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Vascular malformation rupture in a patient affected by Costello syndrome

Articolo
Data di Pubblicazione:
2022
Abstract:
: Costello syndrome (CS) is a rare genetic syndrome affecting multiple organs, generally caused by mutations of the HRAS gene, belonging to the RAS/MAPK genes family.A male patient with CS developed a painful pulsatile mass on the lateral side of the wrist. An initial ultrasonographic investigation confirmed the presence of a radial artery lesion, possibly an arterial aneurysm. On surgical resection, histological evaluation showed a tangle of vascular structures with variable calibre and abnormal wall histology. Immunohistochemical stainings revealed a very poor endothelial contribution to the central vascular wall structure. These histological observations led us to conclude we had managed an acute vascular malformation (VM) rupture, rather than a common arterial aneurysmal condition. Considering the molecular mechanisms regulated by RAS/MAPK genes, CS patients might have a higher risk of developing VMs and, in the presence of a pulsatile mass with acute onset, VM rupture should be considered.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Cardiovascular medicine; Genetics; Vascular surgery
Elenco autori:
Barbieri, F.; Hall, I. F.; Elia, L.; Civilini, E.
Autori di Ateneo:
ELIA LEONARDO
Link alla scheda completa:
https://iris.unibs.it/handle/11379/568324
Pubblicato in:
BMJ CASE REPORT
Journal
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