Evidence map›Paper›PMID 38592529›Full record

ReviewAdvances and technical standards in neurosurgery2024

Multimodal Approach for the Treatment of Complex Hypothalamic Hamartomas.

José Hinojosa, Santiago Candela-Cantó, Victoria Becerra, Jordi Muchart, Marta Gómez-Chiari, Jordi Rumia, Javier Aparicio

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances and technical standards in neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
3.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

José HinojosaDepartment of Neurosurgery, Hospital Sant Joan de Déu, Barcelona, Spain. jose.hinojosa@sjd.es.ORCID https://orcid.org/0000-0003-2438-7679
Santiago Candela-CantóDepartment of Neurosurgery, Hospital Sant Joan de Déu, Barcelona, Spain.ORCID https://orcid.org/0000-0002-7116-7727
Victoria BecerraDepartment of Neurosurgery, Hospital Sant Joan de Déu, Barcelona, Spain.
Jordi MuchartUnit for Epilepsy Surgery, Hospital Sant Joan de Déu, Barcelona, Spain.ORCID https://orcid.org/0000-0003-4702-5072
Marta Gómez-ChiariUnit for Epilepsy Surgery, Hospital Sant Joan de Déu, Barcelona, Spain.ORCID https://orcid.org/0000-0001-6726-1721
Jordi RumiaDepartment of Neurosurgery, Hospital Sant Joan de Déu, Barcelona, Spain.ORCID https://orcid.org/0000-0002-8755-8124
Javier AparicioUnit for Epilepsy Surgery, Hospital Sant Joan de Déu, Barcelona, Spain.ORCID https://orcid.org/0000-0002-2143-0953
Hospital Sant Joan de Déu Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypothalamic hamartomas (HHs) are rare congenital lesions formed by heterotopic neuronal and glial cells attached to the mammillary bodies, tuber cinereum, and hypothalamus.They often present with an intractable epilepsy typically characterized by gelastic seizures but commonly associated with other types of refractory seizures. The clinical course is progressive in most of the cases, starting with gelastic seizures in infancy and deteriorating into complex seizure disorders that result in catastrophic epilepsy associated with cognitive decline and behavioral disturbances.Hamartomas are known to be intrinsically epileptogenic and the site of origin for the gelastic seizures. As antiepileptic drugs are typically ineffective in controlling HH-related epilepsy, different surgical options have been proposed as a treatment to achieve seizure control. Resection or complete disconnection of the hamartoma from the mammillothalamic tract has proved to achieve a long-lasting control of the epileptic syndrome.Usually, symptoms and their severity are typically related to the size, localization, and type of attachment. Precocious puberty appears mostly in the pedunculated type, while epileptic syndrome and behavioral decline are frequently related to the sessile type. For this reason, different classifications of HHs have been developed based on their size, extension, and type of attachment to the hypothalamus.The bigger and more complex hypothalamic hamartomas typically present with severe refractory epilepsy, behavioral disturbances, and progressive cognitive decline posing a formidable challenge for the control of these symptoms.We present here our experience with the multimodal treatment for complex hypothalamic hamartomas. After an in-depth review of the literature, we systematize our approach for the different types of hypothalamic hamartomas.

Indexed as

Drug Resistant EpilepsyEpilepsies, PartialEpileptic SyndromesHamartomaHypothalamic DiseasesCombined Modality TherapyHumansGelastic seizuresHypothalamic hamartomaLaser interstitial thermal therapyMRgLITTPediatric epilepsyPrecocious pubertyRefractory epilepsy

Identifiers

PMID38592529
OpenAlexW4394626430

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.