Results 51 to 60 of about 303,472 (356)

Twenty-seven years follow-up of a patient with congenital retinocephalofacial vascular malformation syndrome and additional congenital malformations (Bonnet-dechaume-blanc syndrome or wyburn-mason syndrome)

European Journal of Medical Research, 2010
Purpose Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. Methods MRI and cerebral angiography.
Schmidt D, Agostini H, Schumacher M
doaj   +1 more source

Pulmonary arteriovenous malformations: endovascular therapy.

Cardiovascular Diagnosis and Therapy, 2018
Pulmonary arteriovenous malformations (PAVM) are abnormal direct communications between the branches of pulmonary arteries and veins, and are often seen in patients with hereditary hemorrhagic telangiectasia (HHT).
M. Chamarthy, Harold S Park, P. Sutphin, G. Kumar, D. Lamus, S. Saboo, Matthew E. Anderson, S. Kalva   +7 more
semanticscholar   +1 more source

Pulmonary Arteriovenous Malformations [PDF]

American Journal of Respiratory and Critical Care Medicine, 2014
Within the past decade, pulmonary arteriovenous malformations (PAVMs) have evolved from rare curiosities to not uncommon clinical states, with the latest estimates suggesting a prevalence of ~1 in 2,600. PAVMs provide anatomic right-to-left shunts, allowing systemic venous blood to bypass gas exchange and pulmonary capillary bed processing.
openaire   +4 more sources

Diagnostic Pitfalls: Soft Tissue Lymphoma: Superficial Soft Tissue Lymphoma Mimicking a Venous Malformation

Journal of Vascular Anomalies
In this case report, 3 patients addressed to our vascular anomalies reference center to manage a slow-flow vascular anomaly were reported. Our objective is to highlight that a discrepancy between clinical and radiological data should suggest a ...
Victoire Roblot, Valérie Bousson, Annouk Bisdorff   +2 more
doaj   +1 more source

Complex Cerebrovascular Presentation in Central Nepal with Therapeutic Challenge

Nepal Journal of Neuroscience, 2016
Effective management of complex vascular malformation remains one of the more challenging problems faced in most of the developing countries where modern therapeutic resources are deficient.
Karuna T Karki , Pramod K Chaudhary , Binod Bhattarai , Sunil Munakomi   +3 more
doaj   +1 more source

Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia [PDF]

, 2015
Hereditary hemorrhagic telangiectasia (HHT) is mechanistically and therapeutically challenging, not only because of the molecular and cellular perturbations that generate vascular abnormalities, but also the modifications to circulatory physiology that ...
Shovlin, CL
core   +2 more sources

Engineered Microfluidic Organoid Systems: New Paradigms for Menopause Mechanism Research and Personalized Medicine

Advanced Materials Technologies, EarlyView.
This review explores the integration of microfluidic technology with organoid systems as an innovative platform for studying menopausea complex multi‐organ condition. By enabling precise simulation of inter‐organ communication and hormone responses, microfluidic organoids offer a physiologically relevant model for investigating menopausal syndrome and ...
Qianyi Zhang, He Huang, Hongliang Dong, Qiang Ma, Hongyan Jin   +4 more
wiley   +1 more source

Liver transplantation in a patient with hereditary haemorrhagic telangiectasia and pulmonary hypertension

Pulmonary Circulation, 2019
Hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber syndrome is a systemic vascular disease with autosomal dominant inheritance, mucocutaneous telangiectasia, and repeated nasal bleeding due to vascular abnormalities.
Kentaro Ejiri, Satoshi Akagi, Kazufumi Nakamura, Naofumi Amioka, Keishi Ichikawa, Takahito Yagi, Hiroshi Ito   +6 more
doaj   +1 more source

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

Journal of Pediatric Surgery Case Reports, 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.
Naruhiko Murase, Hiroo Uchida, Akihide Tanano, Chiyoe Shirota, Akinari Hinoki, Takahisa Tainaka, Kazuki Yokota, Kazuo Oshima, Ryo Shirotsuki   +8 more
doaj   +1 more source

Angiographic analysis on posterior fossa hemorrhages and vascular malformations beyond aneurysms by CT angiography and digital subtraction angiography

Egyptian Journal of Neurosurgery, 2022
Background Posterior fossa malformations are less common than supratentorial malformations, but hemorrhages in posterior fossa are more serious due to presence of vital structures within this region.
S. Vignesh, Surya Nandan Prasad, Vivek Singh, Zafar Neyaz, R. V. Phadke, Anant Mehrotra, Prabhakar Mishra   +6 more
doaj   +1 more source