Visualizing protoporphyrin IX formation in the dura tail of meningiomas by mass spectrometry imaging
Benjamin Brokinkel1, Sabrina Kröger2, Volker Senner3
1Department of Neurosurgery, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, North Rhine-Westphalia, Germany. benjamin.brokinkel@ukmuenster.de.
Background:
The advantages of 5-aminolevulinacid (5-ALA)-induced fluorescence-guided surgery in meningiomas are increasingly discussed. In this context, despite detectable tumor tissue in histopathologial analyses, no fluorescence was shown at the dura tail using the standard operating microscope. Thus, 5-ALA metabolism in this surgically important site remains unknown but needs to be elucidated when further evaluating indications of fluorescence-guided surgery in meningiomas.
Method:
We here present the spatially resolved identification of protoporphyrin IX (PpIX) in sphenoid ridge meningioma cryosections from a patient who underwent fluorescence-guided microsurgery using molecular imaging analysis by matrix-assisted laser desorption/ionization tandem mass spectrometry (MALDI-MS/MS).
Results:
Despite a strong fluorescence of the main tumor, no fluorescence could be detected at the dura tail using the standard operating microscope (blue-light, 405 nm). However, histopathological analyses clearly showed meningioma tissue. Remarkably, MALDI-MS/MS analysis revealed PpIX formation also at the non-fluorescing dura tail. However, no PpIX was detected in the tumor free dura mater.
Conclusion:
MALDI-MS/MS visualized a selective accumulation of PpIX within the tumor tissue including the dura tail. Thus, absence of fluorescence in the dura tail as visualized by the operating microscope is not caused by the lack of PpIX formation.
Insights
5-aminolevulinic acid (5-ALA) fluorescence-guided surgery for meningiomas shows tumor tissue in the dura tail without visible fluorescence. Molecular imaging reveals protoporphyrin IX (PpIX) formation in the dura tail, indicating fluorescence absence is not due to lack of PpIX.
Area of Science:
- Neurosurgery
- Oncology
- Molecular Imaging
Background:
- 5-aminolevulinic acid (5-ALA) fluorescence-guided surgery (FGS) is increasingly used for meningiomas.
- Tumor tissue in the dura tail may not fluoresce under standard microscopy despite histopathological confirmation.
- Understanding 5-ALA metabolism in the dura tail is crucial for FGS in meningiomas.
Purpose of the Study:
- To investigate the presence and distribution of protoporphyrin IX (PpIX) in sphenoid ridge meningioma, specifically in the dura tail.
- To correlate fluorescence observed during surgery with molecular imaging findings.
Main Methods:
- Spatially resolved molecular imaging analysis using matrix-assisted laser desorption/ionization tandem mass spectrometry (MALDI-MS/MS).
- Analysis of cryosections from sphenoid ridge meningioma, including the dura tail.
- Comparison of MALDI-MS/MS findings with standard operating microscope visualization.
Main Results:
- Despite no visible fluorescence at the dura tail under the operating microscope, histopathology confirmed meningioma tissue.
- MALDI-MS/MS detected protoporphyrin IX (PpIX) formation in the non-fluorescing dura tail.
- PpIX was selectively accumulated in tumor tissue, including the dura tail, but not in tumor-free dura mater.
Conclusions:
- The absence of fluorescence in the dura tail during 5-ALA FGS is not due to a lack of PpIX formation.
- MALDI-MS/MS imaging reveals PpIX accumulation in the dura tail, suggesting potential for FGS in this region.
- Further evaluation of FGS indications in meningiomas should consider these molecular imaging findings.
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