Hypophysitis Research Center

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  1. M. F. A. Rafiq, U. Farooq, A. A. Khan and N. U. Ain, Lymphocytic hypophysitis. A rare autoimmune disorder that presents as large suprasellar mass with complete resolution with steroids. J Ayub Med Coll Abbottab, 2015. 481-484. View PDF
  2. X. Kong, R. Wang, Y. Yang, H. Wu, C. Su, W. Ma, Y. Li, B. Xing, W. Lian, Z. Xu, Y. Yao and Z. Ren, Idiopathic Granulomatous Hypophysitis Mimicking Pituitary Abscess. Medicine (Baltimore), 2015. e1099. View PDF
  3. M. Cavusoglu, E. Elverici, S. Duran, E. Komut, S. Gurecci and B. Sakman, Idiopathic granulomatous hypophysitis: a rare cystic lesion of the pituitary. Intern Med, 2015. 1407-1410. View PDF
  4. R. Sellayah, M. Gonzales, S. Fourlanos and J. King, Lymphocytic hypophysitis in the elderly. J Clin Neurosci, 2015. . View PDF
  5. Y. Nakasone, K. Oguchi, Y. Sato, Y. Okubo, K. Yamauchi and T. Aizawa, Rapid conversion of autoimmune hypophysitis to an empty sella with immediate lowering of the serum IgG4 level. Neuro Endocrinol Lett, 2015. 112-114. View PDF
  6. M. E. Blanco-Canto, P. Davila-Gonzalez, C. Lopez de Silanes, M. L. Cuadrado-Perez, G. Ortega and J. Porta-Etessam, [Lymphocytic hypophysitis and hypertrophic pachymeningitis: description of a possible case associated to IgG4 pathologies]. Rev Neurol, 2015. 504-508. View PDF
  7. J. M. Lee, S. M. Park, B. H. Hwang, H. S. Choi, S. S. Lee, J. Y. Kim, S. R. Kim, K. W. Lee, H. Y. Son, K. S. K. and S. J. Yoo, A case of lymphocytic infunbibulo-neurophypophysitis with central diabetes insispidus improved after conservative care. J Korean Endocr Soc, 2008. 142-147. View PDF
  8. H. B. Chae, J. Y. Park, Y. K. Shong, K. J. Kim, C. H. Kim, B. D. Kwun, G. Y. Choe, J. B. Hwang and G. S. Kim, A case of lymphocytic infundibulo-neurohypophysitis. Korean J Med, 1997. 424-428. View PDF
  9. S. R. Oh, J. M. Cha, A. R. Jin, J. B. Park, H. Y. Kim, B. H. Park and C. G. Cho, Lymphocytic infundibulo-neurohypophysitis presenting with central diabetes insipidus: a case report and review of previous Korean cases. Korean J Med, 2009. S122-S127. View PDF
  10. G. Y. Cho, J. R. Hahm, J. H. Kim, T. W. Kang, I. K. Chung, T. Y. Yang, J. H. Chung, Y. K. Min, Le, M. S., M. K. Lee, Y. L. Se and K. W. Kim, A case of lymphocytic infundibulo-neurohypophysitis presenting as central diabetes insipidus a nodular mass on neurohypophysis. Korean J Med, 2001. 168-172. View PDF
  11. Y. H. Lee, Y. B. Kim, J. H. Lee, K. H. Jeong, M. K. Kim, K. S. Song and Y. S. Jo, A case of giant cell granulomatous hypophysitis with recurrent hypo-osmolar hyponatremia. Endocrinol Metab, 2010. 347-353. View PDF
  12. H. J. Oh, J. Y. Mok, J. E. Kim, S. B. Cho, S. A. Chang, J. H. Kim and J. M. Lee, Primary granulomatous hypophysitsi presenting with panhypopituitarism and central diabetes insipidus. Korean J Med, 2015. 581-586. View PDF
  13. J. Idiculla, S. Pakalomattom, A. P. Desai, B. Philip and V. Shobha, Neurofibromatosis type 1 and lymphocytic hypophysitis: Single trigger and double shots?. Internet Journal of Rheumatology and Clinical Immunology, 2015. 1/3/2015. View PDF
  14. Z. Chen, T. Yuan and Y. Yan, Granulomatous hypophysitis with MRI: a case report. Chinese Journal of Radiology (China), 2015. 232. View PDF
