Results 11 to 20 of about 1,915,528 (208)

Iatrogenic distal aortic rupture in a patient with vascular Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2023
Vascular Ehlers-Danlos syndrome is a rare inherited connective tissue disorder that can result in significant morbidity and mortality. This report details an iatrogenic aortic rupture during an endovascular approach in the management of critical limb ...
Mohammad M. Zagzoog, MD, Sean A. Crawford, MD, Thomas Le Houérou, MD, Antoine Gaudin, MD, Stéphan Haulon, MD, PhD, Dominique Fabre, MD, PhD   +5 more
doaj   +2 more sources

Vascular Ehlers-Danlos syndrome with distinct histopathologic features [PDF]

Journal of Pathology and Translational Medicine, 2022
Ehlers-Danlos syndrome is a connective tissue disorders that presents with heterogeneous manifestations depending on the involved genes. Vascular Ehlers-Danlos syndrome (vEDS), also known as Ehlers-Danlos syndrome type IV, is caused by a heterozygous ...
Hee Sang Hwang, Jin Woo Song, Se Jin Jang   +2 more
openaire   +4 more sources

Late conversion after endovascular abdominal aortic aneurysm repair in a patient with Ehlers-Danlos syndrome

Journal of Vascular Surgery Cases and Innovative Techniques, 2019
Vascular Ehlers-Danlos syndrome is associated with life-threatening events. The management of the disease is challenging because of the emergency presentation of symptoms and the tissue friability of the aorta.
Georgios Karaolanis, MD, MSc, PhD, Özgun Sensebat, MD, Giovanni Torsello, MD, Theodosios Bisdas, MD, Konstantinos P. Donas, MD   +4 more
doaj   +2 more sources

Rupture of a Median Sacral Artery Aneurysm in a Patient with Vascular Ehlers Danlos Syndrome [PDF]

EJVES Vascular Forum, 2020
Introduction: Vascular Ehlers Danlos syndrome is a rare connective tissue disease that is associated with various arterial complications. Report: A 25 year old man with vascular Ehlers Danlos syndrome presented with acute lower back pain as a result of a
Merel J. Verhagen, Rutger W. van der Meer, Carla S.P. van Rijswijk, Jan van Schaik   +3 more
doaj   +2 more sources

Vascular type Ehlers‐Danlos syndrome with intra‐abdominal hemorrhage due to ruptured hepatic aneurysm: A case report

Acute Medicine & Surgery
Background Vascular Ehlers‐Danlos syndrome has a high mortality rate due to hemorrhagic complications. Case Presentation We report a case of vascular‐type Ehlers‐Danlos syndrome diagnosed due to rupture of multiple celiac aneurysms.
Masaou Tanaka, Kentaro Ueda, Takafumi Yonemitsu, Shinobu Tamura, Akira Ikoma, Tetsuo Sonomura, Shigeaki Inoue   +6 more
doaj   +2 more sources

A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report

Clinical Case Reports, 2023
Kyphoscoliotic Ehlers–Danlos syndrome (kEDS) is a rare genetic disorder combining congenital hypotonia, congenital/early onset and progressive kyphoscoliosis, and generalized joint hypermobility.
Malika Foy, Corinne Métay, Michael Frank, Nicolas Denarié, Salma Adham, Clarisse Billon, Anne Legrand, Xavier Jeunemaitre, Fabrice Gillas, Karen Gaudon, Philippe De Mazancourt, Ahmed Mekki, Robert Carlier, Karelle Benistan   +13 more
doaj   +2 more sources

Vascular Ehlers-Danlos syndrome

Revista Portuguesa de Cardiologia, 2022
Marta Marques
doaj   +3 more sources

Ehlers–Danlos Syndrome: Not Just Joint Hypermobility

Case Reports in Medicine, 2018
Ehlers–Danlos syndrome is an umbrella term for a group of heritable soft connective tissue disorders which is characterized by joint hypermobility, skin texture and elasticity abnormalities, and visceral and vascular fragility or dysfunctions.
Tina Bregant, Milica Klopcic Spevak
doaj   +2 more sources

Iliac artery dissection and rupture in a patient with classic Ehlers-Danlos syndrome due to COL5A1 null variant

Journal of Vascular Surgery Cases and Innovative Techniques
This is a case of a 46-year-old woman who presented with right common iliac artery dissection preceded by a left common iliac artery dissection and rupture 6 years earlier. Both iliac arteries required repair.
Amit Pujari, MD, Sherene Shalhub, MD, MPH, FACS, DFSVS   +1 more
doaj   +2 more sources

Concurrent Splenic Peliosis and Vascular Ehlers-Danlos Syndrome

Annals of Vascular Surgery, 2009
This case report describes concurrent splenic peliosis and vascular Ehlers-Danlos syndrome (EDS) in a 59-year-old male patient. After splenic rupture due to peliosis, the complicated postoperative period hinted at the possibility of vascular EDS. This diagnosis was confirmed by genetic testing, which revealed a novel point mutation in the COL3A1 gene ...
Bon, A.C. van, Kristinsson, J.O., Krieken, J.H.J.M. van, Wanten, G.J.A.   +3 more
openaire   +4 more sources