Esthesioneuroblastoma: A Comprehensive Review of Diagnosis, Management, and Current Treatment Options.


Journal

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

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 15 11 2018
revised: 01 03 2019
accepted: 02 03 2019
pubmed: 14 3 2019
medline: 14 1 2020
entrez: 14 3 2019
Statut: ppublish

Résumé

Many controversies exist in the diagnosis and management of this aggressively malignant condition, mainly because of limited literature and lack of randomized control trials, resulting in nonstandardized treatment methods. We performed a comprehensive review of the literature to identify management approach and treatment options for esthesioneuroblastoma. An extensive review of the published literature was conducted in PubMed, OVID Medline, and EMBASE journals for studies of esthesioneuroblastoma. Terms for search included esthesioneuroblastoma (ENB) and olfactory neuroblastoma (ONB). No date restrictions were used. The search yielded 3876 related articles. Cross-checking of articles led to exclusion of duplicate articles. The remaining 1170 articles were screened for their full text and English language availability. Of 609 full-text articles available, animal studies, irrelevant articles, and studies with mixed/confusing data were excluded. We finalized 149 articles pertaining to the topic, including 119 original research articles, 3 book chapters, 11 reviews, 9 case reports, and 7 case series. Surgical resection followed by radiotherapy is the standard for treatment for higher-grade lesions. The endoscopic endonasal approach is gaining further recognition with more favorable outcomes and better survival than for open surgery. Postoperative radiotherapy is associated with the highest overall survival and shows benefit for patients with higher-stage disease and those who receive chemotherapy. Recurrence rates after treatment vary drastically in the literature and, therefore, prolonged follow-up with repeated imaging is recommended. Lifelong surveillance is recommended because of late recurrences associated with this tumor.

Identifiants

pubmed: 30862589
pii: S1878-8750(19)30627-8
doi: 10.1016/j.wneu.2019.03.014
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

194-211

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Brian Fiani (B)

Department of Neurosurgery, Desert Regional Medical Center, Palm Springs, California. Electronic address: bfiani@outlook.com.

Syed A Quadri (SA)

Department of Neurosurgery, Desert Regional Medical Center, Palm Springs, California; Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.

Alessandra Cathel (A)

Department of Neurosurgery, Desert Regional Medical Center, Palm Springs, California.

Mudassir Farooqui (M)

Department of Neurology, University of New Mexico, Albuquerque, New Mexico.

Anirudh Ramachandran (A)

College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California.

Imran Siddiqi (I)

College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California.

Hammad Ghanchi (H)

Department of Neurosurgery, Riverside University Health Systems, Moreno Valley, California, USA.

Atif Zafar (A)

Department of Neurology, University of New Mexico, Albuquerque, New Mexico.

Blake W Berman (BW)

Department of Neurosurgery, Desert Regional Medical Center, Palm Springs, California.

Javed Siddiqi (J)

Department of Neurosurgery, Desert Regional Medical Center, Palm Springs, California.

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Classifications MeSH