Skip to main content
Top
Published in: Pituitary 5/2015

01-10-2015

Hypophysitis: a single-center case series

Authors: Brandon S. Imber, Han S. Lee, Sandeep Kunwar, Lewis S. Blevins, Manish K. Aghi

Published in: Pituitary | Issue 5/2015

Login to get access

Abstract

Purpose

The authors review their treatment experience and summarize clinical outcomes for patients with hypophysitis over the past 15 years.

Methods

A retrospective analysis was conducted on patients with lymphocytic, granulomatous or IgG4-related hypophysitis treated from 1997 to 2014 at a single academic center. Patients’ medical records were reviewed and binary logistic regression analysis was used to assess whether various clinical parameters were associated with improved outcomes including endocrine function, radiographic appearance and disease recurrence.

Results

Twenty-one patients (13 women and 8 men) were identified with a median diagnosis age of 37.4 years. All but two patients (90 %) were diagnosed histopathologically and the remaining two were diagnosed clinically with lymphocytic hypophysitis. 16 patients (76 %) had lymphocytic hypophysitis, 3 (14 %) had granulomatous hypophysitis, 1 (5 %) had IgG4-related hypophysitis and 1 (5 %) had mixed lymphocytic-granulomatous. Patients presented with various symptoms of expanding sellar mass with most common signs including headache (57 %), polyuria/polydipsia (52 %), vision changes (52 %) and amenorrhea or decreased libido (48 %). Pre-treatment endocrine evaluation revealed that 12 (57 %) patients had complete anterior hypopituitarism, 11 patients (52 %) had diabetes insipidus, ten patients (48 %) had mild hyperprolactinemia and three patients (14 %) had isolated endocrine axis deficiencies with partial gland function. We observed a broad diversity in pre-treatment imaging with common findings including uniform contrast enhancement (62 %), thickened infundibulum (57 %) and loss of hypophysis bright spot on T1 imaging (43 %). Patients were treated with steroids and hormone supplementation as needed. 16 patients (76 %) had recorded post-treatment MRI scans which revealed that half had radiographic improvement and half had stable or worsened post-treatment imaging. Only female gender was found to significantly predict improved odds of post-steroid radiographic improvement. For post-treatment endocrine evaluation, six patients (29 %) did not have an evaluation on record, four patients (19 %) had some improvement in at least one axis, seven patients (33 %) had stable but non-worsened endocrine function and four patients (19 %) had worsened endocrine function post-steroids.

