1.Surgical Reconstruction of Traumatic Pseudoaneurysm of Palmar Arch Caused by Blunt Trauma
Nikolaos PAPATHEODOROU ; Konstantinos DIMITRIADIS ; Damianos DOUKAS ; Christos ARGYRIOU ; George S. GEORGIADIS
Vascular Specialist International 2022;38(4):30-
Although rare, pseudoaneurysms (PAs) of the palmar arch are mostly considered benign. However, they can cause severe complications if left untreated or misdiagnosed. There are a few data on traumatic PAs of the palmar arch, particularly those most commonly caused by penetrating hand injuries. However, PAs caused by blunt trauma are more insidious in onset, presenting as a painful pulsatile mass in the palmar area of the hand, and require prompt diagnosis and management to avoid catastrophic sequelae. Our case is the first study to describe a patient with traumatic PA of the palmar arch caused by blunt trauma that was treated with surgical reconstruction and venous bypass interposition.
2.Surgical Repair of a Giant Inferior Vena Cava Aneurysm Associated with a Congenital Vascular Anomaly: A Case Report
Konstantinos DIMITRIADIS ; Nikolaos PAPATHEODOROU ; Nikolaos TRIANTAFYLLOU ; Stavros PARISIDIS ; Christos ARGYRIOU ; George S. GEORGIADIS
Vascular Specialist International 2024;40(4):42-
Inferior vena cava aneurysms (IVCAs) are rare yet potentially lethal, especially if they are symptomatic or complicated. Among the IVCAs reported in the literature, only a few are associated with congenital vascular anomalies, including congenital IVC obstruction, tetralogy of Fallot, left-sided IVC, duplicated IVC, Ehlers–Danlos syndrome, blue rubber bleb nevus syndrome, and Klipper-Trenaunay syndrome.We present the case of an 8-cm symptomatic saccular IVCA in a patient with tetralogy of Fallot, treated successfully with surgical repair. Although rare venous pathologies can sometimes be managed with endovascular treatment, open surgical reconstruction remains the mainstay of durable and definitive repair.
3.Surgical Repair of a Giant Inferior Vena Cava Aneurysm Associated with a Congenital Vascular Anomaly: A Case Report
Konstantinos DIMITRIADIS ; Nikolaos PAPATHEODOROU ; Nikolaos TRIANTAFYLLOU ; Stavros PARISIDIS ; Christos ARGYRIOU ; George S. GEORGIADIS
Vascular Specialist International 2024;40(4):42-
Inferior vena cava aneurysms (IVCAs) are rare yet potentially lethal, especially if they are symptomatic or complicated. Among the IVCAs reported in the literature, only a few are associated with congenital vascular anomalies, including congenital IVC obstruction, tetralogy of Fallot, left-sided IVC, duplicated IVC, Ehlers–Danlos syndrome, blue rubber bleb nevus syndrome, and Klipper-Trenaunay syndrome.We present the case of an 8-cm symptomatic saccular IVCA in a patient with tetralogy of Fallot, treated successfully with surgical repair. Although rare venous pathologies can sometimes be managed with endovascular treatment, open surgical reconstruction remains the mainstay of durable and definitive repair.
4.Surgical Repair of a Giant Inferior Vena Cava Aneurysm Associated with a Congenital Vascular Anomaly: A Case Report
Konstantinos DIMITRIADIS ; Nikolaos PAPATHEODOROU ; Nikolaos TRIANTAFYLLOU ; Stavros PARISIDIS ; Christos ARGYRIOU ; George S. GEORGIADIS
Vascular Specialist International 2024;40(4):42-
Inferior vena cava aneurysms (IVCAs) are rare yet potentially lethal, especially if they are symptomatic or complicated. Among the IVCAs reported in the literature, only a few are associated with congenital vascular anomalies, including congenital IVC obstruction, tetralogy of Fallot, left-sided IVC, duplicated IVC, Ehlers–Danlos syndrome, blue rubber bleb nevus syndrome, and Klipper-Trenaunay syndrome.We present the case of an 8-cm symptomatic saccular IVCA in a patient with tetralogy of Fallot, treated successfully with surgical repair. Although rare venous pathologies can sometimes be managed with endovascular treatment, open surgical reconstruction remains the mainstay of durable and definitive repair.
5.Surgical Repair of a Giant Inferior Vena Cava Aneurysm Associated with a Congenital Vascular Anomaly: A Case Report
Konstantinos DIMITRIADIS ; Nikolaos PAPATHEODOROU ; Nikolaos TRIANTAFYLLOU ; Stavros PARISIDIS ; Christos ARGYRIOU ; George S. GEORGIADIS
Vascular Specialist International 2024;40(4):42-
Inferior vena cava aneurysms (IVCAs) are rare yet potentially lethal, especially if they are symptomatic or complicated. Among the IVCAs reported in the literature, only a few are associated with congenital vascular anomalies, including congenital IVC obstruction, tetralogy of Fallot, left-sided IVC, duplicated IVC, Ehlers–Danlos syndrome, blue rubber bleb nevus syndrome, and Klipper-Trenaunay syndrome.We present the case of an 8-cm symptomatic saccular IVCA in a patient with tetralogy of Fallot, treated successfully with surgical repair. Although rare venous pathologies can sometimes be managed with endovascular treatment, open surgical reconstruction remains the mainstay of durable and definitive repair.
6.Surgical Repair of a Giant Inferior Vena Cava Aneurysm Associated with a Congenital Vascular Anomaly: A Case Report
Konstantinos DIMITRIADIS ; Nikolaos PAPATHEODOROU ; Nikolaos TRIANTAFYLLOU ; Stavros PARISIDIS ; Christos ARGYRIOU ; George S. GEORGIADIS
Vascular Specialist International 2024;40(4):42-
Inferior vena cava aneurysms (IVCAs) are rare yet potentially lethal, especially if they are symptomatic or complicated. Among the IVCAs reported in the literature, only a few are associated with congenital vascular anomalies, including congenital IVC obstruction, tetralogy of Fallot, left-sided IVC, duplicated IVC, Ehlers–Danlos syndrome, blue rubber bleb nevus syndrome, and Klipper-Trenaunay syndrome.We present the case of an 8-cm symptomatic saccular IVCA in a patient with tetralogy of Fallot, treated successfully with surgical repair. Although rare venous pathologies can sometimes be managed with endovascular treatment, open surgical reconstruction remains the mainstay of durable and definitive repair.