar verbonden en soms met tussenschotten. Myelum is ruggenmerg. Syringomyelie is dus een buisvormige holte in het ruggenmerg.
Developmental CNS Abnormalities 2. Symptomatic Chiari. 3. hydrosyringomyelia. Spinal cord. Compression of upper segements and associated with hydrosyringomyelia (8090%). http://www.ucch.org/sections/neurosurg/NeuroReview/11-Pediatrics/SpinalDysraphis
Extractions: Definitions Spinal dysraphism . A generic term describing pathologic conditions related to improper closure of the caudal neuropore. Encompasses all conditions associated with spina bifida. Craniorachischisis . Total failure of neurulation. It is the most severe form of spinal dysraphism. There is no dorsal axial skeleton or dermal covering. Myeloschisis . Midline clefting of the spinal cord, partial or complete. Spina bifida cystica . Refers to a meningocele or meningomyelocele. Spina bifida aperta . A defect open to the environment. Neural plaque (or placode ). The dorsal neural tissue contained within the meningomyelocele.
ICP Monitors Neurosurg 28353357, 1991. Hoffman HJ. hydrosyringomyelia and its management in childhood. Neurosurg 21347-351, 1987. Muhonen MG, et al. http://www.ucch.org/sections/neurosurg/NeuroReview/11-Pediatrics/ChiariMalformat
Extractions: Chiari Malformations Definition Historical Arnold-Chiari malformation Classification of Chiari Malformations Type I Caudal displacement of cerebellar tonsils below foramen magnum. Type II Caudal displacement of the cerebellar vermis, IVth ventricle, and lower brainstem below foramen magnum, associated with myelodysplasia. Type III Caudal displacement of the cerebellum and brainstem into a high cervical meningocele. Type IV Cerebellar hypoplasia. Of questionable relation to the others. Embryology day 24 while the posterior neuropore closes 2-5 days later. As the neural tube closes, three flexures form shaping the cephalic end of the tube. First is the cephalic flexure, placing the forebrain at a right angle to the hindbrain. Then the cervical flexure forms. The pontine flexure forms last (about day 29) and is probably caused by increased growth within the rhombencephalon. Because of the pontine flexure formation, the thin roof of the rhombencephalon becomes creased transversely, and this fold is known as the plica chorioidea. It contains the choroid plexus that will come in direct contact with the ependymal lining, and ultimately correlate with the foramina of Luschka. All of the cerebellum will develop rostral to this line and come to overlie the posterior portion of the ventricular roof as a result of later explosive growth. rhombic lip . The paired cerebellar primordia are pushed upward and medially, meeting in the midline and starting their
MUMS List Of Disorders - H central spinal cord) (2); Hydronephrosis (44) *; hydrosyringomyelia ArnoldChiari (1); Hyper IGA Syndrome (2); Hyper IGE Syndrome http://www.netnet.net/mums/mum_h.htm
Table Of Contents Lee KS; Bae HG; Yun IG, 586. Abstract, hydrosyringomyelia associated with a Chiari I malformation in children and adolescents. Isu http://www.neurosurgery-online.com/toc/toc2604.html
