• Tidak ada hasil yang ditemukan

Other Extracranial Artery Involvement in Moyamoya Disease

Dalam dokumen Moyamoya Disease Update (Halaman 138-141)

In addition to the renal artery, the coronary [10, 23] , pulmonary [5, 7, 8, 11] , superior mesenteric [8, 21, 29] , pancreatic [7] , iliac [29] , and peripheral [6, 9] arteries have also been reported to be involved in moyamoya disease. However, there have been no reports of the prevalence of the involvement of major abdominal vessels except for the renal artery, and involvement of abdominal vessels other than the renal artery are considered less common.

References

1. Suzuki J, Takaku A (1969) Cerebrovascular “moyamoya” disease: disease showing abnormal net-like vessels in base of brain. Arch Neurol 20:288–299

2. Suzuki J, Kodama N (1983) Moyamoya disease: a review. Stroke 14:104–109

3. Nishimoto A, Takeuchi S (1968) Abnormal cerebrovascular network related to the internal carotid arteries. J Neurosurg 29:255–260

4. Scott RM, Smith ER (2009) Moyamoya disease and moyamoya syndrome. N Engl J Med 360:

1226–1237

5. Kapusta L, Daniëls O, Renier WO (1990) Moyamoya syndrome and primary pulmonary hypertension in childhood. Neuropediatrics 21:162–163

6. Goldenberg HJ (1974) “Moyamoya” associated with peripheral vascular occlusive disease. Arch Dis Child 49:964–966

7. Ikeda E (1991) Systemic vascular changes in spontaneous occlusion of the circle of Willis. Stroke 22:1358–1362

8. De Vries RR, Nikkels PG, van der Laag J et al (2003) Moyamoya and extracranial vascular involvement:

fibromuscular dysplasia? A report of two children. Neuropediatrics 34:318–321

9. Weber C, Tatò F, Brandl T et al (2001) Adult moyamoya disease with peripheral artery involvement.

J Vasc Surg 34:943–946

10. Komiyama M, Nishikawa M, Yasui T et al (2001) Moyamoya disease and coronary artery disease – case report. Neurol Med Chir (Tokyo) 41:37–41

11. Ou P, Dupont P, Bonnet D (2006) Fibromuscular dysplasia as the substrate for systemic and pulmonary hypertension in the setting of Moya-Moya disease. Cardiol Young 16:495–497

12. Godin M, Helias A, Tadie M et al (1978) Moyamoya syndrome and renal artery stenosis. Kidney Int 15:450

13. Ellison PH, Largent JA, Popp AJ (1981) Moya-moya disease associated with renal artery stenosis.

Arch Neurol 38:467

14. Terasawa K, Yamaguchi Y, Ishihara O et al (1983) Moya-moya disease associated with fibromuscular dysplasia of renal artery. No To Hattatsu 15:350–355

15. Yamashita M, Tanaka K, Kishikawa T et al (1984) Moyamoya disease associated with renovascular hypertension. Hum Pathol 15:191–193

16. Halley SE, White WB, Ramsby GR et al (1988) Renovascular hypertension in moyamoya syndrome.

Therapeutic response to percutaneous transluminal angioplasty. Am J Hypertens 1:348–352 17. Jansen JN, Donker AJ, Luth WJ et al (1990) Moyamoya disease associated with renovascular

hypertension. Neuropediatrics 21:44–47

18. Rupprecht T, Wenzel D, Schmitzer E et al (1992) Diagnosis of moyamoya disease with additional renal artery stenosis by colour coded Doppler sonography. Pediatr Radiol 22:527–528

19. Nakano T, Azuma E, Ido M et al (1993) Moyamoya disease associated with bilateral renal artery stenosis. Acta Paediatr Jpn 35:354–357

131 Systemic Arterial Involvement in Moyamoya Disease

20. Van der Vliet JA, Zeilstra DJ, Van Roye SF et al (1994) Renal artery stenosis in moyamoya syndrome.

J Cardiovasc Surg (Torino) 35:441–443

21. Shoskes DA, Novick AC (1995) Surgical treatment of renovascular hypertension in moyamoya disease: case report and review of the literature. J Urol 153:450–452

22. Takagi Y, Hashimoto N, Goto Y (1997) Haemodynamic ischaemia in paediatric moyamoya disease associated with renovascular hypertension. Acta Neurochir (Wien) 139:257–258

23. Akasaki T, Kagiyama S, Omae T et al (1998) Asymptomatic moyamoya disease associated with coronary and renal artery stenosis – a case report. Jpn Circ J 62:136–138

