A rare pediatric case of portal vein aneurysm thrombosis

Portal vein aneurysm (PVA) is rarely encountered, and published papers describing this etiology in adults and children typically include only case reports or small case series. We present a clinical case of PVA in a child associated with severe complications, including diffuse thrombosis of the port...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Tran Thanh Tri, MD, PhD, Ho Phi Duy, MD, Bui Hai Trung, MD, Luu-Nguyen An Thuan, MD, Pham Ngoc Thach, MD, PhD, Nguyen Xuan Hien, MD, PhD, Nguyen Minh Duc, MD, MSc
Formato: article
Lenguaje:EN
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://doaj.org/article/8e89bc36804b45e9b414bac224a50114
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8e89bc36804b45e9b414bac224a50114
record_format dspace
spelling oai:doaj.org-article:8e89bc36804b45e9b414bac224a501142021-11-26T04:26:33ZA rare pediatric case of portal vein aneurysm thrombosis1930-043310.1016/j.radcr.2021.10.065https://doaj.org/article/8e89bc36804b45e9b414bac224a501142022-02-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S1930043321007846https://doaj.org/toc/1930-0433Portal vein aneurysm (PVA) is rarely encountered, and published papers describing this etiology in adults and children typically include only case reports or small case series. We present a clinical case of PVA in a child associated with severe complications, including diffuse thrombosis of the portal venous system. A 10-year-old boy presented with abdominal pain and vomiting, resulting in an initial diagnosis of pancreatic head tumor based on suspicious images on abdominal grayscale ultrasound. Contrast-enhanced computed tomography confirmed a diagnosis of occlusive PVA thrombosis (36 × 37 × 95 mm). Lacking drastic symptoms, the patient was treated with conservative anticoagulant therapy. On follow-up, the thrombosis appeared to shrink gradually and disappeared at 6 months based on Doppler ultrasound imaging. The PVA was reduced in size, and hepatopetal flow was restored. Surgeons and radiologists should be aware of this rare entity to ensure that a precise diagnosis can be established and to provide suitable treatment.Tran Thanh Tri, MD, PhDHo Phi Duy, MDBui Hai Trung, MDLuu-Nguyen An Thuan, MDPham Ngoc Thach, MD, PhDNguyen Xuan Hien, MD, PhDNguyen Minh Duc, MD, MScElsevierarticlePortal vein aneurysmThrombosisAnticoagulant therapyMedical physics. Medical radiology. Nuclear medicineR895-920ENRadiology Case Reports, Vol 17, Iss 2, Pp 286-289 (2022)
institution DOAJ
collection DOAJ
language EN
topic Portal vein aneurysm
Thrombosis
Anticoagulant therapy
Medical physics. Medical radiology. Nuclear medicine
R895-920
spellingShingle Portal vein aneurysm
Thrombosis
Anticoagulant therapy
Medical physics. Medical radiology. Nuclear medicine
R895-920
Tran Thanh Tri, MD, PhD
Ho Phi Duy, MD
Bui Hai Trung, MD
Luu-Nguyen An Thuan, MD
Pham Ngoc Thach, MD, PhD
Nguyen Xuan Hien, MD, PhD
Nguyen Minh Duc, MD, MSc
A rare pediatric case of portal vein aneurysm thrombosis
description Portal vein aneurysm (PVA) is rarely encountered, and published papers describing this etiology in adults and children typically include only case reports or small case series. We present a clinical case of PVA in a child associated with severe complications, including diffuse thrombosis of the portal venous system. A 10-year-old boy presented with abdominal pain and vomiting, resulting in an initial diagnosis of pancreatic head tumor based on suspicious images on abdominal grayscale ultrasound. Contrast-enhanced computed tomography confirmed a diagnosis of occlusive PVA thrombosis (36 × 37 × 95 mm). Lacking drastic symptoms, the patient was treated with conservative anticoagulant therapy. On follow-up, the thrombosis appeared to shrink gradually and disappeared at 6 months based on Doppler ultrasound imaging. The PVA was reduced in size, and hepatopetal flow was restored. Surgeons and radiologists should be aware of this rare entity to ensure that a precise diagnosis can be established and to provide suitable treatment.
format article
author Tran Thanh Tri, MD, PhD
Ho Phi Duy, MD
Bui Hai Trung, MD
Luu-Nguyen An Thuan, MD
Pham Ngoc Thach, MD, PhD
Nguyen Xuan Hien, MD, PhD
Nguyen Minh Duc, MD, MSc
author_facet Tran Thanh Tri, MD, PhD
Ho Phi Duy, MD
Bui Hai Trung, MD
Luu-Nguyen An Thuan, MD
Pham Ngoc Thach, MD, PhD
Nguyen Xuan Hien, MD, PhD
Nguyen Minh Duc, MD, MSc
author_sort Tran Thanh Tri, MD, PhD
title A rare pediatric case of portal vein aneurysm thrombosis
title_short A rare pediatric case of portal vein aneurysm thrombosis
title_full A rare pediatric case of portal vein aneurysm thrombosis
title_fullStr A rare pediatric case of portal vein aneurysm thrombosis
title_full_unstemmed A rare pediatric case of portal vein aneurysm thrombosis
title_sort rare pediatric case of portal vein aneurysm thrombosis
publisher Elsevier
publishDate 2022
url https://doaj.org/article/8e89bc36804b45e9b414bac224a50114
work_keys_str_mv AT tranthanhtrimdphd ararepediatriccaseofportalveinaneurysmthrombosis
AT hophiduymd ararepediatriccaseofportalveinaneurysmthrombosis
AT buihaitrungmd ararepediatriccaseofportalveinaneurysmthrombosis
AT luunguyenanthuanmd ararepediatriccaseofportalveinaneurysmthrombosis
AT phamngocthachmdphd ararepediatriccaseofportalveinaneurysmthrombosis
AT nguyenxuanhienmdphd ararepediatriccaseofportalveinaneurysmthrombosis
AT nguyenminhducmdmsc ararepediatriccaseofportalveinaneurysmthrombosis
AT tranthanhtrimdphd rarepediatriccaseofportalveinaneurysmthrombosis
AT hophiduymd rarepediatriccaseofportalveinaneurysmthrombosis
AT buihaitrungmd rarepediatriccaseofportalveinaneurysmthrombosis
AT luunguyenanthuanmd rarepediatriccaseofportalveinaneurysmthrombosis
AT phamngocthachmdphd rarepediatriccaseofportalveinaneurysmthrombosis
AT nguyenxuanhienmdphd rarepediatriccaseofportalveinaneurysmthrombosis
AT nguyenminhducmdmsc rarepediatriccaseofportalveinaneurysmthrombosis
_version_ 1718409914606419968