  15. C. Tiu, I. D. Pezaro C Fau - Davis, M. Davis Id Fau - Grossmann, P. Grossmann M Fau - Parente and P. Parente, Early recognition of ipilimumab-related autoimmune hypophysitis in patients with metastatic melanoma: Case studies and recommendations for management. LID - 10.1111/ajco.12348 [doi]. Asia Pac J Clin Oncol, 2015. . View PDF
  16. H. Bando, H. Iguchi G Fau - Fukuoka, M. Fukuoka H Fau - Taniguchi, S. Taniguchi M Fau - Kawano, M. Kawano S Fau - Saitoh, K. Saitoh M Fau - Yoshida, R. Yoshida K Fau - Matsumoto, K. Matsumoto R Fau - Suda, H. Suda K Fau - Nishizawa, M. Nishizawa H Fau - T, A diagnostic pitfall in IgG4-related hypophysitis: infiltration of IgG4-positive cells in the pituitary of granulomatosis with polyangiitis. Pituitary, 2015. . View PDF
  17. A. J. Sommerfield, A. J. Lockman Ka Fau - Bathgate, A. W. Bathgate Aj Fau - Patrick and A. W. Patrick, Multifocal fibrosclerosis: a new case report. Annals of clinical biochemistry, 2008. 99-101. View PDF
  18. W. Fukuda, T. Kimura M Fau - Akaogi, M. Akaogi T Fau - Sako, K. Sako M Fau - Ohiwa, Y. Ohiwa K Fau - Yamamoto, G. Yamamoto Y Fau - Kato, H. Kato G Fau - Hayashi, T. Hayashi H Fau - Yoshikawa and T. Yoshikawa, Multifocal fibrosclerosis: retroperitoneal fibrosis associated with a suprasellar tumor and pachymeningitis. Intern Med, 2003. 1006-1010. View PDF
  19. B. Hanna, Y. M. Li, T. Beutler, P. Goyal and W. A. Hall, Xanthomatous hypophysitis. J Clin Neurosci, 2015. . View PDF
  20. Y. Harano, K. Honda, Y. Akiyama, L. Kotajima and H. Arioka, A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes Insipidus. , 2015. . View PDF
  21. B. L. Goldstein, D. J. Gedmintas L Fau - Todd and D. J. Todd, Drug-associated polymyalgia rheumatica/giant cell arteritis occurring in two patients after treatment with ipilimumab, an antagonist of ctla-4. Arthritis & Rheumatol, 2014. 768-769. View PDF
  22. R. L. Batista, l. S. Ramos, V. A. Cescato, N. R. C. Musolino, C. G. Borba, G. O. Silva, L. H. Moreno and M. B. C. C. Neto, Thickened pituitary stalk associated with a mass in the sphenoidal sinus: an alarm to suspect hypophysitis by IgG4?. Int Arch Otorhinolaryngol, 2014. . View PDF
  23. B. Pulluri, M. Palaniswamy and H. D. Nguyen, Visual vignette. Endocr Pract, 2014. 760. View PDF
  24. S. D. Ferguson, L. A. Waguespack Sg Fau - Langford, J. L. Langford La Fau - Ater, I. E. Ater Jl Fau - McCutcheon and I. E. McCutcheon, Fatal juvenile xanthogranuloma presenting as a sellar lesion: case report and literature review. , 2014. . View PDF
  25. F. Tang, H. M. Liu, S. Zhou, J. K. Liu, E. Xiao and C. Tan, MRI manifestations of xanthomatous hypophysitis: A case report and review of the literature. J Cent South Univ, 2015. 228-232. View PDF
  26. J. S. Gopal-Kothandapani, V. Bagga, S. B. Wharton, D. J. Connolly, S. Sinha and P. J. Dimitri, Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion. Endocrinology, diabetes & metabolism case reports, 2015. . View PDF
  27. C. Pocha, J. Roat and K. Viskocil, Immune-mediated colitis: important to recognize and treat. J Crohns Colitis, 2014. 181-182. View PDF
  28. D. R. Minor, B. S. R. and J. Doyle, Lymphocytic vasculitis of the uterus in a patient with melanoma receiving ipilimumab. J Clin Oncol, 2013. e356. View PDF
  29. A. Jain and D. K. Dhanwal, A rare case of autoimmune hypophysitis presenting as temperature dysregulation. Journal of Clinical and Diagnostic Research, 2015. 9/10/2015. View PDF
