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mechanical ventilation was introduced, but despite intensive treatment, he died 4 h after admission. The body underwent autopsy which showed acute respiratory distress syndrome as a cause of death. Besides, samples of thyroid gland obtained from the deceased
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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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. Table 1. Overview of the current literature on NF1 with concurrent thyroid disease This study analyses thyroid gland abnormalities in a population of NF1 patients who underwent 18 F-FDG PET/CT. We selected 2 other non-thyroid cancer patient
Department of Radiology, Jichi Medical University, School of Medicine, Shimotsuke, Tochigi, Japan
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Center for Frontier Medical Engineering, Chiba University, Yayoicho, Inage–ku, Chiba, Japan
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Introduction Abnormal 18F–fluorodeoxyglucose (FDG) accumulation in the thyroid gland is observed in 5% of patients ( 1 , 2 , 3 ). The standardized uptake value (SUV) and pattern of accumulation (focal, diffuse, and diffuse-plus-focal) are
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cases, a definite treatment protocol has not been established for the management of this pathology. What Does This Case Report Add? This case report presents the 13 cases of liposarcoma of the thyroid gland described in the literature
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Department of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, Athens, Greece
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the thymus gland. MALT lymphoma of the thyroid gland is rarely reported in the literature as its incidence is significantly lower than that of other organs [ 1 , 2 ]. Compared to diffuse large B-cell lymphoma (DLBCL), MALT lymphoma is less
Department of Paediatrics, Southport and Ormskirk NHS Trust, Ormskirk, United Kingdom
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associated with an increased risk of disability [ 1 - 3 ]. Factors that may contribute to abnormal thyroid function in preterm infants include immaturity of the thyroid gland, disruption of maternal transfer of thyroid hormones through the placenta, and
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Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan
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gland has been rarely reported as one of the primary sites of MTX-associated LPDs (MTX-LPDs) [ 1 - 4 ]. Of note, there is little information regarding the sonographic characteristics of MTX-LPD of the thyroid gland and its natural course following MTX
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NOVA Medical School/New University of Lisboa, Lisbon, Portugal
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symptoms. Novel Insights This is one of the few reported cases of diffuse lipomatosis with coexisting deposition of amyloid in the thyroid gland. Introduction Diffuse thyroid lipomatosis is a histopathological condition of
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ultrasonographers, using a TOSHIBA Aplio SSA-770A ultrasound system with PLT-1204AX (7-14 MHz) and PLT-805AT (5-12 MHz) linear probes. Surgical samples of the thyroid gland and lymph nodes were cut before fixation. Specimens were fixed in buffered formalin and
Department of Oto-Rhino-Laryngology – Head and Neck Surgery, University Hospital Essen, Essen, Germany
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Department of Ophthalmology, University Hospital Essen, Essen, Germany
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with the changes induced by the presurgical therapeutic intervention (e.g., Lugol) or antithyroid drug therapy. In human GD, the thyroid gland pathology is difficult to determine in early stages of disease due to lack of availability of the gland. An