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16 results on '"Cipri Claudia"'

1. Difficult Diagnosis and Management of Concealed Cushing

Author

Salcuni, Antonio Stefano, primary, Marchese, Francesca, additional, Cellini, Miriam, additional, Brunetti, Alessandro, additional, Kara, Elda, additional, Manso, Jacopo, additional, Tonelli, Veronica, additional, Cipri, Claudia, additional, Carpentieri, Maria, additional, Sciannimanico, Silvia Maria, additional, Galasso, Silvia, additional, Agus, Sandra, additional, and Vescini, Fabio, additional

Published
2024
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4. Una nuova complicanza del diabete: l’osteopatia

Author

Salcuni, Antonio Stefano, primary, Carpentieri, Maria, additional, Sciannimanico, Silvia Maria, additional, Galasso, Silvia, additional, Agus, Sandra, additional, Cipri, Claudia, additional, Cellini, Miriam, additional, and Vescini, Fabio, additional

Published
2021
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6. Abstract #185 Efficacy of 18F-Fluorocholine PET/ CT, 99MTC-MIBI Spect/CT and Highresolution Neck US in the Detection of Parathyroid Adenomas

Author

Grimaldi, Franco, primary, Kara, Elda, additional, Sciannimanico, Silvia Maria, additional, Cipri, Claudia, additional, Galasso, Silvia, additional, Carpentieri, Maria, additional, Vianello, Giampaolo, additional, Rensi, Marco, additional, Gregorio, Fernando Di, additional, and Vescini, Fabio, additional

Published
2019
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10. [ldquo]Hyperparanet[rdquo]: a multicenter Italian study on Primary Hyperparathyroidism

Author

Saponaro, Federica, primary, Cetani, Filomena, additional, Camozzi, Valentina, additional, D'Angelo, Antonella, additional, Minisola, Salvatore, additional, Scillitani, Alfredo, additional, Cipri, Claudia, additional, Palmieri, Serena, additional, Chiodini, Iacopo, additional, Romanelli, Francesco, additional, Madeo, Bruno, additional, Castellano, Elena, additional, Gianotti, Laura, additional, Faggiano, Antongiulio, additional, Cianferotti, Luisella, additional, Brandi, Maria Luisa, additional, Corbetta, Sabrina, additional, De, Feo Maria Laura, additional, Palermo, Andrea, additional, and Marcocci, Claudio, additional

Published
2017
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15. Thyroid function tests, incongruent internally and with thyroid status, both in a pregnant woman and in her newborn daughter

Author

D’Aurizio, Federica, Biasotto, Alessia, Cipri, Claudia, Grimaldi, Franco, Zucco, Jessica, Marzinotto, Stefania, Curcio, Francesco, and Benvenga, Salvatore

Abstract

Thyroid function tests (TFT) are extensively used in daily clinical practice. Here, we described a case of incongruent TFT both in a pregnant woman and in her newborn.A 32-year-old woman, diagnosed with autoimmune thyroiditis during her first pregnancy, was monitored during her second gestation. At week 5 + 2 days, thyroid-stimulating hormone (TSH) and free thyroxine (FT4) values (Dimension VISTA 1500, Siemens Healthineers) were within normal limits. At week 19 + 5 days, TSH remained normal while FT4 increased approximately by three-fold. FT4 inconsistency was with both TSH and the clinical status since she continued to be clinically euthyroid. On the same serum sample, thyroid autoantibodies were negative. At week 25 + 4 days, the patient complained of palpitations and dyspnea, with tachycardia. Even though TSH was normal, high levels of both FT4 and free triiodothyronine (FT3) were interpreted as evidence of thyroid overactivity and methimazole was started. TFT of the pregnant woman continued to be monitored throughout gestation. Postpartum FT4 and FT3 gradually returned to normal. TFT, performed on the daughter’s serum, 3 days after birth, showed the same inconsistency as her mother but without clinical signs of congenital hyperthyroidism. Based on the clinical and laboratory setting, the presence of circulating autoantibodies against T3 and T4 (THAb) was suspected and demonstrated by radioimmunoprecipitation.Analytical interferences should be supposed when TFT do not fit with the clinical picture and despite their infrequency, THAb must also be considered. To our knowledge, this is the first case describing the passage of THAb to the newborn.

Published
2022
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16. Acute suppurative thyroiditis caused by Gemella Morbillorum: a case report.

Author

Brunetti A, Cipri C, Sartor A, Bergamin-Bracale AM, Manso J, and Vescini F

Abstract

Background: Acute suppurative thyroiditis (AST) is a rare form of thyroid inflammation prevalently of bacterial origin, that usually affects subjects with risk factors such as immunodeficiency, sepsis, and neck fistulas. The most prevalent pathogens associated with AST are gram-positive aerobic bacteria, followed by gram-negatives, while infections by anaerobic germs are exceptionally rare. Gemella morbillorum is a facultative anaerobic gram-positive bacterium that commonly populates the upper respiratory tract. Infections by Gemella Morbillorum have been previously documented in different regions (ie. lung, brain, bone, liver), but never in the thyroid., Case Presentation: A 18-year-old male with no previous medical history presented to the emergency department complaining of a rapidly enlarging painful neck mass in left anterior latero-cervical region progressively worsening over the last two weeks, accompanied by dysphagia and fever. Blood tests showed the presence of thyroiditis (suppressed TSH with increased free thyroxine, elevated inflammation markers and neutrophilic leucocytosis). Neck ultrasonography and CT showed a large abscess involving the left thyroid lobe and extending to the ipsilateral laterocervical region, suggesting the diagnosis of AST. Prompt antibiotic therapy was started and subsequent surgical drainage of the abscess was performed, resulting in a rapid clinical recovery and in the restoration of normal thyroid function. The bacterial culture of the abscess showed exclusively the presence of Gemella morbillorum., Conclusion: We present the first documented case of AST caused by Gemella morbillorum in an otherwise healthy boy. Although rare, AST in immunocompetent patients is possible; prompt diagnosis and treatment of this condition is fundamental to avoid severe complications., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Published
2024
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