Chiari Malformasyonları Cerrahi Tedavisinin Tarihçesi ve Güncel Yaklaşımlar
Özet
Santral sinir sisteminin kranial veya spinal kompartmanlarına bağlı nörolojik semptom ve bulguları olan Chiari malformasyonlarının (CM) tedavisinde özellikle tıbbı tedavi protokolleri yetersiz kaldığı hastalarda cerrahi tedavi seçeneklerine ihtiyaç vardır. CM’ların cerrahi tedavisinde amaç özellikle hastalığın patogenezini iyileşetirerek klinik ve radyolojik bulgu ve semptomların iyileşmesidir.
Yöntemler: Tip-0, I, 1.5 CM’ların cerrahi tedavisinde minimal invazif yaklaşımlardan araknoid korumalı duraplastili posterior fossa dekompresyonu (ADPFD) tekniği çoğu Nöroşirürji kliniklerinde yaygın sıklıkla uygulanmaktadır.
Sonuçlar: Chiairi malformasyonu cerrahi tedavi seçenekleri arasında minimal invazif ADPFD tekniği sonrası oluşturulan yeni yapay sisterna magnanın etrafında BOS dolanımının düzelmesiyle klinik ve radyolojik bulguların iyileşmesi tesbit edilmektedir. ADPFD minimal invazif tekniği Chiairi cerrahi tedavisinde uygulandığında kabül edilebilir postoperatif komplikasyon oranlarıyla birlikte nüks olguların mükerrer cerrahilerini de önlenmektedir.
Surgical treatment options are needed for Chiari malformations (CM), which have neurological symptoms and findings related to the cranial or spinal compartments of the central nervous system, especially in patients where medical treatment protocols are insufficient. The aim of surgical treatment of CMs is to improve clinical and radiological findings and symptoms by improving the pathogenesis of the disease.
Methods: Arachnoid-protected duraplasty posterior fossa decompression (ADPFD) technique, one of the minimally invasive approaches, is frequently applied in many Neurosurgery clinics in the surgical treatment of Type-0, I, 1.5 CMs.
Results: It is observed that clinical and radiological findings improve with the improvement of CSF (cerebrospinal fluid) circulation around the newly created artificial cisterna magna after the minimally invasive ADPFD technique among Chiari malformation surgical treatment options. When the ADPFD minimally invasive technique is applied in Chiari surgical treatment, it also prevents repeated surgeries of recurrent cases with acceptable postoperative complication rates.
Referanslar
Van Houweninge Graftdijk CJ: Over hydrocephalus. Eduard Ijdo, Leiden (1932).
Van Houweninge Graftdijk CJ Heelkunde voor Den Medicus Practicus. HE Stenfert's Kroese, Leiden (1940).
Russell DS, Donald C (1935) The mechanism of internal hydrocephalus in spina bifida. Brain 58:203–215.
Penfield W, Coburn DF (1938) Arnold–Chiari malformation and its operative treatment. Arch Neurol Psychiatry 40:328–336.
McConnell AA, Parker HL (1938) A deformity of the hind-brain associated with internal hydrocephalus. Its relation to the Arnold–Chiari malformation. Brain 61:415–429.
Bucy PC, Lichtenstein BW (1945) Arnold–Chiari deformity in an adult without obvious cause. J Neurosurg 2:245–250.
Chorobski J, Stepien L (1948) On the syndrome of Arnold–Chiari. Report of a case. J Neurosurg 5:495–500.
Gardner WJ, Goodall RJ. The surgical treatment of Arnold-Chiari malformation in adults; an explanation of its mechanism and importance of encephalography in diagnosis. J Neurosurg. 1950;7(3):199–206.
Gardner WJ. Hydrodynamic mechanism of syrin gomyelia: its relationship to myelocele. J Neurol Neurosurg Psychiatry. 1965;28:247–59.
Levy WJ, Mason L, Hahn JF. Chiari malformation presenting in adults: a surgical experience in 127 cases. Neurosurgery. 1983;12(4):377–90.
Logue V, Edwards M. Syringomyelia and its surgical treatment-analysis of 75 patients. J Neurol Neurosurg Psychiatry. 1981;44(4):273–84.
Klekamp J, Batzdorf U, Samii M, Bothe HW. The surgical treatment of Chiari I malformation. Acta Neurochir. 1996;138(7):788–801.
Chauvet D, Carpentier A, George B. Dura splitting decompression in Chiari type 1 malformation: clinical experience and radiological findings. Neurosurg Rev. 2009;32(4):465–70.
Durham SR, Fjeld-Olenec K. Comparison of posterior fossa decompression with and without duraplasty for the surgical treatment of Chiari malformation Type I in pediatric patients: a meta-analysis. J Neurosurg Pediatr. 2008;2(1):42–9.
Isu T, Sasaki H, Takamura H, Kobayashi N. Foramen magnum decompression with removal of the outer layer of the dura as treatment for syringomyelia occurring with Chiari I malformation. Neurosurgery. 1993;33(5):844–9; discussion 9-50.
