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Department of Endocrinology, Metabolism and Diabetes, Evgenideion Hospital, Athens University School of Medicine, Athens, Greece
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, Patel A, Hoperia V, Bauer A, Burman KD, Wartofsky L, Vasko V: Metformin inhibits growth and decreases resistance to anoikis in medullary thyroid cancer cells. Endocr Relat Cancer 2012;19:447-456. 10.1530/ERC-12-0046 22389381 37 Andrade BM, Araujo
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Fleury Medicine and Health, São Paulo, Brazil
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Fleury Medicine and Health, São Paulo, Brazil
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Fleury Medicine and Health, São Paulo, Brazil
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Fleury Medicine and Health, São Paulo, Brazil
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Introduction Serum calcitonin (sCT) is a useful biomarker for medullary thyroid cancer (MTC) and is employed for its diagnosis and follow-up monitoring [ 1 ]. In addition, some guidelines advocate sCT measurements for the differential
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Discovery In the absence of a history of external beam radiation or familial medullary thyroid cancer, the risk of malignancy in thyroid incidentalomas diagnosed on neck US, CT or MRI is 5-13% [ 11 , 14 ]. In contrast, the risk of malignancy when diagnosed
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Introduction Thyroid C cells representing the second endocrine cell type of the gland nowadays gain interest mainly as the origin of medullary thyroid cancer (MTC), which despite an often indolent local growth is an invasive and metastatic
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Introduction Calcitonin (CT), a 32-amino acid calcium-lowering peptide secreted by the C-cells (parafollicular cells) of the thyroid, is used as a marker for the diagnosis and the follow-up of medullary thyroid cancer (MTC) [ 1 ]. In patients
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annotations, markings, writings, or crosshairs within the nodule were excluded. Multinodular goiters without a separable nodule on the ultrasound image, medullary thyroid cancer, metastasis from other cancers, thyroid lymphomas, and purely cystic nodules were
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Introduction: This study aimed at comparing thyroid cancer staging when taking into account the differences between the “T” assessment” using ultrasound (US) and histopathological measurements. Material and Methods: This retrospective study included all consecutive differentiated follicular thyroid cancer (DTC) and medullary thyroid cancer (MTC) patients who underwent postoperative histopathological staging assessment at a single institution. Anaplastic thyroid carcinomas were excluded from the present study. Each malignant thyroid nodule was precisely evaluated by measuring its long axis using both US and gross specimen histopathological examination. T stage classification was attributed to each tumor as regards US (solely according to the tumor dimension) and histopathology: (1) solely according to the tumor dimension and (2) according to the tumor dimension and extrathyroidal extension features when present. Results: Retrospective comparison between US and histopathology size of the operated thyroid nodules showed a mean diminution of 7.52% of the tumor long axis. Tumors ≤10 mm at histopathological examination showed a larger decrease in size of 13% (p = 0.054, statistically significant) compared to the US measurements. Ten out of 72 (13.8%) patients showed final T downstaging in comparison to US assessment: (US) T2 to T1b in 6 patients (1 MTC) and (US) T1b to T1a in 4 patients (1 MTC). Two (2.9%) DTC patients were downstaged from stage 2 to stage 1. Conclusion: Precise thyroid tumor US measurement may differ significantly from that obtained by histopathological assessment, which may result in a different TNM staging and subsequent patient management.
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Neurofibromatosis Expert Team, Maastricht University Medical Centre, Maastricht, The Netherlands
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Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands
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Department of Radiology and Nuclear Medicine, Maastricht University Medical Centre, Maastricht, The Netherlands
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Purpose: To investigate thyroid gland characteristics on <sup>18</sup>F-FDG positron emission tomography/computed tomography (PET/CT) imaging in patients with neurofibromatosis type 1 (NF1). Subjects and Methods: Thyroid gland characteristics of patients with a clinical diagnosis of NF1 who underwent <sup>18</sup>F-FDG PET/CT imaging for the first time to distinguish benign neurofibroma from malignant peripheral nerve sheath tumor (MPNST) at our institution (n = 69) were compared to PET/CT imaging of sarcoidosis (n = 25) and early stage lung cancer (T<sub>1</sub>N<sub>0</sub>M<sub>0</sub> tumors, n = 15) patients. Results: Two NF1 patients (3%) showed a diffuse <sup>18</sup>F-FDG<sup></sup> uptake in the thyroid gland, 2 patients (3%) had an irregular uptake, and 7 patients (10%) had a focal uptake. Among the sarcoidosis patients, 1 showed a diffuse uptake (4%) and 1 had an irregular uptake (4%). In the early stage lung cancer group, 1 patient showed a diffuse uptake (7%) and 1 had a focal uptake (7%). NF1 patients had larger mean thyroid volume and mean SUV<sub>max</sub> compared to sarcoidosis patients but not compared to early stage lung cancer patients. Four NF1 patients were diagnosed with multinodular goiter, 2 patients were diagnosed with benign chronic lymphocytic thyroiditis, 1 patient had metastasis to the thyroid, and 1 patient had medullary thyroid cancer. Conclusion: Even though NF1 patients did not show an increased risk of thyroid incidentaloma on PET/CT compared to previous studies on non-thyroid cancer patients, the incidence shows that awareness of possible thyroid disease is important.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway
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Department of Pathology, Haukeland University Hospital Bergen, Bergen, Norway
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Department of Medical Genetics, St. Olavs University Hospital, Trondheim, Norway
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Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway
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1050-7256 4 Pelizzo MR , Boschin IM , Bernante P , Toniato A , Piotto A , Pagetta C , et al. Natural history, diagnosis, treatment and outcome of medullary thyroid cancer: 37 years experience on 157 patients . Eur J Surg Oncol
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Task Force, Kloos RT, Eng C, Evans DB, Francis GL, Gagel RF, Gharib H, Moley JF, Pacini F, Ringel MD, Schlumberger M, Wells SA Jr: Medullary thyroid cancer: management guidelines of the American Thyroid Association. Thyroid 2009;19:565-612. 10.1089/thy