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Differentiated method in surgical revascularization of the brain for the treatment of pediatric patients with moyamoya angiopathy

https://doi.org/10.17650/1683-3295-2020-22-4-28-42

Abstract

The study objective is to study the results of the differentiated method of surgical revascularization of the brain for the treatment of pediatric patients with moyamoya angiopathy.

Materials and methods. Twelve surgical interventions were performed on 12 hemispheres in 8 patients (4 male, 4 female) with moyamoya angiopathy from December 2015 to March 2020. The age of patients ranged from 6 months to 14 years old, the average age is 8 years old. To clarify the clinical course of the disease the Y. Matsushima classification was used: type I (n = 3), type III (n = 2), type IV (n = 2) and type V (n = 1) of Y. Matsushima. Stages of the disease are classified according to J. Suzuki: stage III was revealed in 5 patients, stage IV— in 3. Cerebral angiography, magnetic resonance imaging of the brain and vessels were performed; computed tomography perfusion of the brain was made in every patient. Encephaloduroarteriomyosynangiosis was used in 2 hemispheres. Extra-intracranial bypass and encephaloduro-myosynangiosis in 1; extracranial-intracranial bypass and encephaloduroarteriomyosynangiosis — in 2; extracranial-intracranial bypass and encephaloduromyoperiosteosynangiosis in 5 hemispheres; double-barreled bypass and encephaloduromyosynangiosis — in 1 hemisphere; double-barreled bypass and encephaloduromyoperiosteosynangiosis — in 1 hemisphere. In the follow-up period (6—36 months) neurological status testing, digital subtraction angiography (6 vascular territories), magnetic resonance imaging of the brain and vessels and computed tomography perfusion of the brain were performed.

Results. All patients in the follow-up period had no clinically significant ischemic events on the side of surgical intervention; there was an increase in the perfusion of the brain in comparison with preoperational values. In 1 case, transient ischemic attack occurred on the nonoperated hemisphere that did not recur after surgery. There was a regression of symptoms among children with initial neurological deficits. The angiographic result, in accordance with the method suggested by Y. Matsushima, was excellent (A group) and good (B group), except the case of moyamoya syndrome and case after indirect revascularization in zone of brain atrophy. Based on our experience, we have determined the optimal method of suturing the wound with a good cosmetic effect.

Conclusion. We can assume, that differentiated method in surgical treatment of pediatric patients with moyamoya angiopathy is highly effective for the prevention of ischemic stroke, and also has good clinic, angiographic and cosmetic result. With suitable arterial sizes, combined revascularization showed better results than indirect, especially in the clinically significant hemisphere.

About the Authors

K. S. Ovsiannikov
Federal Neurosurgical Center (Novosibirsk), Ministry of Health of Russia
Russian Federation

132/ 1 Nemirovicha-Danchenko St., Novosibirsk 630087



A. V. Dubovoy
Federal Neurosurgical Center (Novosibirsk), Ministry of Health of Russia
Russian Federation

132/ 1 Nemirovicha-Danchenko St., Novosibirsk 630087



D. A. Rzaev
Federal Neurosurgical Center (Novosibirsk), Ministry of Health of Russia
Russian Federation

132/ 1 Nemirovicha-Danchenko St., Novosibirsk 630087



References

1. Shnayder N.A. Cognitive dysfunction in young patients after operation under general anesthesia (prevalence, diagnostics, therapy and prevention). Sibirskoe meditsinskoe obozrenie = Siberian Medical Review 2006;(4):107-8. (In Russ.).

2. Suzuki J. Moyamoya disease. Sendai: Springer-Verlag Berlin Heidelberg, 1986. P. 189.

3. Yonekawa Y. Outer diameter measured by 3D CISS MRI and quasi-Moyamoya disease. Acta Neurochir (Wien) 2012;154(12):2159-61. DOI: 10.1007/s00701-012-1495-x.

4. Baba T., Houkin K., Kuroda S. Novel epidemiological features of moyamoya disease. J Neural Neurosurg Psychiatry 2008;79(8):900-4. DOI: 10.1136/jnnp.2007.130666.

5. Smith E.R., Scott R.M. Spontaneous occlusion of the circle of Willis in children: pediatric moyamoya summary with proposed evidence-based practice guidelines. A review. J Neurosurg Pediatr 2012;9(4):353-60. DOI: 10.3171/2011.12.PEDS1172.

6. Maximova M.Y., Zagrebina I.A., Krotenkova M.V., Davidenko I.S. Moyamoya disease. Atmosfera. Nervnye bolezni = Atmosphere. Nervous Disease 2010;(1):21-4. (In Russ.).

7. Wakai K., Tamakoshi A., Ikezaki K. Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey. Clin Neurol Neurosurg 1997;99 Suppl 2:S1-5. DOI: 10.1016/s0303-8467(97)00031-0.

8. Surgery of cerebral aneurysms. Ed. by V.V. Krylov. Moscow, 2011. Vol. 2. Pp. 492-493. (In Russ.).

9. Scott M.R., Smith E.R. Moyamoya disease and moyamoya syndrome. N Engl J Med 2009;360(12):1226-37. DOI: 10.1056/NEJMra0804622.