Kotil K, Ton T, Tari R, Savas Y. Delamination technique together with longitudinal incisions for treatment of Chiari I/syringomyelia complex: a prospective clinical study. Cerebrospinal Fluid Res. 2009;6:7.
Romero FR, Pereira CAdB. Suboccipital craniectomy with or without duraplasty: what is the best choice in patients with Chiari type 1 malformation? Arq Neuropsiquiatr. 2010;68(4):623–6.
Nyland H, Krogness KG. Size of posterior fossa in Chiari type 1 malformation in adults. Acta Neurochir. 1978;40(3–4):233–42.
Cinalli G, Spennato P, Sainte-Rose C, Arnaud E, Aliberti F, Brunelle F, et al. Chiari malfor mation in craniosynostosis. Childs Nerv Syst. 2005;21(10):889–901.
Buxton N, Jaspan T, Punt J. Treatment of Chiari mal formation, syringomyelia and hydrocephalus by neu roendoscopic third ventriculostomy. Minim Invasive Neurosurg. 2002;45(4):231–4.
Decq P, Le Guerinel C, Sol JC, Brugieres P, Djindjian M, Nguyen JP. Chiari I malformation: a rare cause of noncommunicating hydrocephalus treated by third ventriculostomy. J Neurosurg. 2001;95(5):783–90.
Hayhurst C, Osman-Farah J, Das K, Mallucci C. Initial management of hydrocephalus associated with Chiari malformation Type I-syringomyelia com plex via endoscopic third ventriculostomy: an out come analysis. J Neurosurg. 2008;108(6):1211–4.
Metellus P, Dufour H, Levrier O, Grisoli F. Endoscopic third ventriculostomy for treatment of noncommunicating syringomyelia associated with a Chiari I malformation and hydrocephalus: case report and pathophysiological considerations. Neurosurgery. 2002;51(2):500–3; discussion 3-4.
Mohanty A, Suman R, Shankar SR, Satish S, Praharaj SS. Endoscopic third ventriculostomy in the man agement of Chiari I malformation and syringomy elia associated with hydrocephalus. Clin Neurol Neurosurg. 2005;108(1):87–92.
Atkinson JL, Weinshenker BG, Miller GM, Piepgras DG, Mokri B. Acquired Chiari I malformation sec ondary to spontaneous spinal cerebrospinal fluid leak age and chronic intracranial hypotension syndrome in seven cases. J Neurosurg. 1998;88(2):237–42.
Kasner SE, Rosenfeld J, Farber RE. Spontaneous intracranial hypotension: headache with a revers ible Arnold-Chiari malformation. Headache. 1995;35(9):557–9.
Mea E, Chiapparini L, Leone M, Franzini A, Messina G, Bussone G. Chronic daily headache in the adults: differential diagnosis between symptomatic Chiari I malformation and spontaneous intracranial hypoten sion. Neurol Sci. 2011;32(Suppl 3):291–4.
Puget S, Kondageski C, Wray A, Boddaert N, Roujeau T, Di Rocco F, et al. Chiari-like tonsillar herniation associated with intracranial hypotension in Marfan syndrome. Case report. J Neurosurg. 2007;106(1 Suppl):48–52.
Udayakumaran S. Post CSF shunting Chiari I mal formation--sequel or complication? Hypertension or hypotension? Childs Nerv Syst. 2009;25(11):1391–2; author reply 3.
Agostinis C, Caverni L, Montini M, Pagani G, Bonaldi G. “Spontaneous” reduction of tonsillar her niation in acromegaly: a case report. Surg Neurol. 2000;53(4):396–9.
Ammerman JM, Goel R, Polin RS. Resolution of Chiari malformation after treatment of acromegaly. Case illustration. J Neurosurg. 2006;104(6):980.
Hara M, Ichikawa K, Minemura K, Kobayashi H, Suzuki N, Sakurai A, et al. Acromegaly associated with Chiari-I malformation and polycystic ovary syn drome. Intern Med. 1996;35(10):803–7.
Lemar HJ Jr, Perloff JJ, Merenich JA. Symptomatic Chiari-I malformation in a patient with acromegaly. South Med J. 1994;87(2):284–5.
Aronson DD, Kahn RH, Canady A, Bollinger RO, Towbin R. Instability of the cervical spine after decom pression in patients who have Arnold-Chiari malfor mation. J Bone Joint Surg Am. 1991;73(6):898–906.
Fenoy AJ, Menezes AH, Fenoy KA. Craniocervical junction fusions in patients with hindbrain hernia tion and syringohydromyelia. J Neurosurg Spine. 2008;9(1):1–9.
Karnofsky D A, J. H. Burchenal J H, “The Clinical Evaluation of Chemotherapeutic Agents in Cancer,” In: C. M. MacLeod, Ed., Evaluation of Chemotherapeutic Agents, Columbia University Press, New York, 1949, P. 196.
McCormick, R. Torres, K.D. Post, B.M. Stein. Intramedullar ependymoma of the spinal cord. J Neurosurg, 72 (1990), pp. 523-532
Aliaga L, Hekman KE, Yassari R, Straus D, Luther G, Chen J, Sampat A, Frim D. A novel scoring system for assessing Chiari malformation type I treatment outcomes. Neurosurgery. 2012;70:656–65.
