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Calcifying pseudoneoplasms of the neuraxis (CAPNON). A case report
Wei-Qing Li1, Shen-Hao Wang2, Zheng-Wei Zhang1
1Department of Pathology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Summary
Calcifying pseudoneoplasms of the neuraxis (CAPNON) are rare brain lesions often misdiagnosed. This case highlights CAPNON
Area of Science:
- Neuropathology
- Neuroimaging
- Genetics
Background:
- Calcifying pseudoneoplasms of the neuraxis (CAPNON) are uncommon, benign lesions of the central nervous system.
- These lesions are frequently misdiagnosed due to their varied presentation and slow growth.
- Accurate diagnosis is crucial to avoid misclassification as neoplastic or infectious processes.
Observation:
- A 56-year-old woman presented with a six-year history of recurrent headaches.
- MRI revealed a 2.3 cm right frontal lobe mass with dense calcification, avid enhancement, and surrounding edema.
- Initial diagnosis was oligodendroglioma, but histopathology confirmed CAPNON.
Findings:
- Histopathological examination of the resected lesion was essential for definitive CAPNON diagnosis.
- Genetic analysis identified a nonsense mutation in the CUL4B gene.
- The observed condition was interpreted as a reactive process rather than a true neoplasm.
Implications:
- Increased awareness of CAPNON among clinicians is necessary to improve diagnostic accuracy.
- Histopathological confirmation is key to differentiating CAPNON from other intracranial pathologies.
- Avoiding unnecessary diagnostic workups and potentially harmful treatments for misdiagnosed CAPNON is critical.
Keywords:
CAPNONCUL4Bcalcifying pseudoneoplasm of the neuraxisnext-generation sequencingnonsense mutationMore Related Videos
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