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Published on: September 27, 2013
Neurosurgical Flexible Probe Microscopy with Enhanced Architectural and Cytological Detail
Hany Osman1, Deena Elsahy2, Veronika Slivova3
1Wellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Background:
Microscopic delineation and clearance of tumor cells at neurosurgical excision margins potentially reduce tumor recurrence and increase patient survival. Probe-based in vivo fluorescence microscopy technologies are promising for neurosurgical in vivo microscopy.
Objective:
We sought to demonstrate a flexible fiberoptic epifluorescence microscope capable of enhanced architectural and cytological imaging for in vivo microscopy during neurosurgical procedures.
Methods:
Eighteen specimens were procured from neurosurgical procedures. These specimens were stained with acridine orange and imaged with a 3-dimensional (3D)-printed epifluorescent microscope that incorporates a flexible fiberoptic probe. Still images and video sequence frames were processed using frame alignment, signal projection, and pseudo-coloring, resulting in resolution enhancement and an increased field of view.
Results:
Images produced displayed good nuclear contrast and architectural detail. Grade 1 meningiomas demonstrated 3D chords and whorls. Low-grade meningothelial nuclei showed streaming and displayed regularity in size, shape, and distribution. Oligodendrogliomas showed regular round nuclei and a variably staining background. Glioblastomas showed high degrees of nuclear pleomorphism and disarray. Mitoses, vascular proliferation, and necrosis were evident.
Conclusions:
We demonstrate the utility of a 3D-printed, flexible probe microscope for high-resolution microscopic imaging with increased architectural detail. Enhanced in vivo imaging using this device may improve our ability to detect and decrease microscopic tumor burden at excision margins during neurosurgical procedures.
Insights
A new 3D-printed microscope with a flexible probe enhances in vivo neurosurgical imaging. This technology improves visualization of tumor cells at excision margins, potentially reducing recurrence and improving patient survival.
Area of Science:
- Neurosurgery
- Medical Imaging
- Biotechnology
Background:
- Accurate tumor cell clearance at surgical margins is crucial for reducing recurrence and improving survival in neurosurgery.
- In vivo fluorescence microscopy offers promising advancements for real-time intraoperative visualization.
- Existing technologies require enhancement for detailed cellular and architectural imaging during procedures.
Purpose of the Study:
- To develop and demonstrate a flexible fiberoptic epifluorescence microscope for enhanced in vivo neurosurgical imaging.
- To achieve superior architectural and cytological detail during live surgical procedures.
Main Methods:
- Procurement of 18 neurosurgical specimens.
- Staining with acridine orange and imaging using a 3D-printed epifluorescent microscope with a flexible fiberoptic probe.
- Image processing including frame alignment, signal projection, and pseudo-coloring for resolution and field-of-view enhancement.
Main Results:
- The microscope produced images with excellent nuclear contrast and detailed architecture.
- Specific tumor types like meningiomas and oligodendrogliomas showed characteristic cellular patterns.
- High-grade tumors like glioblastomas exhibited significant nuclear pleomorphism and disarray, with visible mitoses and vascular proliferation.
Conclusions:
- A 3D-printed, flexible probe microscope enables high-resolution in vivo microscopic imaging with enhanced architectural detail.
- This advanced imaging capability can improve the detection and clearance of microscopic tumor burdens at surgical margins.
- The technology holds potential to enhance neurosurgical outcomes by improving precision in tumor resection.
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