Surgical treatment of hypothalamic hamartomas.


Journal

Neurosurgical review
ISSN: 1437-2320
Titre abrégé: Neurosurg Rev
Pays: Germany
ID NLM: 7908181

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 21 02 2020
accepted: 31 03 2020
revised: 29 03 2020
pubmed: 23 4 2020
medline: 16 6 2021
entrez: 23 4 2020
Statut: ppublish

Résumé

Hypothalamic hamartomas are aberrant masses, composed of abnormally distributed neurons and glia. Along endocrine and cognitive symptoms, they may cause epileptic seizures, including the specific gelastic and dacrystic seizures. Surgery is the treatment of drug-resistant hamartoma epilepsy, with associated positive results on endocrine, psychiatric, and cognitive symptoms. Recently, alternatives to open microsurgical treatment have been proposed. We review these techniques and compare their efficacy and safety. Open resection or disconnection of the hamartoma, either through pterional, transcallosal, or transventricular approach, leads to good epileptological control, but its high complication rate, up to 30%, limits its indications. The purely cisternal peduncular forms remain the only indication of open, pterional approach, while other strategies have been developed to overcome the neurological, endocrine, behavioral, or cognitive complications. Laser and radiofrequency thermocoagulation-based disconnection through robot-guided stereo-endoscopy has been proposed as an alternative to open microsurgical resection and stereotactic destruction. The goal is to allow safe and complete disconnection of a possibly complex attachment zone, through a single intraparenchymal trajectory which allows multiple laser or radiofrequency probe trajectory inside the ventricle. The efficacy was high, with 78% of favorable outcome, and the overall complication rate was 8%. It was especially effective in patients with isolated gelastic seizures and pure intraventricular hamartomas. Stereotactic radiosurgery has proved as efficacious and safer than open microsurgery, with around 60% of seizure control and a very low complication rate. Multiple stereotactic thermocoagulation showed very interesting results with 71% of seizure freedom and 2% of permanent complications. Stereotactic laser interstitial thermotherapy (LiTT) seems as effective as open microsurgery (from 76 to 81% of seizure freedom) but causes up to 20% of permanent complications. This technique has however been highly improved by targeting only the epileptogenic onset zone in the hamartoma, as shown on preoperative functional MRI, leading to an improvement of epilepsy control by 45% (92% of seizure freedom) with no postoperative morbidity. All these results suggest that the impact of the surgical procedure does not depend on purely technical matters (laser vs radiofrequency thermocoagulation or stereotactic vs robot-guided stereo-endoscopy) but relies on the understanding of the epileptic network, including inside the hamartoma, the aim being to plan an effective disconnection or lesion of the epileptogenic part while sparing the adjacent functional structures.

Identifiants

pubmed: 32318922
doi: 10.1007/s10143-020-01298-z
pii: 10.1007/s10143-020-01298-z
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

753-762

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Auteurs

Pierre Bourdillon (P)

Department of Neurosurgery, Rothschild Foundation Hospital, 29 Rue Manin, 75019, Paris, France. pierre.bourdillon@neurochirurgie.fr.
Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France. pierre.bourdillon@neurochirurgie.fr.
Sorbonne Université, Paris, France. pierre.bourdillon@neurochirurgie.fr.
INSERM U1127, CNRS, UMR7225, Brain and Spine Institute, Paris, France. pierre.bourdillon@neurochirurgie.fr.

S Ferrand-Sorbet (S)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

C Apra (C)

Sorbonne Université, Paris, France.
INSERM U1127, CNRS, UMR7225, Brain and Spine Institute, Paris, France.
Department of Neurosurgery, Pitié-Salpêtrière Hospital, Paris, France.

M Chipaux (M)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

E Raffo (E)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
Université de Lorraine, Nancy, France.

S Rosenberg (S)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

C Bulteau (C)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.
Université de Paris, Paris, France.

N Dorison (N)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

O Bekaert (O)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

V Dinkelacker (V)

Department of Neurology, Rothschild Foundation Hospital, Paris, France.

C Le Guérinel (C)

Department of Neurosurgery, Rothschild Foundation Hospital, 29 Rue Manin, 75019, Paris, France.

M Fohlen (M)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

G Dorfmüller (G)

Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.

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