Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report

Nephrotic syndrome (NS) is a hypercoagulable state in which children are at risk of venous thromboembolism. A higher risk has been reported in children with steroid-resistant NS than in those with steroid-sensitive NS. The mortality rate of cerebral venous sinus thrombosis (CVST) is approximately 10...

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Main Authors: Se Jin Park, Haing-Woon Baik, Myung Hyun Cho, Ju Hyung Kang
Format: Article
Language:English
Published: Korean Society of Pediatric Nephrology 2022-12-01
Series:Childhood Kidney Diseases
Subjects:
Online Access:http://chikd.org/upload/pdf/ckd-22-041.pdf
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author Se Jin Park
Haing-Woon Baik
Myung Hyun Cho
Ju Hyung Kang
author_facet Se Jin Park
Haing-Woon Baik
Myung Hyun Cho
Ju Hyung Kang
author_sort Se Jin Park
collection DOAJ
description Nephrotic syndrome (NS) is a hypercoagulable state in which children are at risk of venous thromboembolism. A higher risk has been reported in children with steroid-resistant NS than in those with steroid-sensitive NS. The mortality rate of cerebral venous sinus thrombosis (CVST) is approximately 10% and generally results from cerebral herniation in the acute phase and an underlying disorder in the chronic phase. Our patient initially manifested as a child with massive proteinuria and generalized edema. He was treated with albumin replacement and diuretics, angiotensin-converting enzyme inhibitor, and deflazacort. Non-contrast computed tomography showed areas of hyperattenuation in the superior sagittal sinus when he complained of severe headache and vomiting. Subsequent magnetic resonance imaging revealed empty delta signs in the superior sagittal, lateral transverse, and sigmoid sinuses, suggesting acute CVST. Immediate anticoagulation therapy was started with unfractionated heparin, antithrombin III replacement, and continuous antiproteinuric treatment. The current report describes a life-threatening CVST in a child with steroid-dependent NS, initially diagnosed by contrast non-enhanced computed tomography and subsequently confirmed by contrast-enhanced magnetic resonance imaging, followed by magnetic resonance venography for recanalization, addressing successful treatment.
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spelling doaj.art-0b6f6faffe7e43528374487dfed504d62023-03-02T06:33:50ZengKorean Society of Pediatric NephrologyChildhood Kidney Diseases2384-02422384-02502022-12-0126210110610.3339/ckd.22.041777Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case reportSe Jin Park0Haing-Woon Baik1Myung Hyun Cho2Ju Hyung Kang3 Department of Pediatrics, Daejeon Eulji Medical Center, Eulji University School of Medicine, Daejeon, Republic of Korea Department of Biochemistry, Eulji University School of Medicine, Daejeon, Republic of Korea Department of Pediatrics, Hallym University Sacred Heart Hospital, Anyang, Republic of Korea Department of Pediatrics, Daejeon Eulji Medical Center, Eulji University School of Medicine, Daejeon, Republic of KoreaNephrotic syndrome (NS) is a hypercoagulable state in which children are at risk of venous thromboembolism. A higher risk has been reported in children with steroid-resistant NS than in those with steroid-sensitive NS. The mortality rate of cerebral venous sinus thrombosis (CVST) is approximately 10% and generally results from cerebral herniation in the acute phase and an underlying disorder in the chronic phase. Our patient initially manifested as a child with massive proteinuria and generalized edema. He was treated with albumin replacement and diuretics, angiotensin-converting enzyme inhibitor, and deflazacort. Non-contrast computed tomography showed areas of hyperattenuation in the superior sagittal sinus when he complained of severe headache and vomiting. Subsequent magnetic resonance imaging revealed empty delta signs in the superior sagittal, lateral transverse, and sigmoid sinuses, suggesting acute CVST. Immediate anticoagulation therapy was started with unfractionated heparin, antithrombin III replacement, and continuous antiproteinuric treatment. The current report describes a life-threatening CVST in a child with steroid-dependent NS, initially diagnosed by contrast non-enhanced computed tomography and subsequently confirmed by contrast-enhanced magnetic resonance imaging, followed by magnetic resonance venography for recanalization, addressing successful treatment.http://chikd.org/upload/pdf/ckd-22-041.pdfanticoagulantscase reportsmagnetic resonance angiographynephrotic syndromethrombosis
spellingShingle Se Jin Park
Haing-Woon Baik
Myung Hyun Cho
Ju Hyung Kang
Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
Childhood Kidney Diseases
anticoagulants
case reports
magnetic resonance angiography
nephrotic syndrome
thrombosis
title Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
title_full Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
title_fullStr Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
title_full_unstemmed Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
title_short Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
title_sort acute dural venous sinus thrombosis in a child with idiopathic steroid dependent nephrotic syndrome a case report
topic anticoagulants
case reports
magnetic resonance angiography
nephrotic syndrome
thrombosis
url http://chikd.org/upload/pdf/ckd-22-041.pdf
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