1,936
Views
2
CrossRef citations to date
0
Altmetric
Case Reports

Fatal spontaneous rupture of common iliac artery associated with fibromuscular dysplasia

, , , , , , , , & show all
Pages 358-363 | Received 15 Jul 2016, Accepted 15 Dec 2016, Published online: 31 Jan 2017

References

  • Dolak W, Maresch J, Kainberger F, et al. Fibromuscular dysplasia mimicking Crohn's disease over a period of 23 years. J Crohn's Colitis. 2012;6:354–357.
  • Lummus S, Breeze R, Lucia MS, et al. Histopathologic features of intracranial vascular involvement in fibromuscular Dysplasia, Ehlers-Danlos Type IV, and Neurofibromatosis I. J Neuropathol Exp Neurol. 2014;73:916–932.
  • Poloskey SL, Olin JW, Mace P, et al. Fibromuscular dysplasia. Circulation. 2012;125:e636–e639.
  • Perdu J, Boutouyrie P, Bourgain C, et al. Inheritance of arterial lesions in renal fibromuscular dysplasia. J Hum Hypertens. 2007;21:393–400.
  • Shivapour DM, Erwin P, Kim ESH. Epidemiology of fibromuscular dysplasia: a review of the literature. Vasc Med. 2016;21:376–381.
  • Grau R. Pseudovasculitis: mechanisms of vascular injury and clinical spectrum. Curr Rheumatol Rep. 2002;4:83–89.
  • Siegert CE, Macfarlane JD, Hollander AM, et al. Systemic fibromuscular dysplasia masquerading as polyarteritis nodosa. Nephrol Dial Transplant. 1996;11:1356–1358.
  • Pontes Tde C, Rufino GP, Gurgel MG, et al. Fibromuscular dysplasia: a differential diagnosis of vasculitis. Rev Bras Reumatol. 2012;52:70–74.
  • Yoshioka I, Arichi N, Tokugawa S, et al. Spontaneous rupture of common iliac artery associated with fibromuscular dysplasia presenting with colic pain suggestive of ureteral stone. Hinyokika Kiyo. 2007;53:721–724.
  • Slovut DP, Olin JW. Fibromuscular dysplasia. N Engl J. 2004;350:1862–1871.
  • Rastogi N, Kabutey NK, Kim D, et al. Symptomatic fibromuscular dysplasia of the external iliac artery. Ann Vasc Surg. 2012;26:574.e9–574.e13.
  • Bornak A, Milner R. Diagnosing and treating atypical arterial pathologies of aortic arch vessels: dissection and fibromuscular dysplasia. Semin Vasc Surg. 2011;24:36–43.
  • van de Nes JA, Bajanowski T, Trübner K. Fibromuscular dysplasia of the basilar artery: an unusual case with medico-legal implications. Forensic Sci Int. 2007;173:188–192.
  • Akashi H, Nata S, Kanaya K, et al. Spontaneous dissection of the iliac artery in a patient with fibromuscular dysplasia. Ann Vasc Surg. 2010;24:952.e13–952.e16.
  • Honjo O, Yamada Y, Kuroko Y, et al. Spontaneous dissection and rupture of common iliac artery in a patient with fibromuscular dysplasia: a case report and review of the literature on iliac artery dissections secondary to fibromuscular dysplasia. J Vasc Surg. 2004;40:1032–1036.
  • Teh LG, Sieunarine K, Van Schie G, et al. Spontaneous common iliac artery dissection after exercise. J Endovasc Ther. 2003;10:163–166.
  • Savolainen H, Heller G, Fleischmann A, et al. Spontaneous dissection of common iliac artery: a case report. Vasc Endovasc Surg. 2004;38:263–265.
  • Hey A, Röckelein G. Arterial fibromuscular dysplasia as an unexpected cause of death in adults. Dtsch Med Wochenschr. 1987;112:1819–1822.
  • Burri B, Fontolliet C, Ruegsegger CH, et al. External iliac artery dissection due to fibromuscular dysplasia. Vasa. 1983;12:76–78.
  • Sauer L, Reilly LM, Goldstone J, et al. Clinical spectrum of symptomatic external iliac fibromuscular dysplasia. J Vasc Surg. 1990;12:488–496.
  • Patel KS, Wolfe JH, Mathias C. Left external iliac artery dissection and bilateral renal artery aneurysms secondary to fibromuscular dysplasia: a case report. Neth J Surg. 1990;42:118–120.
  • Thevenet A, Latil JL, Albat B. Fibromuscular disease of the external iliac artery. Ann Vasc Surg. 1992;6:199–204.
  • Lück I, Hanschke D, Geissler C, et al. Spontaneous dissection of the external iliac artery due to fibromuscular dysplasia. Vasa. 2002;31:115–121.
  • Sugiura T, Imoto K, Uchida K, et al. Fibromuscular dysplasia associated with simultaneous spontaneous dissection of four peripheral arteries in a 30-year-old man. Ann Vasc Surg. 2011;25:838.e9–838.e11.
  • Ciura V, Bromley A, Wong J. A case of type A aortic dissection with underlying fibromuscular dysplasia. J Radiol Case Rep. 2011;5:22–28.
  • Radhi JM, McKay R, Tyrrell MJ. Fibromuscular dysplasia of the aorta presenting as multiple recurrent thoracic aneurysms. Int J Angiol. 1998;7:215–218.
  • Mukherjee D, Eagle KA. Aortic dissection – an update. Curr Probl Cardiol. 2005;30:287–325.
  • Criado FJ. Aortic dissection: a 250-year perspective. Tex Heart Inst J. 2011;38:694–700.
  • Lüscher TF, Keller HM, Imhof HG, et al. Fibromuscular hyperplasia: extension of the disease and therapeutic outcome results of the university hospital Zurich cooperative study on fibromuscular hyperplasia. Nephron. 1986;44(Suppl 1):109–114.
  • Prisant LM, Szerlip HM, Mulloy LL. Fibromuscular dysplasia: an uncommon cause of secondary hypertension. J Clin Hypertens (Greenwich). 2006;8:894–898.
  • Bolen MA, Brinza E, Renapurkar RD, et al. Screening CT angiography of the aorta, visceral branch vessels, and pelvic arteries in fibromuscular dysplasia. JACC Cardiovasc Imaging. 2016. Sep 16. pii: S1936-878X(16)30537-X. doi: 10.1016/j.jcmg.2016.04.010
  • Makino Y, Inokuchi G, Yokota H, et al. Sudden death due to coronary artery dissection associated with fibromuscular dysplasia revealed by postmortem selective computed tomography coronary angiography: a case report. Forensic Sci Int. 2015;253:e10–e15.
  • Vilariño Villaverde R, Bruguier C, et al. Tearing of the left iliac vessels in lumbar surgery revealed by multiphase post-mortem CT-angiography (MPMCTA). Leg Med (Tokyo). 2016;20:44–48.
  • Palmiere C, Binaghi S, Doenz F, et al. Detection of hemorrhage source: the diagnostic value of post-mortem CT-angiography. Forensic Sci Int. 2012;222:33–39.