prikaz prve stranice dokumenta Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association
  Download
PDF 126.63 KB
Scientific paper - Original scientific paper
Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association
Collegium Antropologicum, 35 (2011), S. 1; 333-338. urn:nbn:hr:105:894773
Šarac, Helena; Telarović, Srđana; Markeljević, Jasenka; Perić, Berislav; Pavliša, Goran; Radoš, Marko

Institutional repository: Dr Med - University of Zagreb School of Medicine Digital Repository

Cite this document

Šarac, H., Telarović, S., Markeljević, J., Perić, B., Pavliša, G. & Radoš, M. (2011). Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association . Collegium Antropologicum, 35. (S. 1), 333-338. Retrieved from https://urn.nsk.hr/urn:nbn:hr:105:894773

Šarac, Helena, et al. "Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ." Collegium Antropologicum, vol. 35, no. S. 1, 2011, pp. 333-338. https://urn.nsk.hr/urn:nbn:hr:105:894773

Šarac, Helena, Srđana Telarović, Jasenka Markeljević, Berislav Perić, Goran Pavliša and Marko Radoš. "Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ." Collegium Antropologicum 35, no. S. 1 (2011): 333-338. https://urn.nsk.hr/urn:nbn:hr:105:894773

Šarac, H., et al. (2011) 'Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ', Collegium Antropologicum, 35(S. 1), pp. 333-338. Available at: https://urn.nsk.hr/urn:nbn:hr:105:894773 (Accessed 29 November 2024)

Šarac H, Telarović S, Markeljević J, Perić B, Pavliša G, Radoš M. Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association . Collegium Antropologicum [Internet]. 2011 January [cited 2024 November 29];35(S. 1):333-338. Available at: https://urn.nsk.hr/urn:nbn:hr:105:894773

H. Šarac, S. Telarović, J. Markeljević, B. Perić, G. Pavliša and M. Radoš, "Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ", Collegium Antropologicum, vol. 35, no. S. 1, pp. 333-338, January 2011. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:105:894773. [Accessed: 29 November 2024]

Metadata
Title (english)Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association
Title (croatian)Simptomatska kapilarna teleangiektazija ponsa i intracerebralna razvojna venska anomalija: prikaz slučaja
AuthorHelena Šarac
AuthorSrđana Telarović
AuthorJasenka Markeljević
AuthorBerislav Perić
AuthorGoran Pavliša
AuthorMarko Radoš
Author's institutionUniversity of Zagreb
School of Medicine
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Abstract (english)
Various combinations of vascular malformations of the brain in one lesion have been reported, while others seem to be very rare. In this report, the authors discuss the case of a coexistence of an capillary telangiectasia of the pons and intracerebral venous anomaly. To our knowledge, this is the first report of coexistence of a capillary telangiectasia of the pons and intracerebral venous anomaly apparted from each other. These discrete vascular malformations of the brain raise attention on possible interrelations in the pathogenesis of these entities. We report a case of pontine capillary telangiectasia and intracerebral venous anomaly in a 42-year-old woman with a right side facial palsy. Hight field magnetic resonance imaging suggested presence of a capillary telangiectasia of the pons. Another lesion in the left frontal gyrus was attributable to the venous anomaly. Along with neuroradiological findings, results of the somatosensor evoked potentials, brain stem auditory potentials, laboratory analysis including blood, cerebrospinal fluid and urine investigation are demonstrated. Awareness of the magnetic resonance imaging finding of the capillary telangiectasias and of the venous anomalies may help in defining clinical correlates of this vascular malformations, while the follow up of these malformations might help to asses risk of vascular rupture. We and others previously selects capillary telangiectasia and venous anomaly in two discrete entities. Coexistence of these malformations in the brain apparted from each other appear to be very rare and raise attention on possible interactions in their natural history and pathogenesis.
Abstract (croatian)
Do sada su opisivane različite kombinacije krvožilnih malformacija mozga unutar jedne lezije, dok su ostale kombinacije vjerojatno vrlo rijetke. U ovom članku, autori raspravljaju primjer koegzistencije kapilarne telangiektazije u ponsu i intracerebralne venske anomalije. Prema našim spoznajama, ovo je prvi slučaj u kojem se opisuje istovremena prisutnost kapilarne telangiektazije i razvojne venske anomalije mozga udaljene jedna od druge. Ove diskretne vaskularne malformacije mozga pobuđuju na razmišljanje o mogućoj povezanosti patogeneza ovih dvaju entiteta. Opisujemo slučaj kapilarne telangiektazije u ponsu i intracerebralne venske anomalije u 42-godišnje bolesnice s paralizom desne polovice lica. Magnetska rezonancija pokazala je kapilarnu telangiektaziju u ponsu, dok druga lezija u lijevom čeonom girusu odgovara razvojnoj venskoj anomaliji. Uz neuroradiološke nalaze, prezentirani su i rezultati somatosenzornih evociranih potencijala (SSEP), auditornih potencijala moždanog debla (BAEP), laboratorijske nalaze krvi, urina i cerebrospinalnog likvora. Prepoznavanje nalaza kapilarne telangiektazije i venske anomalije na magnetskoj rezonanciji može pomoći u definiranju kliničkih poveznica obiju vaskularnih malformacija, dok praćenje ovih malformacija može pomoći u procjeni rizika od vaskularne rupture. Mi i drugi prije nas, izdvajamo kapilarne telangiektazije i razvojne venske anomalije u dva diskretna entiteta. Koegzistencija ovih malformacija u mozgu odvojeno jedna od druge, pobuđuje zanimanje o mogućim interakcijama u njihovom nastanku, patogenezi i terapijskim mogućnostima.
Keywords (english)
Languageenglish
Publication typeScientific paper - Original scientific paper
Publication statusPublished
Peer reviewPeer review
Publication versionPublished version
Journal titleCollegium Antropologicum
Numberingvol. 35, no. S. 1, pp. 333-338
p-ISSN0350-6134
URN:NBNurn:nbn:hr:105:894773
Publication2011-01
Document URLhttps://hrcak.srce.hr/64108
Type of resourceText
Access conditionsOpen access
Terms of useLicence In copyright icon
Created on2024-03-28 12:04:45