10. Houkin K., Kamiyama H., Takahashi A. et al. Combined revascularization surgery for childhood moyamoya disease: STA-MCA and encephalo-duro-arterio-myo-synangiosis. Childs Nerv Syst 1997;13(1):24-9. DOI: 10.1007/s003810050034.

11. Wang L., Qian C., Yu X. et al. Indirect bypass surgery may be more beneficial for symptomatic patients with moyamoya disease at early Suzuki stage. World Neurosurg 2016;95:304-8. DOI: 10.1016/j.wneu.2016.07.087.

12. Arias E.J., Derdeyn C.P., Dacey RG. Jr, Zipfel G.J. Advances and surgical considerations in the treatment of moyamoya disease. Neurosurgery 2014;74 Suppl 1:S116-25. DOI: 10.1227/NEU.0000000000000229.

13. Suzuki J., Takaku A. Cerebrovascular “moyamoya” disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol 1969;20(3):288-99.

14. Panuncev V.S., Hristoforova M.I. Features of clinic, diagnostics and treatment of patients with Moya-Moya disease and syndrome. Neyrokhirurgiya = Russian Journal of Neurosurgery 2001;(3):12-9. (In Russ.). DOI: 10.1227/NEU.0000000000000229.

15. Khachatryan W.A., Litvinenko P.V. Indirect revascularization surgery in children with symptomatic epilepsy. Neiyrokhirurgiya i nevrologiya detskogo vozrasta = Pediatric Neurosurgery and Neurology 2016;(4):47-58. (In Russ.).

16. Choi J.I., Ha S.K., Lim D.J., Kim S.D. Differential clinical outcomes following encephaloduroarteriosynangiosis in pediatric moyamoya disease presenting with epilepsy or ischemia. Childs Nerv Syst 2015;31(5):713-20. DOI: 10.1007/s00381-015-2666-x.

17. Takeuchi S., Takasato Y. Ischemic stroke following intracranial hemorrhage from moyamoya disease. Acta Neurochir (Wien) 2011;153(6):1271. DOI: 10.1007/s00701-011-0984-7.

18. Mikami T., Ochi S., Houkin K. et al. Predictive factors for epilepsy in moyamoya disease. J Stroke Cerebrovasc Dis 2015;24(1):17-23. DOI: 10.1016/j.jstrokecerebrovasdis.2014.07.050.

19. Houkin K., Mikami T. Moyamoya disease and moyamoya syndrome. In: Moyamoya disease: diagnosis and treatment. Ed. by J.E. Wanebo, N. Khan, J.M. Zabramski, R.F. Spetzler. New York, Stuttgart: Thieme, 2014. Pp. 3-9.

20. Chiu D., Shedden P., Bratina P., Grotta J.C. Clinical features of moyamoya disease in the United States. Stroke 1998;29(7):1347-51. DOI: 10.1161/01.STR.29.7.1347.

21. Shirane R., Yoshida Y., Takahashi T., Yoshimoto T. Assessment of encephalo-galeo-myo-synangiosis with dural pedicle insertion in childhood moyamoya disease: characteristics of cerebral blood flow and oxygen metabolism. Clin Neurol Neurosurg 1997;99 Suppl 2:S79-85. DOI: 10.1016/s0303-8467(97)00062-0.

22. Lee S., Rivkin M.J., Kirton A. et al. Moyamoya disease in children: results from the International Pediatric Stroke Study. J Child Neurol 2017;32(11):924-9. DOI: 10.1177/0883073817718730.

23. Matsushima Y., Aoyagi M., Masaoka H. et al. Mental outcome following encephaloduroarteriosynangiosis in children with moyamoya disease with the onset earlier than 5 years of age. Childs Nerv Syst 1990;6(8):440-3. DOI: 10.1007/BF00302089.

24. Tanabe N., Yamamoto S., Kashiwazaki D. et al. Indocyanine green visualization of middle meningeal artery before craniotomy during surgical revascularization for moyamoya disease. Acta Neurochir (Wien) 2017;159(3):567-75. DOI: 10.1007/s00701-016-3060-5.

25. Xu B. Surgical techniques individualized extracranial-intracranial revascularization in the treatment of late-stage Moyamoya disease. In: Surgical techniques in moyamoya vasculopathy: tricks of the trade. Ed. by P. Vajkoczy. Stuttgart, New York, Delhi, Rio de Janeiro: Thieme, 2020. Pp. 136-149.

26. Matsushima T., Fukui M., Kitamura K. et al. Encephalo-duro-arterio-synangiosis in children with moyamoya disease. Acta Neurochir (Wien) 1990;104(3-4):96-102. DOI: 10.1007/BF01842826.

27. Bot G.M., Burkhardt J., Gupta N., Lawton M.T. Superficial temporal artery-to-middle cerebral artery bypass in combination with indirect revascularization in moyamoya patients <3 years of age. J Neurosurg Pediatr 2019;23(2):198-203. DOI: 10.3171/2018.9.peds18224.

