Literature DB >> 28922884

A Single-Institution Experience with Pineal Region Tumors: 50 Tumors Over 1 Decade.

Isaac Josh Abecassis1, Brian Hanak1, Jason Barber1, Martin Mortazavi1, Richard G Ellenbogen1.   

Abstract

BACKGROUND: Pineal region tumors are rare intracranial tumors that are more common in children than adults. Surgical management of tumors in this region using a tailored approach is a strategy that enhances extent of resection and neurological outcome.
OBJECTIVE: To review our institutional experience with pineal region tumors in children and adults over the past 10 years.
METHODS: Our institutional pathology database and patient records were retrospectively reviewed for details regarding clinical and radiological presentation, surgical management, extent of resection, morbidity, and neurological outcome. Statistical analysis was performed to assess for variables related to functional outcomes.
RESULTS: Fifty patients were identified as having undergone surgical management of a pineal region tumor with at least 1 year of follow-up. Forty-one percent presented with a Karnofsky Performance Scale (KPS) score of 70 or less, all of whom had concomitant hydrocephalus that required urgent treatment. The following variables were statistically significant to KPS score on admission: age, tumor volume, preoperative hydrocephalus, length of hospitalization (total and intensive care unit), and elevations in serum tumor markers. The median postoperative (2 months) KPS score was 90. The following variables were statistically significant with respect to change in KPS score postoperatively: tumor maximum diameter, KPS score on admission, and intensive care unit length of stay. The specific surgical strategy did not correlate to extent of tumor resection, morbidity, immediate neurological outcome, and progression-free survival.
CONCLUSION: Extent of resection, neurological outcome, and progression-free survival in the patients in our series were not related to the specific surgical approach employed and its perioperative complications.
Copyright © 2017 by the Congress of Neurological Surgeons

Entities:  

Keywords:  Biopsy; Pineal; Surgical approaches; Surgical outcomes; Tumors

Mesh:

Year:  2017        PMID: 28922884     DOI: 10.1093/ons/opx038

Source DB:  PubMed          Journal:  Oper Neurosurg (Hagerstown)        ISSN: 2332-4252            Impact factor:   2.703


  6 in total

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3.  Incidence, Prognostic Factors, and Survival Trend in Pineal Gland Tumors: A Population-Based Analysis.

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4.  Evaluation of the Perioperative and Postoperative Course of Surgery for Pineal Germinoma in the SIOP CNS GCT 96 Trial.

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5.  Treatment of Pineal Region Rosette-Forming Glioneuronal Tumors (RGNT).

Authors:  Anna Michel; Thiemo Florin Dinger; Ramazan Jabbarli; Philipp Dammann; Anne-Kathrin Uerschels; Marvin Darkwah Oppong; Neriman Özkan; Andreas Junker; Ulrich Sure; Karsten Henning Wrede
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6.  Retractorless interhemispheric transtentorial approach for large lesions in the posterior incisural space.

Authors:  Miguel Angel Lopez-Gonzalez; Andrew Jaeger; Brett Kaplan; Timothy Marc Eastin; Lydia Kore; Vadim Gospodarev; Puja D Patel; Fransua Sharafeddin
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  6 in total

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