  30. D. Majchel and M. T. Korytkowski, Anticytotoxic T-lymphocyte antigen-4 induced autoimmune hypophysitis: a case report and literature review. Case reports in endocrinology, 2015. 570293. View PDF
  31. C. Hida, T. Yamamoto, K. Endo, Y. Tanno, T. Saito and T. Tsukamoto, Inflammatory involvement of the hypophysis in Tolosa-Hunt syndrome. Intern Med, 1995. 1093-1096. View PDF
  32. T. J. Cummings, C. T. Chu and C. M. Hulette, December 1998--16 year old female with headaches, lethargy and a sellar/suprasellar mass. Brain pathology (Zurich, Switzerland), 1999. 425-426. View PDF
  33. N. Komoribayashi, H. Arai, Y. Kubo, T. Beppu, K. Ogasawara, T. Sugai, S. Nakamura and A. Ogawa, [Granulomatous change of the pituitary stalk caused by Rathke's cleft cyst: a case report]. No Shinkei Geka, 2003. 1193-1196. View PDF
  34. T. Nishikawa, J. A. Takahashi, A. Shimatsu and N. Hashimoto, Hypophysitis caused by Rathke's cleft cyst. Case report. Neurol Med Chir (Tokyo), 2007. 136-139. View PDF
  35. W. Thiryayi, M. H. Donaldson, D. Border and A. Tyagi, An enhancing pituitary lesion in a young woman: a diagnostic dilemma. J Clin Neurosci, 2007. 286-288. View PDF
  36. B. W. Scheithauer, A. I. Silva, J. L. Atkinson, T. B. Nippoldt, T. J. Kaufmann, K. Kovacs, E. Horvath and R. Lloyd, Pituitary adenoma with tumoral granulomatous reaction. Endocr Pathol, 2007. 86-90. View PDF
  37. M. Koutourousiou and A. Seretis, Aseptic meningitis after transsphenoidal management of Rathke's cleft cyst: case report and review of the literature. Neurol Sci, 2011. 323-326. View PDF
  38. Y. Miyajima, H. Oka, S. Utsuki and K. Fujii, Rathke's cleft cyst with xanthogranulomatous change--case report. Neurol Med Chir (Tokyo), 2011. 740-742. View PDF
  39. A. Muroi, S. Takano, T. Fukushima, T. Shimizu and A. Matsumura, Intracranial germinoma manifesting as cavernous sinus syndrome--case report. Neurol Med Chir (Tokyo), 2012. 754-756. View PDF
  40. L. Giammattei, H. Maslehaty, A. K. Petridis and H. M. Mehdorn, Lymphocitic infundibulo-neurohypophysitis mimicking a pituitary adenoma. Clinics and practice, 2011. e48. View PDF
  41. M. Nwokolo and J. Fletcher, A rare case of hypopituitarism with psychosis. Endocrinology, diabetes & metabolism case reports, 2013. 130007. View PDF
  42. K. Yamashita, T. Doden, M. Tanaka, Y. Funase, K. Yamauchi, T. Furukawa, K. Oguchi, T. Koyama and T. Aizawa, Paradoxical surge of corticotropin after glucocorticoid replacement in central adrenal insufficiency. Neuro Endocrinol Lett, 2012. 113-117. View PDF
  43. C. Jost, R. Krause, W. Graninger and K. Weber, Transient hypopituitarism in a patient with nephropathia epidemica. BMJ case reports, 2009. . View PDF
  44. P. Sanchez Sobrino, C. Paramo Fernandez, J. L. Lamas Ferreiro, B. Mantinan Gil, R. Palmeiro Carballeira and R. V. Garcia-Mayor, [Behcet disease with isolated ACTH deficiency]. Endocrinol Nutr, 2009. 463-466. View PDF
  45. M. W. Strachan, J. D. Walker and A. W. Patrick, Severe hypercalcaemia secondary to isolated adrenocorticotrophic hormone deficiency and subacute thyroiditis. Annals of clinical biochemistry, 2003. 295-297. View PDF
  46. P. J. Watkins, C. Gayle, N. Alsanjari, F. Scaravilli, M. Zanone and P. K. Thomas, Severe sensory-autonomic neuropathy and endocrinopathy in insulin-dependent diabetes. QJM : monthly journal of the Association of Physicians, 1995. 795-804. View PDF
