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Vascular malformation rupture in a patient affected by Costello syndrome.
Barbieri, Francesca; Hall, Ignacio Fernando; Elia, Leonardo; Civilini, Efrem.
Afiliação
  • Barbieri F; Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy.
  • Hall IF; Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy.
  • Elia L; Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy leonardo.elia@unibs.it.
  • Civilini E; DMMT, Università degli Studi di Brescia, Brescia, Italy.
BMJ Case Rep ; 15(12)2022 Dec 16.
Article em En | MEDLINE | ID: mdl-36526283
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Cardiovasculares / Malformações Vasculares / Síndrome de Costello Limite: Humans / Male Idioma: En Revista: BMJ Case Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Cardiovasculares / Malformações Vasculares / Síndrome de Costello Limite: Humans / Male Idioma: En Revista: BMJ Case Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália