2020
DOI: 10.1080/14767058.2020.1731466
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Prenatal diagnosis and treatment of intrahepatic arteriovenous fistulas: case reports and the literature review

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Cited by 9 publications
(12 citation statements)
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“…HAVMs are rare congenital lesions consisting of hepatic artery-portal vein fistula and hepatic artery-hepatic venous malformation. There have been only 8 reports of HAVMs in fetuses with typical imaging in ultrasonography in the previous literature, [ 3 , 4 ] but no MRI imaging data were provided. HAVMs are reported to be associated with HHT, which is inherited as an autosomal dominant disease caused by mutations in ENG, ACVRL1, or SMAD-4 genes.…”
Section: Discussionmentioning
confidence: 99%
“…HAVMs are rare congenital lesions consisting of hepatic artery-portal vein fistula and hepatic artery-hepatic venous malformation. There have been only 8 reports of HAVMs in fetuses with typical imaging in ultrasonography in the previous literature, [ 3 , 4 ] but no MRI imaging data were provided. HAVMs are reported to be associated with HHT, which is inherited as an autosomal dominant disease caused by mutations in ENG, ACVRL1, or SMAD-4 genes.…”
Section: Discussionmentioning
confidence: 99%
“…Prenatal treatment including propranolol or corticosteroids may be helpful, as described in one case report. 24 Follow-up examinations should be carried out depending on size of the vascular malformation, extent of the perfusion, and signs of high cardiac output failure (severe cardiomegaly, AV valve insufficiency, and hydrops fetalis, respectively) in order to identify progression and to time delivery and therapeutic intervention. Acute prenatal deterioration from time of diagnosis is not generally expected and should be considered when initiating corticosteroid prophylaxis or timing delivery, as these lesions are non-proliferating vascular anomalies that grow proportionally to fetal weight.…”
Section: Discussionmentioning
confidence: 99%
“…Early prenatal diagnosis of intrahepatic AVM is important as it might change management and outcome of affected fetuses. Prenatal treatment including propranolol or corticosteroids may be helpful, as described in one case report 24 . Follow‐up examinations should be carried out depending on size of the vascular malformation, extent of the perfusion, and signs of high cardiac output failure (severe cardiomegaly, AV valve insufficiency, and hydrops fetalis, respectively) in order to identify progression and to time delivery and therapeutic intervention.…”
Section: Discussionmentioning
confidence: 99%
“…Although the radio-cephalic AVF is the recommended initial access for hemodialysis, the radial artery at the volar wrist and the brachial artery at the antecubital fossa and medial upper arm are usual anatomical locations for stula development (4). In some of the cases, lower extremity AVF is approached secondary to upper extremity AVF failure.…”
Section: Introductionmentioning
confidence: 99%
“…The ideal venous access would provide enough blood for the dialysis, be more durable, and have a low rate of complications (7). Complications such as stenosis, aneurysm, infection, and bleeding prevent AVF patency and lead to AVF de ciency (4,5). The incidence of AVF de ciency is increasing accordingly like cardiovascular disorder (7).…”
Section: Introductionmentioning
confidence: 99%