  47. S. Okuno, M. Inaba, Y. Nishizawa and H. Morii, [Isolated ACTH deficiency associated with Hashimoto disease]. Nihon Rinsho, 1993. 2721-2725. View PDF
  48. R. C. Martin-Du Pan, D. Rouiller and M. Goumaz, [Isolated ACTH deficiency and primary thyroid insufficiency in an atopic patient: hypophysitis?]. Schweiz Med Wochenschr, 1994. 806-809. View PDF
  49. J. M. Garcin, C. Pharaboz, J. P. Laborde, B. Ceccaldi, R. Clement and B. Bauduceau, [Premenopausal hyperprolactinemia revealing pseudotumoral hypophysitis]. Presse Med, 1995. 1134. View PDF
  50. Z. Hochberg, D. Hardoff, D. Atias and A. Spindel, Isolated ACTH deficiency with transitory GH deficiency. J Endocrinol Invest, 1985. 67-70. View PDF
  51. D. Dewailly, M. F. Bourdelle-Hego, A. Pouplard-Barthelaix and P. Fossati, Recovery of ovulatory menstrual cycles under hydrocortisone in two amenorrheic women with isolated corticotropin deficiency. Horm Res, 1988. 14-16. View PDF
  52. G. Bellastella, A. Bizzarro, E. Aitella, M. Barrasso, D. Cozzolino, S. Di Martino, K. Esposito and A. De Bellis, PREGNANCY MAY FAVOUR THE DEVELOPMENT OF SEVERE AUTOIMMUNE CENTRAL DIABETES INSIPIDUS IN WOMEN WITH VASOPRESSIN-CELL ANTIBODIES: DESCRIPTION OF TWO CASES. Eur J Endocrinol, 2014. . View PDF
  53. H. Gulwani, M. Tripathi and N. Garg, Lymphocytic hypophysitis in non-pregnant middle-aged females mimicking pituitary adenoma: a report of two cases. Journal of postgraduate medicine, 2014. 421-422. View PDF
  54. Li, Z., W. Guan, Z. YUang, and Z. Li, Unusual IgG4-related hypophysitis: one case report and analysis of clinicopathological characteristics. Chin J Contemp Neurol Neurosurg, 2014. 889-896. View PDF
  55. Mitra, S., B. Choudhury, and H. Chakraborty, Primary granulomatous hypophysitis: An interesting entity. Indian J Pathol Microbiol, 2014. 650-2. View PDF
  56. Pena, J.A., S. Birchansky, and T.E. Lotze, Lymphocytic hypophysitis associated with pediatric multiple sclerosis. Pediatr Neurol, 2014. 580-2. View PDF
  57. Yildirim, A.E., D. Divanlioglu, N.E. Cetinalp, S. Sahin, S. Kulacoglu, and A.D. Belen, Primary non-necrotizing granulomatous hypophysitis mimicking pituitary adenomas. Turk Neurosurg, 2014. 688-94. View PDF
  58. Xu, C., A. Ricciuti, P. Caturegli, C.D. Keene, and A.Y. Kargi, Autoimmune lymphocytic hypophysitis in association with autoimmune eye disease and sequential treatment with infliximab and rituximab. Pituitary, 2014. . View PDF
  59. Kim, H.J., Triphasic Pattern of Diabetes Insipidus in a Pregnant Woman With a Rathke's Cleft Cyst and Hypophysitis. Am J Med Sci, 2014. . View PDF
  60. Dow, A., R.V. Russell, V. Bonert, J. Carmichael, A. Mamelak, B.D. Pressman, X. Fan, and R. Yu, A Protracted and Aggressive Variant of Lymphocytic Hypophysitis with Mammillary Body Involvement and Cognitive Dysfunction. Endocr Pract, 2014. 1/15/2014. View PDF
  61. Tanaka, J., A. Arai, S. Hayashi, Y. Sakagami, K. Araki, S. Kakiuchi, T. Nomura, K. Kuwamura, and E. Kohmura, A case of possible immunoglobulin G4-related disease (IgG4-RD) with retroperitoneal fibrosis and central diabetes insipidus due to infundibulohypophysitis. No Shinkei Geka, 2014. 561-6. View PDF
  62. Manousaki, D., C. Deal, J.J. De Bruycker, P. Ovetchkine, C. Mercier, and N. Alos, A 15-year-old adolescent with a rare pituitary lesion. Endocrinol Diabetes Metab Case Rep, 2014. 140010. View PDF
