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Véronique Raverot Hospices Civils de Lyon, Groupement Hospitalier Est, LBMMS, Centre de biologie et de pathologie Est, Lyon, France

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Stéphanie Metrat Hospices Civils de Lyon, Groupement Hospitalier Est, LBMMS, Centre de biologie et de pathologie Est, Lyon, France

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Pauline Perrin Hospices Civils de Lyon, Groupement Hospitalier Est, LBMMS, Centre de biologie et de pathologie Est, Lyon, France

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Juliette Abeillon Hospices Civils de Lyon, Groupement Hospitalier Est, Fédération d’Endocrinologie, Lyon, France

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Hélène Lasolle Hospices Civils de Lyon, Groupement Hospitalier Est, Fédération d’Endocrinologie, Lyon, France

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, inappropriate explorations and treatments. This observation adds to the literature as long-term evolution has been rarely studied ( 2 ). In the present case, biological abnormalities remained unchanged over time. Additionally, if case reports have described the

Article Type:
Case Report
Collections:
Thyroid function tests
DOI:
https://doi.org/10.1530/ETJ-24-0013
Volume/Issue:
Volume 13: Issue 3
Open access
Vittoria Guarda Department of Otolaryngology, Head and Neck Surgery, Technical University of Munich, Munich, Germany

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Anja Pickhard Department of Otolaryngology, Head and Neck Surgery, Technical University of Munich, Munich, Germany

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Melanie Boxberg Institute of Pathology, Technical University of Munich, Munich, Germany

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Katja Specht Institute of Pathology, Technical University of Munich, Munich, Germany

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Anna Maria Stefanie Buchberger Department of Otolaryngology, Head and Neck Surgery, Technical University of Munich, Munich, Germany

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What Is Known about This Topic? Liposarcomas of the thyroid gland are extremely rare, and there is no definitive consensus within the literature about a comprehensive treatment recommendation yet. What Does This Case Report Add

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000486333
Volume/Issue:
Volume 7: Issue 2
Free access
Darshan Patil Department of Surgical Oncology, HCG-Bangalore Institute of Oncology, Bangalore, India

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Abhay Kumaraswamy Kattepur Department of Surgical Oncology, HCG-Bangalore Institute of Oncology, Bangalore, India

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Srinivas Kodaganur Gopinath Department of Surgical Oncology, HCG-Bangalore Institute of Oncology, Bangalore, India

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Shivanand Swamy Department of Surgical Oncology, HCG-Bangalore Institute of Oncology, Bangalore, India

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Amarendra Shankarappa Department of Surgical Oncology, HCG-Bangalore Institute of Oncology, Bangalore, India

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Gopinath Kodaganur Srinivasachar Department of Surgical Oncology, HCG-Bangalore Institute of Oncology, Bangalore, India

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.1155/2011/735789 23198224 6 Munteanu M, Giuri S, Roæca C, Boruga O, Creåu O: Multifocal choroidal metastases from thyroid carcinoma: a case report. Chirurgia 2013;108:268-272. 23618581 7 Ferry AP, Font RL: Carcinoma metastatic to the eye and orbit: a clinic

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000360533
Volume/Issue:
Volume 3: Issue 2
Free access
Inês Damásio Endocrinology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Joana Simões-Pereira Endocrinology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Sara Donato Endocrinology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal
Nova Medical School, Lisbon, Portugal

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Mariana Horta Radiology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon Portugal

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Branca Maria Cavaco Molecular Pathobiology Research Unit (UIPM), Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Miguel Rito Pathology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Pedro Gomes Head and Neck Surgery Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Valeriano Leite Endocrinology Department, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal
Nova Medical School, Lisbon, Portugal

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resection of an ab initio unresectable tumor. Case report We report a case of a 51-year-old female patient, with a medical history of type 2 diabetes mellitus, obesity, and asthma, evaluated for the first time in our center in May 2021. She

Article Type:
Case Report
Collections:
Thyroid cancer - clinical
DOI:
https://doi.org/10.1530/ETJ-22-0179
Volume/Issue:
Volume 12: Issue 1
Open access
Marina Weber Pasa Thyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

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Rafael Selbach Scheffel Thyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

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André Borsatto Zanella Thyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

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Ana Luiza Maia Thyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

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José Miguel Dora Thyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

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. It was first described by Huang et al. [ 2 ], with several other CHS cases reported thereafter. Although CHS has been initially noted in neonates and children with vascular tumors, it is not restricted to this age group or type of tumor. The CHS

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000481253
Volume/Issue:
Volume 6: Issue 6
Free access
Daniela Rodrigues Cavaco Department of Endocrinology, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Ana Alves Rafael Department of General Surgery, CUF Academic Center – Hospital CUF Sintra and Hospital CUF Cascais, Lisbon, Portugal

