Academic literature on the topic 'Autoimmune Adrenalitis'

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Journal articles on the topic "Autoimmune Adrenalitis"

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Min, Le, and Nageatte Ibrahim. "Ipilimumab-induced autoimmune adrenalitis." Lancet Diabetes & Endocrinology 1, no. 3 (2013): e15. http://dx.doi.org/10.1016/s2213-8587(13)70031-7.

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Chinnu, K. Antony* Navya Sunil Haritha B. Nair K. Menaka2 S. Haja Sherief T. Sivakumar. "ADDISON'S DISEASE- A CASE REPORT." Indo American Journal of Pharmaceutical Sciences 04, no. 12 (2017): 4198–200. https://doi.org/10.5281/zenodo.1095013.

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Addison ’s disease is a rare endocrine disease which is commonly due to autoimmune adrenalitis and tuberculosis. Usual manifestations involve chronic fatigue, muscle weakness, loss of appetite, nausea, vomiting, diarrhea, hypotension and hyper pigmentation of skin. A 64 year old female, presented with complaints of cough with expectoration, fever, breathlessness, darkening of skin and diarrhea. The treatment given for the patient was Inj. Dexamethasone for 4 days. Her symptoms resolved gradually after starting the therapy. Keywords: Addison’s disease, Cortisol, Autoimmune Adrenalit
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Frey, Felix J., Bernhard Trost, and Arthur Zimmermann. "Autoimmune Adrenalitis, Asthma and Membranoproliferative Glomerulonephritis." American Journal of Nephrology 11, no. 4 (1991): 341–42. http://dx.doi.org/10.1159/000168334.

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Silva, Omega L. "Isolated aldosterone deficiency and autoimmune adrenalitis." American Journal of Medicine 91, no. 2 (1991): 205. http://dx.doi.org/10.1016/0002-9343(91)90020-x.

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Nuralieva, Nurana F., Ekaterina A. Troshina, and Galina A. Melnichenko. "Lesions in endocrine glands as a complication of immunotherapy in the practice of oncologist." Clinical and experimental thyroidology 14, no. 4 (2019): 174–82. http://dx.doi.org/10.14341/ket9875.

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This review describes the lesions of the endocrine system that occur as a result of immunotherapy of cancer. This phenomenon is associated with the inhibition by monoclonal antibodies of checkpoints, which do not allow the immune system to affect tumor cells: CTLA-4, PD-1 and PD-L1. Immunotherapy by this group of drugs allows to increase the life expectancy of patients with cancer, but it also leads to the development of autoimmune endocrinopathies (thyroiditis, adrenalitis, diabetes mellitus, hypophysitis), which often manifest by life-threatening conditions. In view of the above, the necessi
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Brandão Neto, Rodrigo Antonio, and Jozélio Freire de Carvalho. "Diagnosis and classification of Addison's disease (autoimmune adrenalitis)." Autoimmunity Reviews 13, no. 4-5 (2014): 408–11. http://dx.doi.org/10.1016/j.autrev.2014.01.025.

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Reinehr, Thomas, Juliane Rothermel, Andreas Wegener-Panzer, Michaela F. Hartmann, Stefan A. Wudy, and Paul-Martin Holterhus. "Vanishing 17-Hydroxyprogesterone Concentrations in 21-Hydroxylase Deficiency." Hormone Research in Paediatrics 90, no. 2 (2018): 138–44. http://dx.doi.org/10.1159/000487927.

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We present a boy with a genetically proven congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. While massively elevated 17-hydroxyprogesterone (17-OHP) concentrations after birth led to the diagnosis, 17-OHP concentrations became immeasurable starting with the second year of life even though the dose of hydrocortisone was continuously decreased to ∼7 mg/m2/day. Furthermore, 17-OHP levels were immeasurable during the ACTH test and after withdrawing hydrocortisone medication. In contrast, ACTH levels increased after cessation of hydrocortisone treatment suggesting complete pri
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Green, S. T., J. P. Ng, and D. Chan-Lam. "Insulin-Dependent Diabetes Mellitus, Myasthenia Gravis, Pernicious Anaemia, Autoimmune Thyroiditis and Autoimmune Adrenalitis in a Single Patient." Scottish Medical Journal 33, no. 1 (1988): 213–14. http://dx.doi.org/10.1177/003693308803300112.

