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Synapse vincent imaging system

Manufactured by Fujifilm
Sourced in Japan

The SYNAPSE VINCENT imaging system is a digital radiography solution designed for medical imaging applications. It provides high-quality digital images for diagnostic purposes. The system's core function is to capture and process radiographic images, enabling healthcare professionals to analyze and interpret patient data.

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2 protocols using synapse vincent imaging system

1

Volumetric Analysis of Skull Base Tumors

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The volumes of the whole tumor, the tumor located in the bilateral CS, and the bilateral LRSS were measured. All pre and postoperative MRI and preoperative computed tomography (CT) images were retrospectively reviewed by three authors (Kenzo Kosugi, Taro Mase, and Haruka Tamura), who calculated the whole tumor and CS tumor removal rate [Figure 1]. Volumetric analysis was performed using the SYNAPSE VINCENT imaging system (Fujifilm Medical Co., Tokyo, Japan), and the segmentation tool function was used on gadolinium-enhanced T1-weighted images obtained close to the surgery date. LRSS was examined using the coronal planes from each patient. On each coronal plane, the Vidian canal and the rotundum foramen were connected, and the SS area in the lateral line side was measured. The volume of both LRSS sides was calculated by integrating each area from end to end of the lateral recess in the coronal plane. The pre- and post-surgery volumes of the whole tumor volume and the bilateral CS tumor were also measured on the coronal plane.
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2

Endoscopic Endonasal Surgery for Pituitary Neuroendocrine Tumors

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A total of 106 patients with primary (new-onset) PitNETs who underwent surgery via EES from October 2012 to September 2022 at Keio University Hospital were retrospectively evaluated. The SYNAPSE VINCENT imaging system (Fujifilm Medical Co., Tokyo, Japan) was used for volumetric analysis. CS invasion was reported according to the Knosp criteria (13 (link)), and only those with Knosp grades 3 and 4 were included to evaluate the relationship between the lateral tumor extension and the simulation method used in the study. This study was approved by the Institutional Review Board (reference number: 20130379). Informed consent was obtained from all participants included in the study.
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