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Oncocytic Features in Choroid Plexus Tumors: An Integrative Clinicopathological Study
Eliezer Villanueva-Castro1, Marco Antonio Muñuzuri-Camacho1, Martha Lilia Tena-Suck2
1Neurosurgery, National Institute of Neurology and Neurosurgery Manuel Velasco Suárez, Mexico City, MEX.
Oncocytic changes (OCs) in choroid plexus tumors (CPTs) are rare but linked to increased mortality and specific cellular markers. These OCs may indicate inflammatory responses and ciliary dysfunction in brain tumors.
Area of Science:
- Neuro-oncology
- Cellular biology
- Tumor pathology
Background:
- Choroid plexus tumors (CPTs) are rare brain neoplasms.
- Limited understanding of oncocytic changes (OCs) and amyloid in CPTs.
Purpose of the Study:
- Investigate the occurrence and biological significance of OCs in CPTs.
- Correlate OCs with clinicopathological features and patient outcomes.
Main Methods:
- Analysis of 42 primary and recurrent CPTs (WHO 2021 classification).
- Histopathological examination for OCs, amyloid, and other features.
- Immunohistochemical staining for various markers (fascin, CD1a, interleukins, TNF-α, HIF-1α).
Main Results:
- OCs observed in 36% of CPP, 38% of ACPP, and 17% of CPC.
- OCs correlated with mortality (p=0.049), necrosis (p=0.014), and hemorrhage (p=0.000).
- Positive reactions for fascin, CD1a, IL-2, IL-6, TNF-α, CD68, and HIF-1α; epithelial cells in CPP/CPC did not react.
Conclusions:
- OCs in CPTs are rare, associated with inflammatory, ischemic, and hypoxic conditions.
- OCs may involve dendritic cells and are linked to ciliary dysfunction.
- Further research is needed to elucidate the role of OCs in CPTs.
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