Results 41 to 50 of about 294,742 (337)

Surgical lobectomy of pulmonary arteriovenous malformations in a patient with presentations regarded as sequela of tuberculosis: a case report

Journal of Cardiothoracic Surgery, 2020
Background Pulmonary arteriovenous malformations are uncommon conditions of abnormal communications between pulmonary arteries and veins, which are most commonly congenital in nature.
Peng Teng, Weidong Li, Yiming Ni
doaj   +1 more source

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

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia [PDF]

, 2001
BACKGROUND: Most patients with familial primary pulmonary hypertension have defects in the gene for bone morphogenetic protein receptor II (BMPR2), a member of the transforming growth factor beta (TGF-beta) superfamily of receptors. Because patients with
Alessandra Manes, Carl Atkinson, Cool CD, Cottingham RW, D'Alonzo GE, Gerald Simonneau, Ingrid Winship, James E. Loyd, Jennifer R. Thomson, Jonathan Berg, Julie McGaughran, Lisa Wheeler, Loyd JE, Makowski GS, Marc Humbert, Michael Pauciulo, Morse JH, Nazzareno Galie, Neil V. Morgan, Nicholas W. Morrell, Pietra GG, Rajiv D. Machado, Rich S, Richard C. Trembath, Whyte MK, William C. Nichols   +25 more
core   +1 more source

Malformações arteriovenosas do lobo parietal: revisão clínico-cirúrgica de 17 casos

Arquivos de Neuro-Psiquiatria, 1968
The incidence, clinical occurences, diagnosis and surgical procedures registered in 17 cases of arteriovenous malformations of the parietal lobe are reported. The authors conclude: The arteriovenous anomalies located in the parietal lobe were mostly (65%)
Nelson Pires Ferreira, Sérgio Raupp, João A. M. Dahne   +2 more
doaj   +1 more source

Intracranial dural arteriovenous fistula successfully treated by combined open-endovascular procedure [PDF]

, 2010
Intracranial dural arteriovenous fistulas constitute a rare though potentially devastating disease. Because the arterial (high-pressure) blood flow drains directly into the low-pressure venous system, there is a high risk of bleeding and associated ...
DE KEUKELEIRE, KATRIEN, Defreyne, Luc, Hallaert, Giorgio, Van Roost, Dirk, Vanhauwaert, Dimitri J   +4 more
core   +2 more sources

A nationwide cohort study on incidence and mortality associated with extracranial vascular malformations

Scientific Reports, 2023
Extracranial vascular malformations are abnormal formations of blood vessels located outside the brain (extracranial) that develop during fetal development.
Jeong Yeop Ryu, Yong June Chang, Joon Seok Lee, Kang Young Choi, Jung Dug Yang, Seok-Jong Lee, Jongmin Lee, Seung Huh, Ji Yoon Kim, Ho Yun Chung   +9 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

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

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

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