{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,28]],"date-time":"2026-04-28T22:17:13Z","timestamp":1777414633355,"version":"3.51.4"},"reference-count":22,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2016,10,5]],"date-time":"2016-10-05T00:00:00Z","timestamp":1475625600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["APMIS"],"published-print":{"date-parts":[[2016,12]]},"abstract":"<jats:p>Hypophysitis includes three histopathologically distinct entities \u2013 granulomatous, lymphocytic and xanthomatous forms. Etiopathogenesis and the immunological differences among these is not well characterized. This study aims to explore the immunopathogenesis of granulomatous and lymphocytic forms of hypophysitis. Demographic, clinical, endocrine function and radiological features of 33 histologically confirmed cases of hypophysitis were reviewed. Immunophenotyping of inflammatory component was performed in 13\/33 cases. Visual disturbances (46%), headache (36%), polyuria\/polydipsia (6%), menstrual disturbance (6%) and galactorrhoea (6%) were the frequent presenting symptoms. Endocrine abnormalities were noted in 11\/18 cases evaluated (61%). Hypothyroidism was the most common endocrine abnormality (33.33%) followed by hyperprolactinaemia (22%) and hypocortisolism (16.66%). On neuroimaging, sellar mass with variable contrast enhancement was observed. On histology, granulomatous hypophysitis (<jats:styled-content style=\"fixed-case\">GH<\/jats:styled-content>) was more common (84.84%) than lymphocytic hypophysitis (<jats:styled-content style=\"fixed-case\">LH<\/jats:styled-content>) (15.15%). In <jats:styled-content style=\"fixed-case\">GH<\/jats:styled-content>, the infiltrate had almost equal proportions of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>3+ T cells and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>68+ histiocytes. Cytotoxic T cells (<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8+) predominated [<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4:<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8 &lt; 1]. <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>20+ B cell component ranged from &lt;5% to 50%. Fibrosis, necrosis and giant cells accompanied <jats:styled-content style=\"fixed-case\">GH<\/jats:styled-content>. <jats:styled-content style=\"fixed-case\">LH<\/jats:styled-content> in contrast, had <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4+ T\u2010helper cell predominance [CD4: CD8 &gt; 1]. <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>68+ histiocytes constituted &lt;20% and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>20+ B cells, 5\u201340% of the infiltrates. In conclusion, <jats:styled-content style=\"fixed-case\">GH<\/jats:styled-content> revealed cytotoxic T cell and histiocyte rich infiltrate in contrast to <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4+ T\u2010cell predominance in <jats:styled-content style=\"fixed-case\">LH<\/jats:styled-content> suggesting that the two forms have distinct immunological mechanisms in evolution, an autoimmune process in <jats:styled-content style=\"fixed-case\">LH<\/jats:styled-content> and type <jats:styled-content style=\"fixed-case\">IV<\/jats:styled-content> hypersensitivity response in <jats:styled-content style=\"fixed-case\">GH<\/jats:styled-content>.<\/jats:p>","DOI":"10.1111\/apm.12603","type":"journal-article","created":{"date-parts":[[2016,10,12]],"date-time":"2016-10-12T17:57:38Z","timestamp":1476295058000},"page":"1072-1077","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":13,"title":["Granulomatous and lymphocytic hypophysitis \u2013 are they immunologically distinct?"],"prefix":"10.1111","volume":"124","author":[{"given":"Shilpa","family":"Rao","sequence":"first","affiliation":[{"name":"Department of Neuropathology National Institute of Mental Health and Neurosciences Bangalore India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anita","family":"Mahadevan","sequence":"additional","affiliation":[{"name":"Department of Neuropathology National Institute of Mental Health and Neurosciences Bangalore India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tanmoy","family":"Maiti","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery National Institute of Mental Health and Neurosciences Bangalore India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manish","family":"Ranjan","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery National Institute of Mental Health and Neurosciences Bangalore India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shivayogi Durgad","family":"Shwetha","sequence":"additional","affiliation":[{"name":"Human Brain Tissue Repository National Institute of Mental Health and Neurosciences Bangalore India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Arimappamagan","family":"Arivazhagan","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery National Institute of Mental Health and Neurosciences Bangalore India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jitender","family":"Saini","sequence":"additional","affiliation":[{"name":"Neuroimaging and Intervention Radiology National Institute of Mental Health and Neurosciences Bangalore 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