28. Czabanka M., Pena-Tapia P., Schubert G.A. et al. Characterization of cortical microvascularization in adult moyamoya disease. Stroke 2008;39(6): 1703-9. DOI: 10.1161/STROKEAHA.107.501759.

29. Veeravagu A., Guzman R., Patil C.G. et al. Moyamoya disease in pediatric patients: outcomes of neurosurgical interventions. Neurosurg Focus 2008;24(2):E16. DOI: 10.3171/FOC/2008/24/2/E16.

30. Gadgil N., Lam S., Pyarali M. et al. Indirect revascularization with the dural inversion technique for pediatric moyamoya disease: 20-year experience. J Neurosurg Pediatr 2018;22:541-9. DOI: 10.3171/2018.5.PEDS18163.

31. Smith E. Encephalo-duro-arterio-synangiosis: Pediatric. In: Surgical techniques in moyamoya vasculopathy: tricks of the trade. Ed. by P. Vajkoczy. Stuttgart, New York, Delhi, Rio de Janeiro: Thieme, 2020. Pp. 32-39.

32. Hecht N., Vajkoczy P. Encephalo-myo-synangiosis. In: Surgical techniques in moyamoya vasculopathy: tricks of the trade. Ed. by P. Vajkoczy. Stuttgart, New York, Delhi, Rio de Janeiro: Thieme, 2020. Pp. 25-31.

33. Imai H., Miyawaki S., Ono H. et al. The importance of encephalo-myo-synangiosis in surgical revascularization strategies for moyamoya disease in children and adults. World Neurosurg 2015;83(5):691-9. DOI: 10.1016/j.wneu.2015.01.016.

34. Zhao Y., Lu J., Yu S. et al. Comparison of long-term effect between direct and indirect bypass for pediatric ischemic-type moyamoya disease: a propensity score-matched study. Front Neurol 2019;10:795. DOI: 10.3389/fneur.2019.00795.

35. Kazumata K., Ito M., Tokairin K., Ito Y. et al. The frequency of postoperative stroke in moyamoya disease following combined revascularization: a singleuniversity series and systematic review. J Neurosurg 2014;121(2):432-40.

36. Kuroda S., Houkin K., Ishikawa T. et al. Novel bypass surgery for moyamoya disease using pericranial flap: its impacts on cerebral hemodynamics and long-term outcome. Neurosurgery 2010;66(6):1093-101. DOI: 10.1227/01.NEU.0000369606.00861.91.

37. Czabanka M., Vajkoczy P. Combined STA-MCA bypass and encephalo-myo-synangiosis. In: Surgical techniques in moyamoya vasculopathy: tricks of the trade. Ed. by P. Vajkoczy. Stuttgart, New York, Delhi, Rio de Janeiro: Thieme, 2020. Pp. 94-99.

38. Uchino H., Kim J., Fujima N. et al. Synergistic interactions between direct and indirect bypasses in combined procedures: the significance of indirect bypasses in moyamoya disease. Neurosurgery 2017;80(2):201-9. DOI: 10.1227/NEU.0000000000001201.

39. Amin-Hanjani S., Singh A., Rifai H. et al. Combined direct and indirect bypass for moyamoya: quantitative assessment of direct bypass flow over time. Neurosurgery 2013;73(6):962-7. DOI: 10.1227/NEU.0000000000000139.

40. Kuroda S. STA-MCA anastomosis and EDMAPS. In: Surgical techniques in moyamoya vasculopathy: tricks of the trade. Ed. by P. Vajkoczy. Stuttgart, New York, Delhi, Rio de Janeiro: Thieme, 2020. Pp. 116-125.

41. Shevchenko E.V., Usachev D.Yu., Belousova O.B. et al. Pediatric stroke. Revascularization and reconstructive operations in children with cerebrovascular pathology. Moscow: Izdatelskie resheniya, 2018. 141 p.

42. Amin-Hanjani S. STA-MCA bypass and encephalo-duro-arterio-synangiosis. In: Surgical techniques in moyamoya vasculopathy: tricks of the trade. Ed. by P. Vajkoczy. Stuttgart, New York, Delhi, Rio de Janeiro: Thieme, 2020. Pp. 126-135.

43. Yu L., He H., Zhao J. et al. More precise imaging analysis and diagnosis of moyamoya disease and moyamoya syndrome using high-resolution magnetic resonance imaging. World Neurosurg 2016;96:252-260. DOI: 10.1016/j.wneu.2016.08.083.

44. Tolani A.T., Yeom K.W., Elbers J. et al. Focal cerebral arteriopathy: the face with many names. Pediatr Neurol 2015;53(3):247-52. DOI: 10.1016/j.pediatrneurol.2015.05.008.


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For citations:


Ovsiannikov K.S., Dubovoy A.V., Rzaev D.A. Differentiated method in surgical revascularization of the brain for the treatment of pediatric patients with moyamoya angiopathy. Russian journal of neurosurgery. 2020;22(4):28-42. (In Russ.) https://doi.org/10.17650/1683-3295-2020-22-4-28-42

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ISSN 1683-3295 (Print)
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