{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,4,15]],"date-time":"2023-04-15T14:41:42Z","timestamp":1681569702948},"reference-count":19,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["PED"],"published-print":{"date-parts":[[2013,3]]},"abstract":"<jats:p>The distinction between autoimmune hypophysitis and other non\u2013hormone secreting pituitary masses is often difficult to determine with certainty without pituitary biopsy and pathological examination. To aid in this distinction, the authors recently published a clinicoradiological scoring system, which they used in the case of a 15-year-old girl presented here. The patient presented with headache, visual field defects, polydipsia, and polyuria, and she was found to have secondary hypogonadism and hypoadrenalism. Magnetic resonance imaging showed a pituitary mass of approximately 2 cm in diameter. Application of the clinicoradiological parameters gave a score of \u22126, which favored a diagnosis of hypophysitis over that of adenoma. The presence of pituitary autoantibodies substantiated the diagnosis of hypophysitis. The patient was treated conservatively with high-dose prednisolone, and her symptoms improved markedly. This case illustrates the utility of using a clinicoradiological score when autoimmune hypophysitis is suspected since it can identify patients who can be treated without the need for pituitary surgery.<\/jats:p>","DOI":"10.3171\/2012.11.peds12432","type":"journal-article","created":{"date-parts":[[2013,1,4]],"date-time":"2013-01-04T15:01:07Z","timestamp":1357311667000},"page":"335-339","source":"Crossref","is-referenced-by-count":0,"title":["Use of a clinicoradiological score to determine the presurgical diagnosis of autoimmune hypophysitis in a teenage girl"],"prefix":"10.3171","volume":"11","author":[{"given":"Vivek","family":"Bose","sequence":"first","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Patrizio","family":"Caturegli","sequence":"additional","affiliation":[{"name":"Department of Pathology and Immunology and"},{"name":"Feinstone Department of Molecular Microbiology and Immunology, The Johns Hopkins University, Baltimore, Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jens","family":"Conrad","sequence":"additional","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wael","family":"Omran","sequence":"additional","affiliation":[{"name":"Endocrinology Practice, Mainz, Germany; and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Stephan","family":"Boor","sequence":"additional","affiliation":[{"name":"Neuroradiology, Gutenberg Medical University Mainz;"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alf","family":"Giese","sequence":"additional","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Angelika","family":"Gutenberg","sequence":"additional","affiliation":[{"name":"Departments of Neurosurgery and"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"key":"b1-peds12432","series-title":"Intern Med","doi-asserted-by":"publisher","first-page":"1565","DOI":"10.2169\/internalmedicine.49.3458","article-title":"Lymphocytic hypophysitis with a long latent period from onset of central diabetes insipidus to development of pituitary enlargement","volume":"49","author":"Akahori","year":"2010"},{"key":"b2-peds12432","series-title":"Ann Med Interne (Paris)","first-page":"327","article-title":"Lymphocytic hypophysitis. 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