  63. Nallapaneni, N.N., R. Mourya, V.R. Bhatt, S. Malhotra, A.K. Ganti, and K.K. Tendulkar, Ipilimumab-induced hypophysitis and uveitis in a patient with metastatic melanoma and a history of ipilimumab-induced skin rash. J Natl Compr Canc Netw, 2014. 1077-81. View PDF
  64. Arango Fragoso, E., M. Alvaro Navidad, J. Cordero Ruiz, and F.J. Plaza Arraz, Hipofisitis linfocitaria en gestante de 34 semana. Progresos de Obstetricia y Ginecologia, 2013. . View PDF
  65. Chodakiewitz, Y., S. Brown, J.L. Boxerman, J.M. Brody, and J.M. Rogg, Ipilimumab treatment associated pituitary hypophysitis: Clinical presentation and imaging diagnosis. Clin Neurol Neurosurg, 2014. 125-130. View PDF
  66. Ohkubo, Y., T. Sekido, K. Takeshige, H. Ishi, M. Takei, S. Nishio, M. Yamazaki, M. Komatsu, S. Kawa, and S. Suzuki, Occurrence of IgG4-related hypophysitis lacking IgG4-bearing plasma cell infiltration during steroid therapy. Intern Med, 2014. 753-7. View PDF
  67. Matoba, K., S. Mitsuishi, S. Hayashida, and H. Yamazaki, Hypopituitarism possibly due to lymphocytic hypophysitis in a patient with type 1 diabetes. Intern Med, 2014. 1961-4. View PDF
  68. Sakai, T., M. Kondo, S. Yoshii, and H. Tomimoto, IgG4-related disease that presented cranial, cervical, lumbar and sacral hypertrophic pachymeningitis associated with infundibulo-hypophysitis. Rinsho Shinkeigaku, 2014. 664-7. View PDF
  69. Khong, P., A. Enno, and B. Darwish, Lymphoplasmacytic hypophysitis associated with immunoglobulin G4. J Clin Neurosci, 2014. 342-4. View PDF
  70. Nishina, N., Y. Kaneko, M. Kuwana, H. Hanaoka, H. Kameda, S. Mikami, and T. Takeuchi, IgG4-Related Disease without Overexpression of IgG4: Pathogenesis Implications. Case Rep Rheumatol, 2012. 754935. View PDF
  71. Sutton, R.A., M. Voskoboynik, G.A. McArthur, and J. Lokan, Autoimmune hypophysitis in a patient successfully treated with anti-CTLA-4 (ipilimumab) immunotherapy for metastatic malignant melanoma. Pathology, 2013. S84. View PDF
  72. Talib, S.H., M. Naik, A.R. Tapadia, and A.M. Inamdar, Lymphocytic hypophysitis: A rare presentation. JIACM, 2013. 166-168. View PDF
  73. Suzuki, H., K. Hayashi, and T. Fukunaga, Two forensic autopsy cases of death from unexpected lesions of the pituitary gland. Leg Med (Tokyo), 2013. . View PDF
  74. Kanoke, A., Y. Ogawa, M. Watanabe, T. Kumabe, and T. Tominaga, Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature. BMC Res Notes, 2013. 560. View PDF
  75. Kaneko, S., M. Shiozaki, N. Omori, S. Tsuruta, H. Haraoka, and Y. Tsukamoto, Latent pregnancy-associated hypopituitarism accompained by chronic thyroiditis and limited scleroderma, revealed by the breakout of adrenal insufficiency 42 years after delivery. Endocrinol Studies, 2013. 15-18. View PDF
  76. Iseda, I., K. Hida, A. Tone, M. Tenta, Y. Shibata, K. Matsuo, I. Yamadori, and K. Hashimoto, Prednisolone markedly reduced serum IgG4 levels along with the improvement of pituitary mass and anterior pituitary function in a patient with IgG4-related infundibulo-hypophysitis. Endocr J, 2013. . View PDF
  77. Guzzo, M.F., C.B. Bueno, T.T. Amancio, S. Rosemberg, C. Bueno, E.L. Arioli, A. Glezer, and M.D. Bronstein, An intrasellar germinoma with normal tumor marker concentrations mimicking primary lymphocytic hypophysitis. Arq Bras Endocrinol Metabol, 2013. 566-70. View PDF
  78. Dharmshaktu, P., M. Singh, and D. Dhanwal, Lymphocytic hypophysitis presenting as a visual threatening sellar mass and its complete recovery with oral steroids: think beyond surgery. Endocrinol Studies, 2013. 31-33. View PDF
