Aneurysmal disease affecting the aorta and visceral vessels in young patients is uncommon and typically associated with connective tissue disorders. We describe the case of a 17-year-old girl who presented with acute onset of abdominal pain; computed tomography scan revealed aortic and bilateral renal artery aneurysms and a perirenal hematoma. She was taken to the angiography suite; rupture of the right renal artery aneurysm was identified and immediately treated successfully with coil embolization. The left renal artery aneurysm was repaired with ex-vivo renal autotransplantation; 2 years later, the aorta and right renal artery underwent surgical reconstruction
This report describes a patient with pseudoxanthoma elasticum (PXE) who presented with an incidental...
AbstractA 58-year-old woman with underlying medically controlled hypertension presented after an epi...
OBJECTIVE: Renal malformations are rare entities and rarely have clinical consequences. Crossed rena...
Aneurysmal disease affecting the aorta and visceral vessels in young patients is uncommon and typica...
AbstractArterial aneurysms in children are rare. When present, they are often associated with connec...
AbstractRenal artery aneurysms are rare and most are clinically silent until discovery. Indications ...
AbstractAlthough abdominal aortic aneurysm (AAA) is a common problem in elderly patients, AAA is rar...
AbstractA 6-year-old boy from China presented initially at 2 years of age with a pulsatile mass in h...
AbstractWe describe a case of a 36-year-old female patient who was investigated for renal artery ane...
Crossed fused renal ectopia in the presence of abdominal aortic aneurysms (AAAs) is a rare challenge...
Multiple major artery compression by an aortic aneurysm is extremely rare in the paediatric populati...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...
Loeys-Dietz syndrome is a recently described genetic connective tissue disorder. The syndrome is ass...
AbstractRenal artery fibromuscular dysplasia is a condition of unknown etiology, with non-inflammato...
Renal artery aneurysms are rare urologic conditions, with rupture being the most feared complication...
This report describes a patient with pseudoxanthoma elasticum (PXE) who presented with an incidental...
AbstractA 58-year-old woman with underlying medically controlled hypertension presented after an epi...
OBJECTIVE: Renal malformations are rare entities and rarely have clinical consequences. Crossed rena...
Aneurysmal disease affecting the aorta and visceral vessels in young patients is uncommon and typica...
AbstractArterial aneurysms in children are rare. When present, they are often associated with connec...
AbstractRenal artery aneurysms are rare and most are clinically silent until discovery. Indications ...
AbstractAlthough abdominal aortic aneurysm (AAA) is a common problem in elderly patients, AAA is rar...
AbstractA 6-year-old boy from China presented initially at 2 years of age with a pulsatile mass in h...
AbstractWe describe a case of a 36-year-old female patient who was investigated for renal artery ane...
Crossed fused renal ectopia in the presence of abdominal aortic aneurysms (AAAs) is a rare challenge...
Multiple major artery compression by an aortic aneurysm is extremely rare in the paediatric populati...
Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous syndrome, due to heterozygous pathoge...
Loeys-Dietz syndrome is a recently described genetic connective tissue disorder. The syndrome is ass...
AbstractRenal artery fibromuscular dysplasia is a condition of unknown etiology, with non-inflammato...
Renal artery aneurysms are rare urologic conditions, with rupture being the most feared complication...
This report describes a patient with pseudoxanthoma elasticum (PXE) who presented with an incidental...
AbstractA 58-year-old woman with underlying medically controlled hypertension presented after an epi...
OBJECTIVE: Renal malformations are rare entities and rarely have clinical consequences. Crossed rena...