MECHANISMS IN ENDOCRINOLOGY: Hypophysitis: diagnosis and treatment.

作者: Mamta N Joshi , Benjamin C Whitelaw , Paul V Carroll

DOI: 10.1530/EJE-17-0009

关键词:

摘要: Hypophysitis is a rare condition characterised by inflammation of the pituitary gland, usually resulting in hypopituitarism and enlargement. Pituitary can occur as primary hypophysitis (most commonly lymphocytic, granulomatous or xanthomatous disease) secondary (as result systemic diseases, immunotherapy alternative sella-based pathologies). be classified using anatomical, histopathological aetiological criteria. Non-invasive diagnosis remains elusive, use currently available serum anti-pituitary antibodies are limited low sensitivity specificity. Newer markers such anti-rabphilin 3A yet to show consistent diagnostic value not commercially available. Traditionally considered very condition, recent recognition IgG4-related disease consequence immune modulatory therapy has resulted increased understanding pathophysiology hypophysitis. Modern imaging techniques, histological classification profiling improving accuracy patient with The objective this review bring readers up-to-date current conditions presenting hypophysitis, focussing on advances areas for future development. We describe features, investigation approach likely including existing conventional techniques those research/development arena. results acute persistent hormone deficiency requiring long-term replacement. Management includes control inflammatory mass variety treatment strategies surgery medical therapy. Glucocorticoids remain mainstay but other immunosuppressive agents (e.g. azathioprine, rituximab) benefit some cases, there need controlled studies inform practice.

参考文章(88)
You-you Gu, Hua Gao, Ming-cai Qiu, Autoimmune hypophysitis may eventually become empty sella Neuro endocrinology letters. ,vol. 34, pp. 102- 106 ,(2013)
Hironori Bando, Genzo Iguchi, Masaaki Yamamoto, Ryoko Hidaka-Takeno, Yutaka Takahashi, Anti-PIT-1 antibody syndrome; a novel clinical entity leading to hypopituitarism. Pediatric endocrinology reviews. ,vol. 12, pp. 290- 296 ,(2015)
Sara Bacanovic, Irene A. Burger, Paul Stolzmann, Jürg Hafner, Martin W. Huellner, Ipilimumab-induced adrenalitis: a possible pitfall in 18F-FDG-PET/CT Clinical Nuclear Medicine. ,vol. 40, ,(2015) , 10.1097/RLU.0000000000000887
Jun-ichi IKEDA, Jun-ichi KURATSU, Masaki MIURA, Yutaka KAI, Yukitaka USHIO, Lymphocytic adenohypophysitis accompanying occlusion of bilateral internal carotid arteries--case report. Neurologia Medico-chirurgica. ,vol. 30, pp. 346- 349 ,(1990) , 10.2176/NMC.30.346
Bette K. Kleinschmidt-DeMasters, M. Beatriz S. Lopes, Update on hypophysitis and TTF-1 expressing sellar region masses. Brain Pathology. ,vol. 23, pp. 495- 514 ,(2013) , 10.1111/BPA.12068
Zachary S. Wallace, Vikram Deshpande, Hamid Mattoo, Vinay S. Mahajan, Maria Kulikova, Shiv Pillai, John H. Stone, IgG4-Related Disease: Clinical and Laboratory Features in One Hundred Twenty-Five Patients. Arthritis & Rheumatism. ,vol. 67, pp. 2466- 2475 ,(2015) , 10.1002/ART.39205
Bernies van der Hiel, Christian U. Blank, John B.A.G. Haanen, Marcel P.M. Stokkel, Detection of Early Onset of Hypophysitis by 18F-FDG PET-CT in a Patient With Advanced Stage Melanoma Treated With Ipilimumab Clinical Nuclear Medicine. ,vol. 38, ,(2013) , 10.1097/RLU.0B013E3182639765
M. A. Landek-Salgado, P. Leporati, I. Lupi, A. Geis, P. Caturegli, Growth hormone and proopiomelanocortin are targeted by autoantibodies in a patient with biopsy-proven IgG4-related hypophysitis Pituitary. ,vol. 15, pp. 412- 419 ,(2012) , 10.1007/S11102-011-0338-8
Akira SHIMATSU, Yutaka OKI, Ichiro FUJISAWA, Toshiaki SANO, Pituitary and stalk lesions (infundibulo-hypophysitis) associated with immunoglobulin G4-related systemic disease: an emerging clinical entity. Endocrine Journal. ,vol. 56, pp. 1033- 1041 ,(2009) , 10.1507/ENDOCRJ.K09E-277