Literature DB >> 15368138

Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia -- results of extensive screening.

E Buscarini1, C Danesino, C Olivieri, G Lupinacci, F De Grazia, L Reduzzi, P Blotta, P Gazzaniga, F Pagella, M Grosso, G Pongiglione, L Buscarini, H Plauchu, A Zambelli.   

Abstract

AIMS: In previous studies, the prevalence of hepatic vascular malformations (VMs) in a large Italian family with hereditary hemorrhagic telangiectasia (HHT) was examined by Doppler ultrasonography (US) as screening technique, and the relevant Doppler US findings were described and classified. Thereafter, Doppler US has been routinely used to screen HHT families for liver involvement. Hepatic VMs were evaluated and classified on the basis of Doppler US findings.
METHODS: Three hundred and forty-six subjects belonging to 64 pedigrees were checked for the presence of signs of HHT. All of them underwent abdominal Doppler US screening for hepatic VMs. Vascular abnormalities were classified as minimal if the hepatic artery was dilated in extrahepatic tract only and measured > 6 mm; as moderate if the hepatic artery was dilated in both intra and extrahepatic tract; and as severe if complex changes of the arterial hepatic branches were associated with hepatic and/or portal vein dilatation. Furthermore, Doppler parameters, both qualitative (flow direction, turbulence) and quantitative (peak flow velocity and resistivity index in hepatic artery, mean velocity in portal vein, diastolic peak flow velocity in hepatic veins), were entered into our VM classification.
RESULTS: HHT was found in 222 subjects, with hepatic VMs detected by Doppler US in 92 (41.4 %) (24 males, 68 females, mean age 52.2). Hepatic VMs were minimal in 11 subjects, moderate in 70, and severe in 11.
CONCLUSIONS: On the basis of our proposed grading, hepatic VMs can be easily classified in subjects with HHT by Doppler US. Depending on the degree of hepatic vascular derangement, appropriate programs for follow up and/or therapy can be designed.

Entities:  

Mesh:

Year:  2004        PMID: 15368138     DOI: 10.1055/s-2004-813549

Source DB:  PubMed          Journal:  Ultraschall Med        ISSN: 0172-4614            Impact factor:   6.548


  17 in total

1.  [64-year old patient with tachycardia and signs of heart failure].

Authors:  M M Zaruba; T Waggershauser; S Weckbach; A Gerbes; O Mühling; S Kääb
Journal:  Internist (Berl)       Date:  2009-04       Impact factor: 0.743

Review 2.  Hereditary hemorrhagic telangiectasia of the liver complicated by ischemic bile duct necrosis and sepsis: case report and review of the literature.

Authors:  Anastasios Mavrakis; Anthony Demetris; Erin Rubin Ochoa; Mordechai Rabinovitz
Journal:  Dig Dis Sci       Date:  2009-09-16       Impact factor: 3.199

Review 3.  Signs and genetics of rare cancer syndromes with gastroenterological features.

Authors:  William Bruno; Giuseppe Fornarini; Paola Ghiorzo
Journal:  World J Gastroenterol       Date:  2015-08-14       Impact factor: 5.742

4.  Symptomatic liver involvement in neonatal hereditary hemorrhagic telangiectasia.

Authors:  Suhail Al-Saleh; Philip R John; Michelle Letarte; Marie E Faughnan; Jaques Belik; Felix Ratjen
Journal:  Pediatrics       Date:  2011-05-02       Impact factor: 7.124

5.  Liver involvement in hereditary hemorrhagic telangiectasia: can breath test unmask impaired hepatic first-pass effect?

Authors:  Marcello Candelli; Maurizio Pompili; Patrizia Suppressa; Gennaro M Lenato; Giulia Bosco; Gian Ludovico Rapaccini; Antonio Gasbarrini; Arnaldo Scardapane; Carlo Sabbà
Journal:  Intern Emerg Med       Date:  2011-02-09       Impact factor: 3.397

6.  Pulmonary hypertension in hereditary haemorrhagic telangiectasia.

Authors:  Veronique Mm Vorselaars; Sebastiaan Velthuis; Repke J Snijder; Jan Albert Vos; Johannes J Mager; Martijn C Post
Journal:  World J Cardiol       Date:  2015-05-26

Review 7.  Cardiac and Hemodynamic Manifestations of Hereditary Hemorrhagic Telangiectasia.

Authors:  Ahmed Farhan; Muhammad A Latif; Anum Minhas; Clifford R Weiss
Journal:  Int J Angiol       Date:  2022-07-09

Review 8.  Recognizing genetic disease: A key aspect of pediatric pulmonary care.

Authors:  Lael M Yonker; Megan H Hawley; Peter P Moschovis; Mengdi Lu; T Bernard Kinane
Journal:  Pediatr Pulmonol       Date:  2020-07

9.  Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia.

Authors:  Elisabetta Buscarini; Gioacchino Leandro; Dario Conte; Cesare Danesino; Erica Daina; Guido Manfredi; Guido Lupinacci; Gianfranco Brambilla; Fernanda Menozzi; Federico De Grazia; Pietro Gazzaniga; Giuseppe Inama; Roberto Bonardi; Pasquale Blotta; Pierangelo Forner; Carla Olivieri; Annalisa Perna; Maurizio Grosso; Giacomo Pongiglione; Edoardo Boccardi; Fabio Pagella; Giorgio Rossi; Alessandro Zambelli
Journal:  Dig Dis Sci       Date:  2011-02-03       Impact factor: 3.199

Review 10.  Optimal management of hereditary hemorrhagic telangiectasia.

Authors:  Neetika Garg; Monica Khunger; Arjun Gupta; Nilay Kumar
Journal:  J Blood Med       Date:  2014-10-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.