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Two classical autoimmune polyendocrine deficiency syndromes with heritable tendencies are described, Type 1 diabetes mellitus being associated with the Type 2 polyendocrine deficiency syndrome (Schmidt's syndrome). A man with Type 1 diabetes mellitus is described who developed an unusual combination of five autoimmune conditions (myasthenia gravis, Addisonian pernicious anaemia, adrenalitis and thyroiditis) which did not fit into the Type 1 or Type 2 classical polyendocrine deficiency syndromes. This suggests that the autoantibody, biochemical and haematological screening of affected individua
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Fujii, Yasuaki, Nobuo Kato, Junzo Kito, Junpei Asai, and Takashi Yokochi. "Experimental Autoimmune Adrenalitis: A Murine Model for Addison's Disease." Autoimmunity 12, no. 1 (1992): 47–52. http://dx.doi.org/10.3109/08916939209146129.

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Harris, P. E., and P. Kendall-Taylor. "Isolated aldosterone deficiency in a patient with autoimmune adrenalitis." American Journal of Medicine 90, no. 1 (1991): 124. http://dx.doi.org/10.1016/0002-9343(91)90515-y.

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Book chapters on the topic "Autoimmune Adrenalitis"

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Neto, Rodrigo Antonio Brandão, and Jozélio Freire de Carvalho. "Autoimmune Adrenalitis." In Autoimmune Disease Diagnosis. Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-69895-8_52.

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de Carvalho, Jozélio Freire, and Rodrigo Antonio Brandão Neto. "Autoimmune Addison Disease or Autoimmune Adrenalitis." In Diagnostic Criteria in Autoimmune Diseases. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-285-8_47.

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BETTERLE, CORRADO, and RENATO ZANCHETTA. "Adrenalitis." In The Autoimmune Diseases. Elsevier, 2006. http://dx.doi.org/10.1016/b978-012595961-2/50040-8.

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Betterle, Corrado, Fabio Presotto, and Renato Zanchetta. "Adrenalitis." In The Autoimmune Diseases. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-812102-3.00042-7.

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Betterle, Corrado, and Renato Zanchetta. "Adrenalitis." In The Autoimmune Diseases. Elsevier, 2014. http://dx.doi.org/10.1016/b978-0-12-384929-8.00042-3.

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Nosé, Vania. "Autoimmune Adrenalitis." In Diagnostic Pathology: Endocrine. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-52480-3.50080-9.

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Betterle, Corrado, Chiara Sabbadin, and Fabio Presotto. "Adrenalitis." In The Rose and Mackay Textbook of Autoimmune Diseases. Elsevier, 2024. http://dx.doi.org/10.1016/b978-0-443-23947-2.00056-4.

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Butler, Gary, and Jeremy Kirk. "Adrenal gland disorders." In Paediatric Endocrinology and Diabetes. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198786337.003.0008.

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• The fetal adrenal gland has an additional cortex which atrophies after birth. • Postnatally, there are three zones to the cortex: ◦ glomerulosa producing mineralocorticoids ◦ fasciculata producing cortisol ◦ reticularis producing androgens. • Adrenarche is a maturation process from age 6 years with an increase in androgens. • Acute adrenal crisis presents with: ◦ low sodium ◦ high potassium ◦ cortisol low/undetectable. • ACTH raised in primary causes, low in secondary. • Primary insufficiency may be congenital dysplasia (adrenal hypoplasia congenita) and enzyme blocks: congenital adrenal hyp
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