Vascular malformation rupture in a patient affected by Costello syndrome.
Francesca BarbieriIgnacio Fernando HallLeonardo EliaEfrem CiviliniPublished in: BMJ case reports (2022)
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.
Keyphrases
- case report
- genome wide
- liver failure
- end stage renal disease
- signaling pathway
- genome wide identification
- oxidative stress
- ejection fraction
- respiratory failure
- coronary artery
- chronic kidney disease
- endothelial cells
- dna methylation
- prognostic factors
- copy number
- peritoneal dialysis
- aortic dissection
- transcription factor
- pi k akt
- mass spectrometry
- patient reported outcomes
- wild type
- acute respiratory distress syndrome
- genome wide analysis
- mechanical ventilation
- ultrasound guided
- optical coherence tomography