Outcome of Endoscopic Endonasal Surgery in Pediatric Craniopharyngiomas.


Journal

World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 27 08 2019
revised: 07 10 2019
accepted: 08 10 2019
pubmed: 21 10 2019
medline: 5 3 2020
entrez: 21 10 2019
Statut: ppublish

Résumé

In the last years, few reports have shown the feasibility of the endoscopic endonasal approach (EEA) for craniopharyngiomas in pediatric patients. For these tumors, recent studies have suggested less aggressive surgery, favoring the preservation of the patient's quality of life. The aim of this study was to assess the outcome of the EEA in a large series with specific attention on the long-term functional sequelae. All consecutive pediatric craniopharyngiomas operated on through this approach since 2000 were included in the study. Preoperative and postoperative operative clinical, radiologic, and pathologic features were retrieved from patient records (mean follow-up, 72 ± 67 months). The series included 25 patients (12 female; mean age, 8.9 ± 4.1 years). Most of the tumors presented with a supradiaphragmatic extension (88%). Removal was radical in 23 patients (92%). Complications consisted of 6 cerebrospinal fluid leaks (24%). One patient (4%) died of postoperative respiratory complications. Most patients (92%) developed panhypopituitarism and visual disturbances normalized or improved in 6 patients (43%). At follow-up, 9 patients (36%) were overweight/obese (6 were already overweight before surgery). The tumor recurrence rate was 19%. EEA can be an effective approach for midline craniopharyngiomas in children older than 3 years. It gives a satisfactory exposure of the suprasellar region and an adequate assessment of the brain-tumor interface. Its main limitations are age-related anatomic features of nasal/paranasal sinuses and the risk of cerebrospinal fluid leak.

Sections du résumé

BACKGROUND BACKGROUND
In the last years, few reports have shown the feasibility of the endoscopic endonasal approach (EEA) for craniopharyngiomas in pediatric patients. For these tumors, recent studies have suggested less aggressive surgery, favoring the preservation of the patient's quality of life.
OBJECTIVE OBJECTIVE
The aim of this study was to assess the outcome of the EEA in a large series with specific attention on the long-term functional sequelae.
MATERIALS METHODS
All consecutive pediatric craniopharyngiomas operated on through this approach since 2000 were included in the study. Preoperative and postoperative operative clinical, radiologic, and pathologic features were retrieved from patient records (mean follow-up, 72 ± 67 months).
RESULTS RESULTS
The series included 25 patients (12 female; mean age, 8.9 ± 4.1 years). Most of the tumors presented with a supradiaphragmatic extension (88%). Removal was radical in 23 patients (92%). Complications consisted of 6 cerebrospinal fluid leaks (24%). One patient (4%) died of postoperative respiratory complications. Most patients (92%) developed panhypopituitarism and visual disturbances normalized or improved in 6 patients (43%). At follow-up, 9 patients (36%) were overweight/obese (6 were already overweight before surgery). The tumor recurrence rate was 19%.
CONCLUSIONS CONCLUSIONS
EEA can be an effective approach for midline craniopharyngiomas in children older than 3 years. It gives a satisfactory exposure of the suprasellar region and an adequate assessment of the brain-tumor interface. Its main limitations are age-related anatomic features of nasal/paranasal sinuses and the risk of cerebrospinal fluid leak.

Identifiants

pubmed: 31629927
pii: S1878-8750(19)32654-3
doi: 10.1016/j.wneu.2019.10.039
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e277-e288

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Diego Mazzatenta (D)

Center for Diagnosis and Treatment of Pituitary and Skull Base Tumors (Pituitary Unit), IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

Matteo Zoli (M)

Center for Diagnosis and Treatment of Pituitary and Skull Base Tumors (Pituitary Unit), IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy. Electronic address: matteo.zoli4@unibo.it.

Federica Guaraldi (F)

Center for Diagnosis and Treatment of Pituitary and Skull Base Tumors (Pituitary Unit), IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

Francesca Ambrosi (F)

Department of Biomedical and Neuromuscular Sciences, Section of Anatomic Pathology "M. Malpighi" at Bellaria Hospital, University of Bologna, Bologna, Italy.

Marco Faustini Fustini (M)

Center for Diagnosis and Treatment of Pituitary and Skull Base Tumors (Pituitary Unit), IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.

Ernesto Pasquini (E)

Department of Ear Nose and Throat Diseases, Bellaria Hospital, Bologna, Italy.

Sofia Asioli (S)

Department of Biomedical and Neuromuscular Sciences, Section of Anatomic Pathology "M. Malpighi" at Bellaria Hospital, University of Bologna, Bologna, Italy.

Mino Zucchelli (M)

Division of Pediatric Neurosurgery, Department of Neurosurgery, Bellaria Hospital, Bologna, Italy.

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