24. Kuwayama F, Hamasaki Y, Shinagawa T et al (2001) Moyamoya disease complicated with renal artery stenosis and nephrotic syndrome: reversal of nephrotic syndrome after nephrectomy. J Pediatr 138:418–420

25. Caldarelli M, Di Rocco C, Gaglini P (2001) Surgical treatment of moyamoya disease in pediatric age. J Neurosurg Sci 45:83–91

26. Hoshino Y, Nakano A, Oguri M et al (2001) Intravascular ultrasound detects coarctation of the renal artery in a patient with Moyamoya disease. Hypertens Res 24:283–287

27. Fuchs FD, Francesconi CR, Caramori PR et al (2001) Moyamoya disease associated with renovascular disease in a young African-Brazilian patient. J Hum Hypertens 15:499–501

28. Kaczorowska M, Jóźwiak S, Litwin M et al (2005) Moyamoya disease associated with stenosis of extracranial arteries: a case report and review of the literature. Neurol Neurochir Pol 39:242–246 29. Choi Y, Kang BC, Kim KJ et al (1997) Renovascular hypertension in children with moyamoya disease.

J Pediatr 131:258–263

30. Yamada I, Himeno Y, Matsushima Y et al (2000) Renal artery lesions in patients with moyamoya disease. Angiographic findings. Stroke 31:733–737

31. Togao O, Mihara F, Yoshiura T et al (2004) Prevalence of stenoocclusive lesions in the renal and abdominal arteries in moyamoya disease. Am J Radiol 183:119–122

32. Safian RD, Textor SC (2001) Renal artery stenosis. N Engl J Med 344:431–442

33. Castellote E, Romero R, Bonet J et al (1995) Takayasu’s arteritis as a cause of renovascular hypertension in a non-Asian population. J Hum Hypertens 9:841–845

34. Hosoda Y (1984) Pathology of so-called “spontaneous occlusion of the circle of Willis.” Pathol Annu 2:221–244

35. Deal JE, Snell MF, Barratt TM et al (1992) Renovascular disease in childhood. J Pediatr 121:378–384 36. Ellis D, Shapiro R, Scantleburg VP et al (1995) Evaluation and management of bilateral renal artery

stenosis in children: a case series and review. Pediatr Nephrol 9:259–267

132

Introduction

Moyamoya disease is a chronic, occlusive cerebrovascular disease with unknown etiology, characterized by bilateral steno-occlusive changes at the terminal portion of the internal carotid artery and an abnormal vascular network at the base of the brain [1] . The association of moyamoya disease with further neurosurgical diseases, such as cerebral aneurysms [2– 5] , brain tumors, cervical carotid artery stenosis, and cerebrovascular malformations, has been described previously [6– 11] . It is well known that moyamoya disease is frequently associated with intracranial aneurysms located within the abnormal basal network or the circle of Willis, which are explained by the intrinsic pathology of moyamoya disease, such as hemodynamic stress and fragile structure of the collateral vessels [2– 5] . On the other hand, the association with atherosclerotic cervical carotid artery stenosis or with brain tumors leads to the diagnosis of akin moyamoya disease (quasi-moyamoya disease) according to the diagnostic criteria of the Research Committee on Spontaneous Occlusion of the Circle of Willis, of the Ministry of Health, Labor, and Welfare, Tokyo, Japan. The coincidence of moyamoya disease with cere- bral vascular malformations including arteriovenous malformation [6, 7] , cerebral cavernous malformation [8– 10] , and venous malformation [10] has been reported in the literature. A rare association of with dural arteriovenous fistula is also demonstrated [11] . In this chapter, we especially focus on the association of moyamoya disease with further cerebrovascular disease based on our experience.

M. Fujimura (!)

Department of Neurosurgery , Kohnan Hospital , 4-20-1 Nagamachi-minami, Taihaku-ku , Sendai , 982-8523 , Japan

e-mail: [email protected] T. Tominaga

Department of Neurosurgery , Tohoku University Graduate School of Medicine , Sendai , Japan

Associated Neurosurgical Diseases

Miki Fujimura and Teiji Tominaga

B.-K. Cho and T. Tominaga (eds.), Moyamoya Disease Update, DOI 10.1007/978-4-431-99703-0_21, © Springer 2010

133 Associated Neurosurgical Diseases

Dalam dokumen Moyamoya Disease Update (Halaman 138-141)