Spinal Neurovascular Malformations in Klippel-Trenaunay Syndrome: A Single Center Study.


Journal

Neurosurgery
ISSN: 1524-4040
Titre abrégé: Neurosurgery
Pays: United States
ID NLM: 7802914

Informations de publication

Date de publication:
16 02 2021
Historique:
received: 15 04 2020
accepted: 08 08 2020
pubmed: 20 10 2020
medline: 5 5 2021
entrez: 19 10 2020
Statut: ppublish

Résumé

A number of studies have demonstrated spinal anomalies associated with Klippel-Trenaunay syndrome (KTS). To date, there are no large consecutive series examining the prevalence and subtype distribution of spinal neurovascular malformations in patients with KTS. To report the spectrum and incidence of spinal neurovascular manifestations in the KTS population. This was a cross-sectional study. Consecutive patients with definite KTS as defined by International Society for the Study of Vascular Anomalies criteria who underwent spinal neuroimaging at our institution were included. All studies were evaluated by a staff neuroradiologist and a senior radiology resident for the presence of developmental venous anomalies, cavernous malformations (CMs), and arteriovenous shunts (AVS). A total of 116 patients with definite KTS who underwent spinal neuroimaging were included. A total of 23 neurovascular anomalies were found in 19 patients (16.4%), including 4 patients with multiple anomalies. These included 5 patients with spinal cord CMs (4.3%), 14 patients with a paraspinal or epidural venous malformation (12.1%), and 4 patients with an AVS (3.4%). Of the AVS, 3 were epidural arteriovenous fistulas, 1 of which likely formed de novo in an epidural venous malformation. One was a conus medullaris arteriovenous malformation. Our study cohort of 116 KTS patients demonstrated a wide spectrum of spinal neurovascular anomalies with a relatively high prevalence. Potential phenotypic descriptions of KTS should include the possibility for spinal neurovascular anomalies.

Sections du résumé

BACKGROUND
A number of studies have demonstrated spinal anomalies associated with Klippel-Trenaunay syndrome (KTS). To date, there are no large consecutive series examining the prevalence and subtype distribution of spinal neurovascular malformations in patients with KTS.
OBJECTIVE
To report the spectrum and incidence of spinal neurovascular manifestations in the KTS population.
METHODS
This was a cross-sectional study. Consecutive patients with definite KTS as defined by International Society for the Study of Vascular Anomalies criteria who underwent spinal neuroimaging at our institution were included. All studies were evaluated by a staff neuroradiologist and a senior radiology resident for the presence of developmental venous anomalies, cavernous malformations (CMs), and arteriovenous shunts (AVS).
RESULTS
A total of 116 patients with definite KTS who underwent spinal neuroimaging were included. A total of 23 neurovascular anomalies were found in 19 patients (16.4%), including 4 patients with multiple anomalies. These included 5 patients with spinal cord CMs (4.3%), 14 patients with a paraspinal or epidural venous malformation (12.1%), and 4 patients with an AVS (3.4%). Of the AVS, 3 were epidural arteriovenous fistulas, 1 of which likely formed de novo in an epidural venous malformation. One was a conus medullaris arteriovenous malformation.
CONCLUSION
Our study cohort of 116 KTS patients demonstrated a wide spectrum of spinal neurovascular anomalies with a relatively high prevalence. Potential phenotypic descriptions of KTS should include the possibility for spinal neurovascular anomalies.

Identifiants

pubmed: 33073841
pii: 5930279
doi: 10.1093/neuros/nyaa457
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

515-522

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 by the Congress of Neurological Surgeons.

Auteurs

Anthony Larson (A)

Department of Radiology, Mayo Clinic, Rochester, Minnesota.

Tristan Covington (T)

Department of Radiology, Mayo Clinic, Rochester, Minnesota.

Katelyn Anderson (K)

Department of Dermatology, Mayo Clinic, Rochester, Minnesota.

Megha Tollefson (M)

Department of Dermatology, Mayo Clinic, Rochester, Minnesota.

Giuseppe Lanzino (G)

Department of Radiology, Mayo Clinic, Rochester, Minnesota.
Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota.

Waleed Brinjikji (W)

Department of Radiology, Mayo Clinic, Rochester, Minnesota.
Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota.

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