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The Utility of F-18 DOPA PET/CT in Identifying Unknown Primary Site of Neuroendocrine Disease

The Utility of F-18 DOPA PET/CT in Identifying Unknown Primary Site of Neuroendocrine Disease. Damita Thomas MD1, Yusuf Menda MD1, David Bushnell MD3 Thomas O’Dorisio MD2

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The Utility of F-18 DOPA PET/CT in Identifying Unknown Primary Site of Neuroendocrine Disease

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  1. The Utility of F-18 DOPA PET/CT in Identifying Unknown Primary Site of Neuroendocrine Disease Damita Thomas MD1, Yusuf Menda MD1, David Bushnell MD3 Thomas O’Dorisio MD2 1 University of Iowa Hospitals and Clinics Division of Nuclear Medicine 2 University of Iowa Hospitals and Clinics Division of Endocrinology 3 Veterans’ Administration Medical Center, Iowa City Results The primary site of disease was not identified in any of the 12 patients by any of the imaging modalities. Although F-18 DOPA PET/CT did show a suspicious lesion in the pancreatic head in one patient, CT nor endoscopic ultrasound revealed an anatomical correlate to further pursue. It also appeared that contrast enhanced CT detected more metastatic bone, liver, and retroperitoneal lymphadenopathy lesions with better distinction than unenhanced F-18 DOPA PET/CT. Introduction Several studies have shown that positron emission tomography with F-18 fluoro-dihydroxyphenylalanine has been useful in the initial diagnosis, staging, and restaging of neuroendocrine disease. However, little is known about its efficacy in locating the unknown primary site of NET disease in patients with known metastases or a biochemical profile highly suggestive of NET. Methods/Patients Twelve consecutive patients with a history of biopsy-proven primary carcinoid tumor that had previously been resected with recurrence of symptoms (n=2), metastatic carcinoid disease with an unknown primary site of disease (n=3), or a symptom complex with biochemical markers highly suspicious for a neuroendocrine tumor (either carcinoid n=5, or pheochromocytoma n=2) were evaluated. All patients underwent F-18 DOPA PET/CT scans after undergoing CT and/or MRI, Indium-111 pentetreotide scintigraphy, and I-123 metaiodobenzylguanidine (I-123 MIBG) imaging (specifically in the two patients with suspected pheochromocytoma). All patients received clinical follow up after all imaging modalities were completed. Purpose To determine if F-18 DOPA PET/CT could identify the primary site of NET in a series of 12 patients with biopsy proven NET metastases or a clinical syndrome suggestive of NET where other imaging modalities failed to. Conclusion Although F-18 DOPA PET/CT has been shown by others to be useful in characterizing the disease extent in patients with known neuroendocrine tumors, our experience shows that it may be less useful in determining the primary site of disease.

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