prikaz prve stranice dokumenta Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases
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Scientific paper - Case study
Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases
Collegium Antropologicum, 35 (2011), S. 1; 319-325. urn:nbn:hr:105:896796
Telarović, Srđana; Šarac, Helena; Žagar, Marija; Markeljević, Jasenka; Vranješ, Davorka; Radoš, Marko

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Telarović, S., Šarac, H., Žagar, M., Markeljević, J., Vranješ, D. & Radoš, M. (2011). Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases . Collegium Antropologicum, 35. (S. 1), 319-325. Retrieved from https://urn.nsk.hr/urn:nbn:hr:105:896796

Telarović, Srđana, et al. "Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases ." Collegium Antropologicum, vol. 35, no. S. 1, 2011, pp. 319-325. https://urn.nsk.hr/urn:nbn:hr:105:896796

Telarović, Srđana, Helena Šarac, Marija Žagar, Jasenka Markeljević, Davorka Vranješ and Marko Radoš. "Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases ." Collegium Antropologicum 35, no. S. 1 (2011): 319-325. https://urn.nsk.hr/urn:nbn:hr:105:896796

Telarović, S., et al. (2011) 'Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases ', Collegium Antropologicum, 35(S. 1), pp. 319-325. Available at: https://urn.nsk.hr/urn:nbn:hr:105:896796 (Accessed 05 November 2024)

Telarović S, Šarac H, Žagar M, Markeljević J, Vranješ D, Radoš M. Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases . Collegium Antropologicum [Internet]. 2011 January [cited 2024 November 05];35(S. 1):319-325. Available at: https://urn.nsk.hr/urn:nbn:hr:105:896796

S. Telarović, H. Šarac, M. Žagar, J. Markeljević, D. Vranješ and M. Radoš, "Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases ", Collegium Antropologicum, vol. 35, no. S. 1, pp. 319-325, January 2011. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:105:896796. [Accessed: 05 November 2024]

Metadata
Title (english)Coexistence of intradural spinal arteriovenous malformation and associated developmental anomalies – report of two cases
Title (croatian)Intraduralna spinalna atriovenska maformacija udružena s razvojnim anomalijama: prikaz dva slučaja
AuthorSrđana Telarović
AuthorHelena Šarac
AuthorMarija Žagar
AuthorJasenka Markeljević
AuthorDavorka Vranješ
AuthorMarko Radoš
Author's institutionUniversity of Zagreb
School of Medicine
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Abstract (english)
Spinal arteriovenous malformations (AVM) have been devided into dural (Type I), intramedullary glomus (Type II), juvenile (Type III), and perimedullary direct arteriovenous fistulae (Type IV). AVMs are usually associated with subacute myelopathy in what has been known as Foix-Alajouanine syndrome.We presented two patients with two intradural spinal arteriovenous malformations associated in what we call Foix-Alajouanine syndrome. The both patient developed acute back pain and paresthesias, followed by paraplegia and incontinence. The clinical status of one patient has been improved after particle embolization for a 17 years when he deteriorated up to paraplegia after spinal angiography for follow up. Clinical status in another patient deteriorated, because particle emoblisation cannot be performed due to very descrete presentation of the feeding artery. Extensive neuroradiological examination in both patients revealed coexistence of numerous associated developmental anomalies in both patients.We conclude that arteriovenous malformations occasionally are associated with other vascular and nonvascular developmental anomalies elsewhere in the body. These findings rise attention about keep in mind the suspicion of mutual etiopathogenesis and congenital origin of these anomalies. Early timing of the diagnostic and therapeutic interventiosn are stressed to prevent or delay irreversible ishaemic myellopathy or haemorrhage. For the definitive diagnosis of spinal arteriovenous malformations and evaluation of its occlusion grade after the therapy spinal angiography is needed.
Abstract (croatian)
Spinalne arteriovenske malformacije su klasificirane u intraduralne (Tip I), intramedularni glomus (Tip II), juvenilne (Tip III) i perimedularne direktne arteriovenske fistule (Tip IV). Arteriovenske malformacije su obično udružene sa subakutnom mijelopatijom u sindromu Foix-Alajouanine. U ovoj studiji, opisuju se dijagnostičke i terapijske procedure u dva bolesnika sa spinalnom arteriovenskom malformacijom i Foix-Alajouanin sindromom. Oba bolesnika u početku su imali simptome akutne boli u leđima i parestezije, a potom se stanje klinički pogoršalo do potpune paraplegije i inkontinencije. Jedan bolesnik bio je klinički stabilan 17 godina nakon višekratnih postupaka endovaskularne embolizacije, ali je nakon zadnjeg rutinskog postupka kontrolne spinalne angiografije doživio kliničko pogoršanje do potpune paraplegije, vjerojatno uslijed vazospazma. Kod drugog bolesnika klinički status se progresivno pogoršavao do parapareze budući da se terapijska endovaskularna embolizacija nije mogla provesti zbog izrazito diskretne prezentacija »hranidbenih« arterija. Opsežna radiološka obrada u oba bolesnika otkrila je niz konkomitantnih razvojnih anomalija. Iz ovih podataka možemo zaključiti da spinalne arteriovenske malformacije mogu ponekad biti udružene s drugim krvožilnim i drugim razvojnim malformacijama, ne samo u centralnom živčanom sustavu nego u bilo kojem dijelu tijela. Iz toga slijedi da kod bolesnika kod kojih se objektivizira spinalna arteriovenska malformacija, treba biti učinjena šira dijagnostička obrada. Iz ovoga se također može pretpostaviti da bi ove anomalije mogle imati zajedničku etiopatogenezu koja sugerira kongenitalno porijeklo i uzroke ovih razvojnih anomalija. Rana dijagnostika i terapijski postupci mogu spriječiti ili odgoditi ireverzibilnu ishemijsku mijelopatiju ili hemoragiju. Za konačnu dijagnozu spinalnih arteriovenskih malformacija i evaluaciju okluzija nakon terapijskog postupka neophodna je spinalna angiografija.
Keywords (english)
Languageenglish
Publication typeScientific paper - Case study
Publication statusPublished
Peer reviewPeer review
Publication versionPublished version
Journal titleCollegium Antropologicum
Numberingvol. 35, no. S. 1, pp. 319-325
p-ISSN0350-6134
URN:NBNurn:nbn:hr:105:896796
Publication2011-01
Document URLhttps://hrcak.srce.hr/64100
Type of resourceText
Access conditionsOpen access
Terms of useLicence In copyright icon
Created on2024-03-28 12:04:35