Department of Medicine, Thyroid Outpatient Clinic, Division of Endocrinology, Escola Paulista de Medicina, Universidade Federal de São Paulo, Sao Paulo, Brazil
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Lipid Clinic Heart Institute (InCor), University of Sao Paulo Medical School Hospital, Sao Paulo, Brazil
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School of Medicine, Faculdade Israelita de Ciências da Saúde Albert Einstein, Sao Paulo, Brazil
Center for Clinical and Epidemiological Research, University Hospital, University of São Paulo School of Medicine, Sao Paulo, Brazil
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disease (NAFLD) or non-alcoholic steatohepatitis [ 10 , 11 ]. In fact, NAFLD has long been recognized as the hepatic feature of the metabolic syndrome [ 12 ]. This condition may lead to hepatic fibrosis, cirrhosis, and hepatocellular carcinoma if not
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ectoderm [ 6 ]. MTCs comprise 4-8% of all thyroid cancers. Most cases are sporadic (75%). However, 25% are due to autosomal dominant inheritance as part of the MEN 2 syndrome or familial MTC. These inherited tumors are caused by germline point mutations
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of a distinct entity . Thyroid . 2011 Feb ; 21 ( 2 ): 135 – 44 . 10.1089/thy.2010.0226 21190448 1050-7256 8 Hall JE , Abdollahian DJ , Sinard RJ . Thyroid disease associated with Cowden syndrome: A meta-analysis . Head Neck
Department of Clinical Sciences and Community Health, University of Milan, Italy
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Department of Clinical Sciences and Community Health, University of Milan, Italy
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Department of Clinical Sciences and Community Health, University of Milan, Italy
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Introduction The pandemic of coronavirus disease 2019 (Covid-19), determined by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), originated in Wuhan (Hubei, China) in December 2019 and later spread worldwide ( 1 ). One of the
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Department of Human Genetics, McGill University, Montreal, Québec, Canada
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Department of Human Genetics, McGill University, Montreal, Québec, Canada
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, apart from MNG, it generally includes rare-to-very-rare entities [ 7 ]. DICER1 syndrome is caused by loss-of-function germline DICER1 alterations on chromosome 14q32.13 and exhibits an autosomal dominant pattern of inheritance [ 8 ]. Thyroid disease is
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Introduction The Marine-Lenhart syndrome (MLS), first described by Charkes in 1972 [ 1 ], is now commonly defined as “a combination of Graves’ disease and autonomous functioning thyroid nodule(s) (AFTN)” [ 2 - 4 ]. Typical scintigraphic images
Department of Medicine, King Chulalongkorn Memorial Hospital, Bangkok, Thailand
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Department of Preventive and Social Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
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Department of Preventive and Social Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
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hormones also have a role in hepatic lipid metabolism and hepatic insulin resistance [ 8 ]. Thyroid dysfunction can lead to hyperlipidemia, obesity, and insulin resistance, which are components of metabolic syndrome [ 9 ]. Given the hepatic manifestation
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What Is Known about This Topic? • New onset and exacerbation of autoimmune thyroid disease have been described after successful treatment of endogenous hypercortisolism. What Does This Case Report Add? • It seems that correction of
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What Is Known about This Topic? • Reported cases of hypertrophic osteoarthropathy (HOA) as a paraneoplastic syndrome associated with thyroid cancer are very rare. We report the first case of an unusual presentation of HOA and follicular
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Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands
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Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
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Department of Pediatric Radiology and Nuclear Medicine, Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
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Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands
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diagram of extensive literature results. Search strategy, Pubmed, search terms: (Cowden syndrome OR Cowden disease OR Bannayan Riley Ruvalcaba syndrome OR PTEN hamartoma syndrome) AND (thyroid cancer OR thyroid carcinoma OR thyroid nodule OR thyroid