  79. Bot, I., C.U. Blank, W. Boogerd, and D. Brandsma, Neurological immune-related adverse events of ipilimumab. Pract Neurol, 2013. 278-80. View PDF
  80. Baruah, M.P., C.J. Das, and N. Medhi, Cystic pituitary mass: an unusual presentation of autoimmune hypophysitis. A case report.. Int J Clin Cases Invest, 2010. 1/2/2014. View PDF
  81. Ahsan, T. and Z. Banu, Lymphocytic infundibulo-neurohypophysitis with secondary empty sella. J Endocrinol Metab, 2013. 57-61. View PDF
  82. Cocco C, Meloni A, Boi F, Pinna G, Possenti R, Mariotti S, Ferri GL, Median eminence dopaminergic nerve terminals: a novel target in autoimmune polyendocrine syndrome?. J Clin Endocrinol Metab, 2005. 4108-4111. View PDF
  83. Anderson L, Bhatia V, Ipilimumab immune-related adverse reactions: a case report. South Dakota medicine : the journal of the South Dakota State Medical Association, 2013. 315-317. View PDF
  84. Kacem FH, Charfi N, Mnif MF, Kamoun M, Akid F, Mnif F, Naceur BB, Rekik N, Mnif Z, Abid M, Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a woman. Indian journal of endocrinology and metabolism, 2013. S107-S110. View PDF
  85. Takahashi D, Kobayashi H, Kubota K, Suzuki Y, Nakamura A, Ishizu K, Nakanishi M, Nagashima T, Tajima T, A rare association between Rathke's cyst and hypophysitis in a patient with delayed sex development and growth failure. J Pediatr Endocrinol Metab, 2013. 949-953. View PDF
  86. Laing, I., L. McWilliam, D. Owen, M. Drayson, and D. Riley, Secondary adrenal failure in a young woman presenting as hypoglycaemic coma. Ann Clin Biochem, 1998. 545-8. View PDF
  87. Jevalikar G, Wong SC, Zacharin M, Rapidly evolving hypopituitarism in a boy with multiple autoimmune disorders. Journal of paediatrics and child health, 2013. 783-785. View PDF
  88. Iwama S, Welt CK, Romero CJ, Radovick S, Caturegli P, Isolated Prolactin Deficiency Associated With Serum Autoantibodies Against Prolactin-Secreting Cells. J Clin Endocrinol Metab, 2013. 3920-3925. View PDF
  89. Gao H, Gu YY, Qiu MC, Autoimmune hypophysitis may eventually become empty sella. Neuro Endocrinol Lett, 2013. 102-106. View PDF
  90. Dhanwal DK, Dharamshaktu P, Autoimmune hypophysitis. The Indian journal of medical research, 2013. 995-996. View PDF
  91. Husain Q, Zouzias A, Kanumuri VV, Eloy JA, Liu JK, Idiopathic granulomatous hypophysitis presenting as pituitary apoplexy. J Clin Neurosci, 2013. . View PDF
  92. de Hollanda A, Aranda GB, Mora M, Gaba L, Halperin I, Ipilimumab, a cause of autoimmune hypophysitis. Endocrinol Nutr, 2013. . View PDF
  93. Caputo C, Bazargan A, McKelvie PA, Sutherland T, Su CS, Inder WJ, Hypophysitis due to IgG4-related disease responding to treatment with azathioprine: an alternative to corticosteroid therapy. Pituitary, 2013. . View PDF
  94. Broekman M, Goedee SH, Nieuwlaat WA, Depauw P, Corticosteroid treatment buys time in case of a newly diagnosed hypophysitis with visual deterioration. BMJ case reports, 2013. . View PDF
  95. Bianchi A, Mormando M, Doglietto F, Tartaglione L, Piacentini S, Lauriola L, Maira G, De Marinis L, Hypothalamitis: a diagnostic and therapeutic challenge. Pituitary, 2013. . View PDF
  96. Shillo P, Evans R, Wright J, Newell Price J, Iatrogenic lymphocytic hypophysitis. Endocrine Abstracts, 2011. P617. View PDF
