Single dominant lesion in capillary malformation-arteriovenous malformation (CM-AVM) RASA1 syndrome.
Luis Fernando Sanchez-EspinoMarta IvarsCarolina Prat TorresCinzia E LavarinoNagore Gené OlacireguiCarlota Rovira ZurriagaVerónica P Celis PassiniMiguel Bejarano SerranoEulàlia BaselgaPublished in: Pediatric dermatology (2024)
We report two cases with localized vascular malformations clinically resembling the "dominant lesion" seen in capillary malformation-arteriovenous malformation (CM-AVM) syndrome, however, lacking germline RASA1 variants but presenting double somatic RASA1 variants in affected tissue. Both patients presented with localized and superficial high-flow vascular malformations were treated with surgery and laser therapy and showed partial resolution. The study underscores the rarity of somatic RASA1 variants, contributes to understanding the "second-hit" pathophysiology in vascular lesions, and emphasizes the significance of clinical distinctions and genotyping for accurate diagnoses, offering implications for diagnosis, prognosis, and genetic counseling.
Keyphrases
- copy number
- genome wide
- newly diagnosed
- end stage renal disease
- case report
- ejection fraction
- minimally invasive
- chronic kidney disease
- dna methylation
- prognostic factors
- high resolution
- high throughput
- oxidative stress
- dna repair
- acute coronary syndrome
- hepatitis c virus
- coronary artery disease
- human immunodeficiency virus
- single cell
- surgical site infection