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18F-FDG Uptake in a T2 Hypointense Paraspinal Mass
Aparna Singhal1, Narendra Adhikari1, Diego A de Idiaquez Bakula2
1From the Section of Neuroradiology, Department of Radiology.
A rare spinal amyloidoma was incidentally discovered in a 77-year-old man during lymphoma evaluation using F-FDG PET/CT. Biopsy confirmed amyloidoma, distinguishing it from lymphoma despite initial FDG uptake.
Area of Science:
- Neurology
- Pathology
- Radiology
Background:
- Spinal tumors are rare, and paraspinal masses require careful differential diagnosis.
- Amyloidomas are uncommon localized amyloid deposits, rarely presenting in the spine.
- Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (F-FDG PET/CT) is utilized for cancer staging and evaluation.
Observation:
- A solitary, F-FDG avid lesion was incidentally identified in the T11-T12 paraspinal region of a 77-year-old male patient.
- Magnetic Resonance Imaging (MRI) revealed a lesion with T2 hypointensity and contrast enhancement.
- Initial suspicion leaned towards lymphoma due to the lesion's F-FDG avidity.
Findings:
- Histopathological examination via biopsy was crucial for definitive diagnosis.
- Biopsy demonstrated nodules of extracellular, acellular, homogeneous material.
- Congo red staining exhibited characteristic apple-green birefringence, confirming amyloidoma.
Implications:
- This case highlights the importance of histopathological confirmation for paraspinal masses, even with high F-FDG uptake.
- Spinal amyloidoma is a rare entity that can mimic malignant lesions on imaging.
- Accurate diagnosis of spinal amyloidoma is essential for appropriate patient management and prognosis.
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