  97. Joung JY, Jeong H, Cho YY, Huh K, Suh YL, Kim KW, Bae JC, Steroid Responsive Xanthomatous Hypophysitis Associated with Autoimmune Thyroiditis: A Case Report. Endocrinol Metab, 2013. 65-69. View PDF
  98. Miyoshi T, Otsuka F, Tsukamoto N, Suzuki J, Otani H, Goto J, Ogura T, Tanaka Y, Hattori T, Makino H, A case of suspected hypothalamo-pituitary dysfunction due to IgG4-related disease. The Japanese journal of endocrinology, 2008. 87-89. View PDF
  99. Katabami T, Shirai M, Hayashi A, Naito S, Saito N, Kato M, Odanaka M, A case of autoimmune hypophysitis with Mikulicz's syndrome. The Japanese journal of endocrinology, 2003. 5/9/2013. View PDF
  100. Molitch ME, Hedley-Whyte ET, Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 5-1985. A 33-year-old woman with pituitary dysfunction and diabetes mellitus. N Engl J Med, 1985. 297-305. View PDF
  101. Chung CH, Song MS, Cho HD, Jeong du S, Kim YJ, Bae HG, Kim SJ, A case of idiopathic granulomatous hypophysitis. Korean J Intern Med, 2012. 346-349. View PDF
  102. Unlu E, Puyan FO, Bilgi S, Kemal Hamamcioglu M, Granulomatous hypophysitis: presentation and MRI appearance. J Clin Neurosci, 2006. 1062-1066. View PDF
  103. Gundgurthi A, Kharb S, Garg MK, Brar KS, Bharwaj R, Gupta S, Pathak HC, Combined granulomatous and lymphocytic hypophysitis presenting as pituitary incidentaloma in a middle-aged woman. Indian journal of endocrinology and metabolism, 2012. 846-849. View PDF
  104. Padilla-Martinez JJ, Gonzalez-Cornejo S, Alvarez-Palazuelos LE, Villagomez-Mendez JA, Chiquete E, Dominguez-Rosales JA, Espejo-Plascencia I, Gonzalez-Diaz E, Torres-Baranda JR, Ruiz-Sandoval JL, Granulomatous hypophysitis by Mycobacterium gordonae in a non HIV-infected patient. Neurology international, 2009. e18. View PDF
  105. Gupta V, Nagpal RD, Venkatram S, Patel A, Idiopathic granulomatous hypophysitis presenting as panhypopituitarism. The Endocrinologist, 2010. 102-104. View PDF
  106. Babey M, Aeberli D, Vajtai I, Sahli R, Acute onset of polyarthralgia and high anti-cyclic citrullinated peptide antibodies in a case of idiopathic granulomatous hypophysitis. J Rheumatol, 2009. 204-207. View PDF
  107. Murakami M, Nishioka H, Izawa H, Ikeda Y, Haraoka J, Granulomatous hypophysistis associated with rathke's cleft cyst: a case report. Minim Invasive Neurosurg, 2008. 169-172. View PDF
  108. Husain N, Husain M, Rao P, Pituitary tuberculosis mimicking idiopathic granulomatous hypophysitis. Pituitary, 2008. 313-315. View PDF
  109. Bhansali A, Kumar A, Dutta P, Bhadada S, Khandelwal N, Das Radotra B, A woman with pituitary mass presenting as oligomenorrhea and later acute renal failture. The Endocrinologist, 2008. 13-15. View PDF
  110. Oelbaum MH, Wainwright J, Hypopituitarism in a Male due to Giant Cell Granuloma of the Anterior Pituitary. J Clin Pathol, 1950. 122-129. View PDF
  111. Mehndiratta MM, Phul P, Singh AK, Garg S, Bali R, Granulomatous hypophysitis--an interesting and rare cause mimicking pituitary mass. J Assoc Physicians India, 2007. 653-654. View PDF
  112. Garcia Alzamora M, Muller K, Spreer J, Manifestation of idiopathic granulomatous hypophysitis as hormone-active pituitary adenoma. Rofo, 2007. 84-85. View PDF
  113. Dutta P, Hayatbhat M, Bhansali A, Bambery P, Kakar N, Wegener's granulomatosis presenting as diabetes insipidus. Exp Clin Endocrinol Diabetes, 2006. 533-536. View PDF
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