Literature DB >> 33973836

Hereditary Hemorrhagic Telangiectasia: The Convergence of Genotype, Phenotype, and Imaging in Modern Diagnosis and Management of a Multisystem Disease.

Steven W Hetts1, Joseph T Shieh1, Michael A Ohliger1, Miles B Conrad1.   

Abstract

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease that manifests as vascular malformations in the brain, lung, liver, gastrointestinal tract, nasal mucosa, and skin. Diagnosis and management of HHT is guided in large part by imaging studies, making it a condition with which the radiology community needs familiarity. Proper screening and care lead to improved morbidity and mortality in patients with HHT. International guidelines were recently updated and form the basis for a detailed discussion of the role of imaging and image-guided therapy in HHT. © RSNA, 2021 Online supplemental material is available for this article.

Entities:  

Year:  2021        PMID: 33973836     DOI: 10.1148/radiol.2021203487

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  5 in total

Review 1.  Imaging to intervention: a review of what the Interventionalist needs to Know about Hereditary Hemorrhagic Telangiectasia.

Authors:  Stephanie Sobrepera; Eric Monroe; Joseph J Gemmete; Danial Hallam; Jason W Pinchot; Claire Kaufman
Journal:  CVIR Endovasc       Date:  2021-12-09

2.  Rendú Osler Weber Syndrome; case report.

Authors:  Oscar Manuel García Córdova; Tania Cristina Pérez Morales; Verónica Andrea Del Pilar Barón Hernández; José Sebastián Sotelo Cuéllar
Journal:  Radiol Case Rep       Date:  2022-06-19

3.  Liver involvement in a hereditary hemorrhagic telangiectasia patient with Gd-EOB-DTPA enhanced MRI: a case description.

Authors:  Jiahui Jiang; Xiaoming Wang; Dawei Yang; Zhenghan Yang
Journal:  Quant Imaging Med Surg       Date:  2022-09

4.  Case Report: Clinical characteristics and genetic analysis of two patients with hereditary hemorrhagic telangiectasia.

Authors:  Qiu-Ying Wang; Yu-Xuan Feng; Ying-Wei Zhu; Yu-Xia Sun; Jing-Duan Xu; Hui-Min Shi; Yi-Min Mao; Hong-Wei Jiang
Journal:  Front Genet       Date:  2022-08-25       Impact factor: 4.772

5.  Case report: Diagnosis of hereditary hemorrhagic telangiectasia (Osler Weber Rendu Syndrome) in a 23-year-old male presented with anemia and thrombocytopenia and its response to bevacizumab.

Authors:  Hamza Yunus; Said Amin; Furqan Ul Haq; Waqar Ali; Tanveer Hamid; Wajid Ali; Basharat Ullah; Payal Bai
Journal:  Front Med (Lausanne)       Date:  2022-10-03
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.