Case report: Association between PTEN-gene variant and an aggressive case of multiple dAVFs.

AV fistulas PTEN gene mutation dural arteriovenous fistula (DAVF) gene variant pseudotumor cerebri

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2024
Historique:
received: 30 11 2023
accepted: 14 03 2024
medline: 23 4 2024
pubmed: 23 4 2024
entrez: 23 4 2024
Statut: epublish

Résumé

Mutations of the phosphatase and tensin homolog (PTEN) gene have been associated with a spectrum of disorders called PTEN hamartoma tumor syndrome, which predisposes the individual to develop various types of tumors and vascular anomalies. Its phenotypic spectrum includes Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), Proteus syndrome, autism spectrum disorders (ASD), some sporadic cancers, Lhermitte-Duclos disease (LDD), and various types of associated vascular anomalies. A previously healthy 27-year-old woman was experiencing visual scintillating scotomas and mild chronic headaches for the past 2 years. The initial computed tomographic (CT) and magnetic resonance imaging (MRI) scans did not reveal any abnormalities, but the possibility of pseudotumor cerebri was considered. Furthermore, a cerebral angiogram showed a posterior fossa dural arteriovenous fistula (dAVF), which was initially treated through embolization. However, in spite of proper treatment, this patient experienced multiple recurrent dAVFs in different locations, requiring multiple embolizations and surgeries. Despite exhibiting altered cerebral perfusion and hemodynamics, the patient did not display any significant symptoms until she experienced a sudden stroke resulting from deep venous thrombosis, which was not associated with any medical procedures or medication use. A comprehensive analysis was performed due to the aggressive nature of the dAVFs. Surprisingly, exome sequencing of a blood sample revealed a PTEN gene variant in chromosome 10, indicative of Cowden syndrome. However, no tumors or other vascular lesions were detected in other systems that would constitute Cowden syndrome. The rapid formation of multiple and complex dAVFs, coupled with not meeting the criteria for any other PTEN-related syndrome, unequivocally leads to the presentation of a novel phenotype of the PTEN germline variant.

Identifiants

pubmed: 38651102
doi: 10.3389/fneur.2024.1347289
pmc: PMC11033416
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1347289

Informations de copyright

Copyright © 2024 Jong-A-Liem, Sarti, dos Santos, Giacon, Wuo-Silva, Baeta, de Campos Filho and Chaddad-Neto.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Glaucia Suzanna Jong-A-Liem (GS)

Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Department of Neurosurgery, Hospital Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.

Talita Helena Martins Sarti (THM)

Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Department of Neurosurgery, Hospital Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.

Mariusi Glasenapp Dos Santos (MG)

Department of Neurosurgery, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.

Luciano Marcus Tirotti Giacon (LMT)

Department of Neuroradiology, Hospital Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.

Raphael Wuo-Silva (R)

Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, SP, Brazil.

Alex Machado Baeta (AM)

Department of Neurology, Hospital Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.

José Maria de Campos Filho (JM)

Department of Neurosurgery, Hospital Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.

Feres Chaddad-Neto (F)

Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Department of Neurosurgery, Hospital Beneficência Portuguesa de São Paulo, São Paulo, SP, Brazil.

Classifications MeSH