Results 71 to 80 of about 1,555,246 (206)

Cystic Medial Degeneration Leading to Popliteal Artery Aneurysm With Distal Embolization

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Cystic medial degeneration is a rare process that can cause aneurysmal degeneration of arteries including the aorta, iliac arteries, femoral arteries, and popliteal arteries. In this report we discuss a case of a popliteal artery aneurysm caused by cystic medial necrosis that led to distal embolization.
Victor Cabrera‐Bou, Tuleagh Innes‐Gawn, Adam Levitt, Julio Calderin   +3 more
wiley   +1 more source

Successful coil embolization for rupture of the subclavian artery associated with Ehlers-Danlos syndrome type IV [PDF]

, 2009
Ehlers-Danlos syndrome is a rare inherited disease of connective tissue. Patients with type IV Ehlers-Danlos syndrome are likely to present with arterial disorders such as aneurysm or dissection.
Obitsu, Yukio, Shigematsu, Hiroshi, Komai, Hiroyoshi, Iida, Yasunori   +3 more
core   +1 more source

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   +1 more source

A 27-Year-Old Woman With Postpartum Papillary Muscle Rupture

JACC: Case Reports, 2020
Postpartum papillary muscle rupture (PMR) is extremely uncommon and tolerated poorly with limited management options other than emergency surgical intervention.
Erika Hutt, MD, Celeste Santos-Martins, MD, Jose Aguilera, MD, Per Wierup, MD, PhD, Vidyasagar Kalahasti, MD, Carmela Tan, MD   +5 more
doaj   +1 more source

Prenatally diagnosed cleft lip and palate: Prenatal findings, clinical outcomes, genetic results, and sequencing yield in isolated versus non‐isolated cases

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract Introduction Cleft lip and palate (CLP) are common congenital disruptions of the orofacial cleft and are associated with numerous genetic conditions. This study examines prenatal findings, clinical outcomes, and genetic findings among prenatally diagnosed CLP, with a focus on the yield of next‐generation sequencing (NGS).
Thomas P. Kishkovich, Gabriela F. Tessler, Meghan Angley, Yijia Zhang, Thomas A. Imahiyerobo, Sherelle L. Laifer‐Narin, Hong Ma, Lynn Simpson, Caitlin D. Baptiste, Jessica L. Giordano, Russell S. Miller, Ronald J. Wapner   +11 more
wiley   +1 more source

Subclavian artery pseudoaneurysm in type IV Ehlers-Danlos Syndrome [PDF]

, 1998
We report case of a subclavian artery pseudoaneurysm in a patient with type IV Ehlers-Danlos Syndrome. A 16-year-old boy underwent successful repair of a subclavian artery pseudoaneurysm that occurred after a cervical hyperextension injury.
Rossi, Peter I., Friedman, Steven G., Scher, Larry A., Boxer, Robert A., Bialer, Martin G., Hall, Michae H.   +5 more
core   +1 more source

Bilateral carotid artery dissection due to Eagle syndrome in a patient with vascular Ehlers-Danlos syndrome: a case report

BMC Neurology, 2020
Background Patients with vascular Ehlers-Danlos syndrome (EDS) occasionally suffer from arterial dissection. Eagle syndrome, which is caused by an elongated styloid process and also causes arterial dissection, is difficult to diagnose and could sometimes
Hajime Ikenouchi, Masahito Takagi, Ayako Nishimura, Eriko Yamaguchi, Junpei Koge, Kozue Saito, Kazunori Toyoda, Masatoshi Koga   +7 more
doaj   +1 more source

A novel mutation in COL3A1 associates to vascular Ehlers–Danlos syndrome with predominant musculoskeletal involvement

Molecular Genetics & Genomic Medicine, 2021
Background Vascular Ehlers–Danlos syndrome (vEDS) is a heritable connective tissue disorder caused by defects in the type III collagen protein. It is generally considered the most severe form of Ehlers–Danlos syndrome (EDS) due to an increased risk of ...
Federica Ruscitti, Lucia Trevisan, Giulia Rosti, Fabio Gotta, Annalia Cianflone, Alessandro Geroldi, Paola Origone, Anna Pichiecchio, Simona Viglio, Maria Iascone, Paola Mandich   +10 more
doaj   +1 more source

The vascular aneurysms of Ehlers-Danlos syndrome type IV [PDF]

European Heart Journal, 2011
A 32-year-old woman presented with severe left flank pain. On physical examination, the skin was so thin and pale that subcutaneous blood vessels were visible. An abdominal computed tomographic (CT) scan showed multiple renal infarctions in the left kidney and dissection with thrombus in aneurysmal dilated renal artery (diameter 8.1 mm) ( Panel A ...
Jae-Youn, Moon, Soo-Jin, Lee, Tae Soo, Kang   +2 more
openaire   +2 more sources

Multiple External Invasive Root Resorption and Calcification in Systemic Sclerosis—Case Report

International Endodontic Journal, Volume 59, Issue 9, Page 1963-1978, September 2026.
ABSTRACT Aim There are few reports in the literature of multiple external invasive root resorption (EIRR) lesions in patients with systemic sclerosis (SSc), and an association between root resorption and SSc is not well established. We report the only case that comprehensively illustrates—with the combination of histopathology, cone beam computed ...
Jee‐Yun Leung, Geoffrey Heithersay, Richard Logan, Sharon Liberali   +3 more
wiley   +1 more source