Výsledky vyhledávání - "Hepatic arteriovenous malformation"

Akademický článek

Thick tiny hearts and tangled vessels: Navigating the complexity of a neonate with hepatic arteriovenous malformation, hypertrophic cardiomyopathy, and persistent pulmonary hypertension

Autor: Shaifalika Thakur, Sunil Kishore, Rizwan Ahmar, Rakesh Kumar

Publikováno v: Heart India, Vol 12, Iss 1, Pp 52-54 (2024)

Congenital hepatic arteriovenous malformation (HAVM) is an uncommonly encountered condition in clinical practice. This condition often presents as isolated hepatomegaly, congestive cardiac failure or anemia. Here, we discuss a case of a full-term neo

Externí odkaz: https://doaj.org/article/735c8d929612477a9b31e15468a2ffbe

Zobrazit plný text záznamu

Akademický článek

Prenatal diagnosis and management of a giant intrahepatic arteriovenous malformation—Sonographic findings, clinical implications, and treatment

Autor: Adeline Walter, Elina Calite, Andreas Müller, Jörg C. Kalff, Carsten Meyer, Annegret Geipel, Ulrich Gembruch, Christine Schreiner

Publikováno v: Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)

Abstract Prenatal detection of complex giant hepatic arteriovenous malformation requires an examination of the affected fetal hemodynamic situation with emphasis on the affected arterial supply pattern. Early pediatric surgeon presentation is needed,

Externí odkaz: https://doaj.org/article/89505c0617ce457f8697b70198614dca

Zobrazit plný text záznamu

Akademický článek

Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia

Autor: Sophie Giraud, Claire Bardel, Sophie Dupuis-Girod, Marie-France Carette, Brigitte Gilbert-Dussardier, Sophie Riviere, Jean-Christophe Saurin, Mélanie Eyries, Sylvie Patri, Evelyne Decullier, Alain Calender, Gaëtan Lesca

Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)

Abstract Background Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by multiple telangiectases and caused by germline disease-causing variants in the ENG (HHT1), ACVRL1 (HHT2) and, to a lesser extent MADH4

Externí odkaz: https://doaj.org/article/6cb683a8210448e4a726913c553472f1

Zobrazit plný text záznamu

Plný text ve formátu HTML

Akademický článek

Endovascular embolization of canine hepatic arteriovenous malformations using precipitating hydrophobic injectable liquid (PHIL) liquid embolic agent: a proof of concept study

Autor: Stewart D. Ryan, Anjali Nambiar, Julian Maingard, Hong Kuan Kok, Robert B. S. Turner, Duncan Mark Brooks, Hamed Asadi

Publikováno v: CVIR Endovascular, Vol 2, Iss 1, Pp 1-8 (2019)

Abstract Background Hepatic arteriovenous malformations (HAVMs) are rare congenital lesions consisting of multiple high-pressure arteries feeding into low-pressure veins via a central nidus. Massive haemorrhage, portal hypertension and hepatic insuff

Externí odkaz: https://doaj.org/article/6adf599fd91142ba8e008199a1ea1c0a

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Severe Hypoxemia Caused by High-Output Heart Failure and Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia

Autor: Tomomi Yamaguchi, Hiroaki Yamamoto, Chieko Itamoto, Tomoki Koshyo

Publikováno v: JACC Case Reports

A man affected by hereditary hemorrhagic telangiectasia who had chronic severe hypoxemia is presented. This hypoxemia was synergistically caused by high-output heart failure due to severe hepatic shunts and multiple pulmonary arteriovenous shunts. Th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c48d37a98a9dc714528db8a461d1793
http://europepmc.org/articles/PMC8642735

Zobrazit plný text záznamu

Akademický článek

Emergency hepatectomy for hepatic arteriovenous malformation combined with pulmonary hypertension in an infant

Autor: Naruhiko Murase, Hiroo Uchida, Akihide Tanano, Chiyoe Shirota, Akinari Hinoki, Takahisa Tainaka, Kazuki Yokota, Kazuo Oshima, Ryo Shirotsuki

Publikováno v: Journal of Pediatric Surgery Case Reports, Vol 3, Iss 12, Pp 534-536 (2015)

Patients with hepatic arteriovenous malformations rarely present with pulmonary hypertension. We report the case of a 3-month-old boy who developed severe pulmonary hypertension due to a hepatic arteriovenous malformation. The use of pulmonary vasodi

Externí odkaz: https://doaj.org/article/19d22f7633f34bf8bfbf48cbb4ef9663

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia

Autor: Giraud, Sophie, Bardel, Claire, Dupuis-Girod, Sophie, Carette, Marie-France, Gilbert-Dussardier, Brigitte, Riviere, Sophie, Saurin, Jean-Christophe, Eyries, Mélanie, Patri, Sylvie, Decullier, Evelyne, Calender, Alain, Lesca, Gaëtan

Publikováno v: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2020, 15 (1), pp.254. ⟨10.1186/s13023-020-01533-2⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), pp.254. ⟨10.1186/s13023-020-01533-2⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)

International audience; Abstract Background Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by multiple telangiectases and caused by germline disease-causing variants in the ENG (HHT1) , ACVRL1 (HHT2) and,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fc799354cc227e21015658741974d236
https://hal.science/hal-04074937

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání