Results 41 to 50 of about 88,843 (236)

Pulmonary arteriovenous malformation [PDF]

open access: yesPostgraduate Medical Journal, 2002
Abstract Pulmonary arteriovenous malformations (PAVM) are rare pulmonary vascular anomalies. Although most patients are asymptomatic, PAVMs can cause dyspnoea from right-to-left shunt. Because of paradoxical emboli, various central nervous system complications have been described including stroke and brain abscess.
I, Khurshid, G H, Downie
openaire   +2 more sources

Transvenous arteriovenous malformation embolization

open access: yes, 2020
Transvenous embolization of arteriovenous malformations has emerged as a safe and effective intervention. In carefully selected patients the transvenous approach has shown efficacy similar to that of conventional transarterial routes. The optimal lesions
Brahimaj, Bledi C   +2 more
core   +1 more source

Spontaneous Hemothorax by Pulmonary Arteriovenous Malformation during Pregnancy

open access: yesThe Thoracic & Cardiovascular Surgeon Reports, 2023
Background: Pulmonary arteriovenous malformation (PAVM) is a rare vascular malformation that may cause hemothorax, especially during pregnancy.
Chuxiao Duan, Yunfei Mu, Yi Yang
doaj   +1 more source

Acquired Chiari malformation type I associated with a supratentorial fistulous arteriovenous malformation: a case report

open access: yes, 2017
A case of acquired Chiari malformation type I with frontal fistulous arteriovenous malformation (AVM) is presented, and the pathophysiology is discussed. The tonsillar herniation and hydrocephalus both resolved after AVM was excised.
杜永光;郭夢菲;李崇維   +1 more
core   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston   +6 more
wiley   +1 more source

Uterine Arteriovenous Malformation As A Rare Cause Of Menorrhagia [PDF]

open access: yes, 2008
Uterine arterio venous malformation is uncommon cause of menorrhagia.
Sudipta Chakraborty   +7 more
core  

Hemiretinal vein occlusion secondary to arteriovenous malformation

open access: yesThe Pan-American Journal of Ophthalmology, 2017
Purpose: To describe an hemiretinal vein obstruction secondary to a congenital arteriovenous malformation. Methods: Case report of a young patient with retinal arteriovenous malformation and hemiretinal vein obstruction.
Badr O AlAhmadi, J Fernando Arévalo
doaj   +3 more sources

Ruptured arteriovenous malformation secondary to placental site trophoblastic tumor: A diagnostic dilemma and its successful management

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2018
Placental site trophoblastic tumor is a very rare neoplasm and is a subtype of gestational trophoblastic neoplasm. Owing to its rarity and varied clinical manifestations, it can lead to a diagnostic dilemma.
Avantika Gupta   +2 more
doaj   +1 more source

Arteriovenous malformation with pseudoaneurysm on the left upper limb

open access: yesClinical Case Reports, 2022
A 61‐year‐old woman developed a pulsatile mass on the left upper limb and was diagnosed with arteriovenous malformation with pseudoaneurysm. A two‐stage operation including ligation and resection of the aberrant branches and subsequent resection of the ...
Akihisa Furuta   +4 more
doaj   +1 more source

High Diagnosis Rate for Nonimmune Hydrops Fetalis With Prenatal Clinical Genome: Expanded Results From the Hydrops‐Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nonimmune hydrops fetalis (NIHF) is characterized by abnormal fluid accumulation in ≥ 2 fetal compartments and may be genetic. The incremental diagnostic yield of prenatal exome sequencing (ES) for NIHF following a negative standard workup was previously explored on 22 cases.
Stephanie M. Rice   +10 more
wiley   +1 more source

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