Evidence map›Paper›PMID 41385139›Full record

ArticleNeurosurgical review2025

Endoscopic endonasal approach for rare sellar/parasellar pathologies: Insights from a neurosurgical perspective.

Atakan Emengen, Aykut Gökbel, Eren Yilmaz, Ayse Uzuner, Melih Caklili, Burak Cabuk, Ihsan Anik, Ozlem Yapıcıer, Savas Ceylan

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Article in Neurosurgical review, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Atakan EmengenDepartment of Neurosurgery, Pituitary Research Center, Bahcesehir University School of Medicine, Istanbul, Turkey.
Aykut GökbelDepartment of Neurosurgery, Istınye University School of Medicine, Istanbul, Turkey.
Eren YilmazDepartment of Neurosurgery, Istınye University School of Medicine, Istanbul, Turkey.
Ayse UzunerDepartment of Neurosurgery, Afsin State Hospital, Kahramanmaras, Turkey.
Melih CakliliDepartment of Neurosurgery, Kocaeli University School of Medicine, Kocaeli, Turkey.
Burak CabukDepartment of Neurosurgery, Kocaeli University School of Medicine, Kocaeli, Turkey.
Ihsan AnikDepartment of Neurosurgery, Kocaeli University School of Medicine, Kocaeli, Turkey.
Ozlem YapıcıerDepartment of Pathology, Bahcesehir University School of Medicine, Kocaeli, Turkey.
Savas CeylanDepartment of Neurosurgery, Pituitary Research Center, Bahcesehir University School of Medicine, Istanbul, Turkey. ssceylan@yahoo.com.ORCID http://orcid.org/0000-0002-2747-8907

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endoscopic endonasal approach (EEA) has become a well- established approach for skull base pathologies (SBP), providing a minimally invasive corridor to access various lesions. While the technique has been extensively studied for common skull base tumors, data on extremely rare pathologies remain limited. Our study aims to present our experience with rare SBPs managed via the EEA, highlighting the challenges associated with preoperative diagnosis, intraoperative decision-making, and surgical-strategy modifications. A retrospective analysis was conducted on patients who underwent endoscopic endonasal surgery at the tertiary center up to January 2025. Among 6,225 EEA performed, 41 patients with exceptionally rare SBP were identified. Each tumor type was separately evaluated for differences in resection, complication rates, and recurrence patterns. These included 6 pituitary pituicytomas, 5 plasmacytomas, 5 xanthogranulomas, 4 granular cell tumors, 3 giant cell tumors and others. Gross total resection was achieved in 68% of cases, with subtotal resection in vascular or malignant tumors. Intraoperative challenges included unexpected vascularity and fibrotic adhesions. Postoperative CSF leakage occurred in 7%, and recurrence was observed in 17%, mostly in malignant or partially resected tumors. No intraoperative mortality was recorded. Tailored adjuvant treatments ensured durable disease control in most patients. Even in highly experienced centers, rare SBP pose unique diagnostic and surgical challenges. The discrepancy between preoperative and intraoperative findings often necessitates real-time strategic adaptations. In these rare cases, for optimizing patient outcomes requires a comprehensive understanding of skull base anatomy, flexibility in surgical planning, readiness for sudden strategy modifications, and a multidisciplinary approach.

Indexed as

Natural Orifice Endoscopic SurgeryNeuroendoscopyNeurosurgical ProceduresPituitary NeoplasmsSella TurcicaSkull Base NeoplasmsAdolescentAdultAgedFemaleHumansMaleMiddle AgedNasal CavityPostoperative ComplicationsRetrospective StudiesEndoscopic endonasal approachPituicytomasPituitaryRare casesSkull baseXanthogranulomas

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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.