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Rafael Cabrera Department of Pathology, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Helena Vilar Department of Endocrinology, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal

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Valeriano Leite Department of Endocrinology, Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal
NOVA Medical School/New University of Lisboa, Lisbon, Portugal

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,” and “thyrolipomatosis” in the PubMed, we could find only 39 case reports and only 6 also had concomitant amyloid deposition (Table  1 ). These patients usually presented with normal thyroid function and severe compressive symptoms [ 2 , 3 , 7 , 8

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000518444
Volume/Issue:
Volume 10: Issue 6
Free access
Christian Trummer Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria

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Hannes Reiher Department of Internal Medicine, Krankenhaus der Elisabethinen, Graz, Austria

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Verena Theiler-Schwetz Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria

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Marlene Pandis Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria

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Christian Gstettner Division of Nuclear Medicine, Department of Radiology, Medical University of Graz, Graz, Austria

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Peter Potzinger Department of Otorhinolaryngology, Krankenhaus der Elisabethinen, Graz, Austria

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Tilman Keck Department of Otorhinolaryngology, Krankenhaus der Elisabethinen, Graz, Austria

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Thomas R. Pieber Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria

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Sigurd Lax Department of Pathology, General Hospital Graz Sued-West, Graz, Austria
Institute of Pathology, Medical University of Graz, Graz, Austria
Institute for Clinical Pathology, Johannes Kepler University, Linz, Austria

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Johannes Haybaeck Department of Pathology, Medical Faculty, Otto-von-Guericke University Magdeburg, Magdeburg, Germany
Department of Neuropathology, Institute of Pathology, Medical University of Graz, Graz, Austria
Department of Pathology, Neuropathology and Molecular Pathology, Medical University of Innsbruck, Innsbruck, Austria

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Vinzenz Stepan Department of Internal Medicine, Krankenhaus der Elisabethinen, Graz, Austria

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Stefan Pilz Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria

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considered in the diagnostic process. Biochemical tests, family history, and functional as well as non-functional imaging studies may be helpful in establishing a diagnosis. What Does This Case Report Add? We present the very rare case

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000505020
Volume/Issue:
Volume 9: Issue 2
Free access
Akshay Khatri Division of Infectious Diseases, Department of Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell Health, Manhasset, New York, USA

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Esti Charlap Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell Health, Great Neck, New York, USA

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Angela Kim Division of Infectious Diseases, Department of Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell Health, Manhasset, New York, USA

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article, we report a patient diagnosed with subacute thyroiditis that was precipitated by COVID-19 infection. We also review the literature of similar cases. Case Report A 41-year-old Caucasian woman presented to the emergency room (ER) with

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000511872
Volume/Issue:
Volume 9: Issue 6
Free access
Ringo Manta Department of Nuclear Medicine, CHU Saint Pierre, Université Libre de Bruxelles (ULB), Brussels, Belgium

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Charlotte Martin Department of Infectious Diseases, CHU Saint Pierre, Université Libre de Bruxelles (ULB), Brussels, Belgium

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Vinciane Muls Department of Gastroenterology and Endoscopy, CHU Saint-Pierre, University Libre de Bruxelles (ULB), Brussels, Belgium

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Kris G Poppe Department of Endocrinology, CHU Saint Pierre, Université Libre de Bruxelles (ULB), Brussels, Belgium

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thyroid disorders ( 1 ). Case report A 22-year-old male was referred to our outpatient endocrinology clinic. The patient had a history of ulcerative colitis (UC) and nephrotic syndrome diagnosed in 2018 and 2020, respectively. He was treated with

Article Type:
Case Report
Collections:
Hyperthyroidism and thyrotoxicosis
DOI:
https://doi.org/10.1530/ETJ-22-0049
Volume/Issue:
Volume 11: Issue 4
Open access
Syed Mohd. Razi Department of Endocrinology, L.L.R.M. Medical College, Meerut

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Abhinav Kumar Gupta Department of Endocrinology, L.L.R.M. Medical College, Meerut

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Deepak Chand Gupta Department of Endocrinology, L.L.R.M. Medical College, Meerut

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Manish Gutch Department of Medicine, King George's Medical University, Lucknow

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Keshav Kumar Gupta Department of Endocrinology, L.L.R.M. Medical College, Meerut

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Syeda Iqra Usman Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India

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been described in the medical literature. What Does This Case Report Add? • This is the second description of the simultaneous occurrence of these rare syndromes, and we have shown that their manifestations fully resolve by thyroxine treatment

Article Type:
Case Report
DOI:
https://doi.org/10.1159/000448993
Volume/Issue:
Volume 6: Issue 1
Free access