Sindou M, Chávez-Machuca J, Hashish H. Craniocervical decompression for Chiari type I-malformation, adding extreme lateral foramen magnum opening and expansileduroplasty with arachnoid preservation. Technique and long-term functional results in 44 consecutive adult casesecomparison with literature data. Acta Neurochir (Wien). 2002; 144:1005-1019.
Ono A, Ueyama K, Okada A, Echigoya N, Yokoyama T, Harata S. Adult scoliosis in syringomyelia associated with Chiari I malformation. Spine 2002;27:23–28.
Heiss JD, Patronas N, DeVroom HL, Shawker T, Ennis R, Kammerer W, et al. Elucidating the pathophysiology of syringomyelia. J Neurosurg. 1999;91(4):553–62
Oldfield EH, Muraszko K, Shawker TH, Patronas NJ. Pathophysiology of syringomyelia associated with Chiari I malformation of the cerebellar tonsils. Implications for diagnosis and treatment. J Neurosurg. 1994;80(1):3–15.
Vakharia VN, Guilfoyle MR, Laing RJ. Prospective study of outcome of foramen magnum decompres sions in patients with syrinx and non-syrinx associated Chiari malformations. Br J Neurosurg. 2011;26:7.
Massimi L, Frassanito P, Chieffo D, Tamburrini G, Caldarelli M. Bony decompression for Chiari malfor mation Type I: long-term follow-up. Acta Neurochir Suppl. 2019;125:119–24.
Rocque BG, George TM, Kestle J, Iskandar BJ. Treatment practices for Chiari malformation type I with syringomyelia: results of a survey of the American Society of Pediatric Neurosurgeons. J Neurosurg Pediatr. 2011;8(5):430–7.
Mutchnick IS, Janjua RM, Moeller K, Moriarty TM. Decompression of Chiari malformation with and without duraplasty: morbidity versus recurrence. J Neurosurg Pediatr. 2010;5(5):474–8.
Honeyman SI, Warr W. Posterior fossa decompression with or without duraplasty in the treatment of paediatric Chiari malformation Type I: a literature review and meta-analysis. Neurosurgery. 2019;84:E270.
Wetjen NM, Heiss JD, Oldfield EH. Time course of syringomyelia resolution following decompression of Chiari malformation Type I. J Neurosurg Pediatr. 2008;1(2):118–23.
Deng X, Yang C, Gan J, et al. Long-term outcomes after small-bone-window posterior fossa decompression and duraplasty in adults with Chiari malformation type I. World Neurosurg. 2015;84: 998-1004.
Maria Osborne-Grinter , Mohit Arora , Chandrasekaran Kaliaperumal , Pasquale Gallo. Posterior Fossa Decompression and Duraplasty with and without Arachnoid Preservation for the Treatment of Adult Chiari Malformation Type 1: A Systematic Review and Meta-Analysis World Neurosurg 2021 Jul;151:e579-e598.
Yeh DD, Koch B, Crone KR. Intraoperative ultra sonography used to determine the extent of surgery necessary during posterior fossa decompression in children with Chiari malformation type I. J Neurosurg. 2006;105(1 Suppl):26–32.
Munshi I, Frim D, Stine-Reyes R, Weir BK, Hekmatpanah J, Brown F. Effects of posterior fossa decompression with and without duraplasty on Chiari malformation-associated hydromyelia. Neurosurgery. 2000;46(6):1384–9; discussion 9-90.
Batzdorf U, McArthur DL, Bentson JR. Surgical treatment of Chiari malformation with and without syringomyelia: experience with 177 adult patients. J Neurosurg. 2013;118(2):232–42.
Jia C, Li H, Wu J, Gao K, Zhao CB, Li M, et al. Comparison decompression by duraplasty or cerebel lar tonsillectomy for Chiari malformation-I compli cated with syringomyelia. Clin Neurol Neurosurg. 2019;176:1–7.
Matsumoto T, Symon L. Surgical management of syringomyelia--current results. Surg Neurol. 1989;32(4):258–65. 69.
Hoffman CE, Souweidane MM. Cerebrospinal fluid-related complications with autologous duraplasty and arachnoid sparing in type I Chiari malformation Neurosurgery. 2008 Mar;62(3 Suppl 1):156-60;
Parker, S .R, Harris, P, Cummings,T.J., et al., Complications following decompression of Chiari malformation type I in children: dural graft or sealant?, J. Neurosurg. Pediatr. 8 (2011) 177-183.
Lee H S, Lee S H, Kim E S, et al. Surgical results of arachnoid-preserving posterior fossa decompression for Chiari I malformation with associated syringomyelia, J. Clin. Neurosci. 19 (2012) 557-560.
Pare LS, Batzdorf U. Syringomyelia persistence after Chiari decompression as a result of pseudo meningocele formation: implications for syrinx pathogenesis: report of three cases. Neurosurgery. 1998;43(4):945–8.
Pillay PK, Awad IA, Little JR, Hahn JF. Surgical man agement of syringomyelia: a five year experience in the era of magnetic resonance imaging. Neurol Res. 1991;13(1):3–9.