Granulomatous and lymphocytic hypophysitis – are they immunologically distinct?. Issue 12 (5th October 2016)
- Record Type:
- Journal Article
- Title:
- Granulomatous and lymphocytic hypophysitis – are they immunologically distinct?. Issue 12 (5th October 2016)
- Main Title:
- Granulomatous and lymphocytic hypophysitis – are they immunologically distinct?
- Authors:
- Rao, Shilpa
Mahadevan, Anita
Maiti, Tanmoy
Ranjan, Manish
Shwetha, Shivayogi Durgad
Arivazhagan, Arimappamagan
Saini, Jitender - Abstract:
- Abstract : Hypophysitis includes three histopathologically distinct entities – 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 (GH) was more common (84.84%) than lymphocytic hypophysitis (LH) (15.15%). In GH, the infiltrate had almost equal proportions of CD3+ T cells and CD68+ histiocytes. Cytotoxic T cells (CD8+) predominated [CD4:CD8 < 1]. CD20+ B cell component ranged from <5% to 50%. Fibrosis, necrosis and giant cells accompanied GH. LH in contrast, had CD4+ T‐helper cell predominance [CD4: CD8 > 1]. CD68+ histiocytes constituted <20% and CD20+ B cells, 5–40% of the infiltrates. In conclusion, GHAbstract : Hypophysitis includes three histopathologically distinct entities – 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 (GH) was more common (84.84%) than lymphocytic hypophysitis (LH) (15.15%). In GH, the infiltrate had almost equal proportions of CD3+ T cells and CD68+ histiocytes. Cytotoxic T cells (CD8+) predominated [CD4:CD8 < 1]. CD20+ B cell component ranged from <5% to 50%. Fibrosis, necrosis and giant cells accompanied GH. LH in contrast, had CD4+ T‐helper cell predominance [CD4: CD8 > 1]. CD68+ histiocytes constituted <20% and CD20+ B cells, 5–40% of the infiltrates. In conclusion, GH revealed cytotoxic T cell and histiocyte rich infiltrate in contrast to CD4+ T‐cell predominance in LH suggesting that the two forms have distinct immunological mechanisms in evolution, an autoimmune process in LH and type IV hypersensitivity response in GH. … (more)
- Is Part Of:
- Apmis. Volume 124:Issue 12(2016:Dec.)
- Journal:
- Apmis
- Issue:
- Volume 124:Issue 12(2016:Dec.)
- Issue Display:
- Volume 124, Issue 12 (2016)
- Year:
- 2016
- Volume:
- 124
- Issue:
- 12
- Issue Sort Value:
- 2016-0124-0012-0000
- Page Start:
- 1072
- Page End:
- 1077
- Publication Date:
- 2016-10-05
- Subjects:
- Granulomatous hypophysitis -- lymphocytic hypophysitis -- immunopathogenesis -- cytotoxic T cells -- helper T cells
Pathology -- Periodicals
Microbiology -- Periodicals
Immunology -- Periodicals
572 - Journal URLs:
- http://www.blackwell-synergy.com/loi/apm ↗
https://onlinelibrary.wiley.com/journal/16000463 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apm.12603 ↗
- Languages:
- English
- ISSNs:
- 0903-4641
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1568.740000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2678.xml