An assessment of 18F-FDG PET/CT for thoracic screening and risk stratification of pulmonary nodules in multiple endocrine neoplasia type 1

<p><strong>Context:</strong> Bronchopulmonary neuroendocrine tumours (bpNETs) and thymic carci‐noid (ThC) are features of multiple endocrine neoplasia type 1 (MEN 1), and surveil‐lance guidelines recommend periodic thoracic imaging. The optimal thoracic imagingmodality and screening frequency remain uncertain as does the prognosis of smalllung nodules when identified.</p> <p><strong>Objectives:</strong> To evaluate fluorodeoxyglucose positron emission tomography/computed tomography (¹⁸F-FDG PET/CT) for identification and prognosticassessment of thoracic lesions in MEN 1.</p> <p><strong>Design:</strong> Retrospective observational study.</p> <p><strong>Setting and participants:</strong> Fifty consecutive MEN 1 patients undergoing screening with ¹⁸F-FDG PET/CT at a tertiary referral hospital between July 2011 and December 2016. </p><p><strong>Interventions:</strong> ¹⁸F-FDG PET/CT.</p> <p><strong>Outcome measures:</strong> Pulmonary and thymic lesion prevalence, size, functional characteristics and behaviour.</p> <p><strong>Results:</strong> Thirteen patients (26.0%) exhibited pulmonary nodules with multiple nod‐ules identified in nine (18.0%). An asymptomatic 31 mm FDG-avid ThC was identifiedin one patient (2%). Of the 13 patients with pulmonary nodules, four (8.0%) exhibited13 FDG-avid nodules (mean size 10.1 ± 9.1 mm), and nine (18.0%) demonstrated 26FDG nonavid nodules (mean size 6.9 ± 5.8 mm). All FDG-avid lesions increased in size vs 11 (42.3%) FDG nonavid lesions (<i>P</i> = .0004). For FDG-avid and nonavid nodules,the median doubling time was 24.2 months (IQR 11.4-40.7) and 48.6 months (IQR37.0-72.2), respectively. Nodule resection was undertaken in two patients, typicalbronchial carcinoid diagnosed in one (FDG nonavid) and metastatic renal cell carci‐noma in the second (FDG avid).</p> <p><strong>Conclusion:</strong> Thoracic imaging with ¹⁸F-FDG PET/CT effectively identifies pulmonary nodules and ThC. FDG-avid pulmonary lesions are significantly more likely to progress than nonavid lesions.</p>