Conclusions

Hypophysitis is an increasingly recognized diagnosis that can present with a broad array of radiographic and clinical features. Surgical biopsy can be helpful to make definitive diagnosis and may guide treatment decision-making.
Appendix
Available only for authorised users
Literature
1.
3.
go back to reference Leporati P, Landek-Salgado MA, Lupi I et al (2011) IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab 96:1971–1980PubMedCentralCrossRefPubMed Leporati P, Landek-Salgado MA, Lupi I et al (2011) IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab 96:1971–1980PubMedCentralCrossRefPubMed
4.
go back to reference Rivera J-A (2006) Lymphocytic hypophysitis: disease spectrum and approach to diagnosis and therapy. Pituitary 9:35–45CrossRefPubMed Rivera J-A (2006) Lymphocytic hypophysitis: disease spectrum and approach to diagnosis and therapy. Pituitary 9:35–45CrossRefPubMed
5.
go back to reference Khare S, Jagtap VS, Budyal SR et al (2013) Primary (autoimmune) hypophysitis: a single centre experience. Pituitary Khare S, Jagtap VS, Budyal SR et al (2013) Primary (autoimmune) hypophysitis: a single centre experience. Pituitary
6.
go back to reference Falorni A, Minarelli V, Bartoloni E et al (2014) Diagnosis and classification of autoimmune hypophysitis. Autoimmun Rev 13:412–416CrossRefPubMed Falorni A, Minarelli V, Bartoloni E et al (2014) Diagnosis and classification of autoimmune hypophysitis. Autoimmun Rev 13:412–416CrossRefPubMed
7.
go back to reference Goudie RB, Pinkerton PH (1962) Anterior hypophysitis and Hashimoto’s disease in a young woman. J Pathol Bacteriol 83:584–585CrossRefPubMed Goudie RB, Pinkerton PH (1962) Anterior hypophysitis and Hashimoto’s disease in a young woman. J Pathol Bacteriol 83:584–585CrossRefPubMed
9.
go back to reference Hamnvik O-PR, Laury AR, Laws ER, Kaiser UB (2010) Lymphocytic hypophysitis with diabetes insipidus in a young man. Nat Rev Endocrinol 6:464–470CrossRefPubMed Hamnvik O-PR, Laury AR, Laws ER, Kaiser UB (2010) Lymphocytic hypophysitis with diabetes insipidus in a young man. Nat Rev Endocrinol 6:464–470CrossRefPubMed
10.
go back to reference Bellastella A, Bizzarro A, Coronella C et al (2003) Lymphocytic hypophysitis: a rare or underestimated disease? Eur J Endocrinol Eur Fed Endocr Soc 149:363–376CrossRef Bellastella A, Bizzarro A, Coronella C et al (2003) Lymphocytic hypophysitis: a rare or underestimated disease? Eur J Endocrinol Eur Fed Endocr Soc 149:363–376CrossRef
11.
go back to reference De Bellis A, Sinisi AA, Conte M et al (2007) Antipituitary antibodies against gonadotropin-secreting cells in adult male patients with apparently idiopathic hypogonadotropic hypogonadism. J Clin Endocrinol Metab 92:604–607CrossRefPubMed De Bellis A, Sinisi AA, Conte M et al (2007) Antipituitary antibodies against gonadotropin-secreting cells in adult male patients with apparently idiopathic hypogonadotropic hypogonadism. J Clin Endocrinol Metab 92:604–607CrossRefPubMed
12.
go back to reference De Bellis A, Dello Iacovo A, Bellastella G et al (2014) Characterization of pituitary cells targeted by antipituitary antibodies in patients with isolated autoimmune diseases without pituitary insufficiency may help to foresee the kind of future hypopituitarism. Pituitary 17:457–463 De Bellis A, Dello Iacovo A, Bellastella G et al (2014) Characterization of pituitary cells targeted by antipituitary antibodies in patients with isolated autoimmune diseases without pituitary insufficiency may help to foresee the kind of future hypopituitarism. Pituitary 17:457–463
13.
go back to reference Torino F, Barnabei A, De Vecchis L et al (2012) Hypophysitis induced by monoclonal antibodies to cytotoxic T lymphocyte antigen 4: challenges from a new cause of a rare disease. Oncologist 17:525–535PubMedCentralCrossRefPubMed Torino F, Barnabei A, De Vecchis L et al (2012) Hypophysitis induced by monoclonal antibodies to cytotoxic T lymphocyte antigen 4: challenges from a new cause of a rare disease. Oncologist 17:525–535PubMedCentralCrossRefPubMed
14.
go back to reference Shimatsu A, Oki Y, Fujisawa I, Sano T (2009) Pituitary and stalk lesions (infundibulo-hypophysitis) associated with immunoglobulin G4-related systemic disease: an emerging clinical entity. Endocr J 56:1033–1041CrossRefPubMed Shimatsu A, Oki Y, Fujisawa I, Sano T (2009) Pituitary and stalk lesions (infundibulo-hypophysitis) associated with immunoglobulin G4-related systemic disease: an emerging clinical entity. Endocr J 56:1033–1041CrossRefPubMed
15.
go back to reference Van der Vliet HJJ, Perenboom RM (2004) Multiple pseudotumors in IgG4-associated multifocal systemic fibrosis. Ann Intern Med 141:896–897CrossRefPubMed Van der Vliet HJJ, Perenboom RM (2004) Multiple pseudotumors in IgG4-associated multifocal systemic fibrosis. Ann Intern Med 141:896–897CrossRefPubMed
16.
go back to reference Wong S, Lam WY, Wong WK, Lee KC (2007) Hypophysitis presented as inflammatory pseudotumor in immunoglobulin G4-related systemic disease. Hum Pathol 38:1720–1723CrossRefPubMed Wong S, Lam WY, Wong WK, Lee KC (2007) Hypophysitis presented as inflammatory pseudotumor in immunoglobulin G4-related systemic disease. Hum Pathol 38:1720–1723CrossRefPubMed
17.
go back to reference Bando H, Iguchi G, Fukuoka H et al (2014) The prevalence of IgG4-related hypophysitis in 170 consecutive patients with hypopituitarism and/or central diabetes insipidus and review of the literature. Eur J Endocrinol Eur Fed Endocr Soc 170:161–172CrossRef Bando H, Iguchi G, Fukuoka H et al (2014) The prevalence of IgG4-related hypophysitis in 170 consecutive patients with hypopituitarism and/or central diabetes insipidus and review of the literature. Eur J Endocrinol Eur Fed Endocr Soc 170:161–172CrossRef
18.
go back to reference Honegger J, Fahlbusch R, Bornemann A et al (1997) Lymphocytic and granulomatous hypophysitis: experience with nine cases. Neurosurgery 40:713–722. Discussion 722–723 Honegger J, Fahlbusch R, Bornemann A et al (1997) Lymphocytic and granulomatous hypophysitis: experience with nine cases. Neurosurgery 40:713–722. Discussion 722–723
19.
go back to reference Leung GKK, Lopes M-BS, Thorner MO et al (2004) Primary hypophysitis: a single-center experience in 16 cases. J Neurosurg 101:262–271CrossRefPubMed Leung GKK, Lopes M-BS, Thorner MO et al (2004) Primary hypophysitis: a single-center experience in 16 cases. J Neurosurg 101:262–271CrossRefPubMed
20.
go back to reference Gutenberg A, Hans V, Puchner MJA et al (2006) Primary hypophysitis: clinical-pathological correlations. Eur J Endocrinol Eur Fed Endocr Soc 155:101–107CrossRef Gutenberg A, Hans V, Puchner MJA et al (2006) Primary hypophysitis: clinical-pathological correlations. Eur J Endocrinol Eur Fed Endocr Soc 155:101–107CrossRef
21.
go back to reference Menon SK, Sarathi V, Bandgar TR et al (2009) Autoimmune hypophysitis: a single centre experience. Singap Med J 50:1080–1084 Menon SK, Sarathi V, Bandgar TR et al (2009) Autoimmune hypophysitis: a single centre experience. Singap Med J 50:1080–1084
22.
go back to reference Gutenberg A, Larsen J, Lupi I et al (2009) A radiologic Score to distinguish autoimmune hypophysitis from nonsecreting pituitary adenoma preoperatively. Am J Neuroradiol 30:1766–1772CrossRefPubMed Gutenberg A, Larsen J, Lupi I et al (2009) A radiologic Score to distinguish autoimmune hypophysitis from nonsecreting pituitary adenoma preoperatively. Am J Neuroradiol 30:1766–1772CrossRefPubMed
23.
go back to reference Leporati P, Landek-Salgado MA, Lupi I et al (2011) IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab 96:1971–1980PubMedCentralCrossRefPubMed Leporati P, Landek-Salgado MA, Lupi I et al (2011) IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab 96:1971–1980PubMedCentralCrossRefPubMed
24.
go back to reference Umehara H, Okazaki K, Masaki Y et al (2012) Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol Jpn Rheum Assoc 22:21–30CrossRef Umehara H, Okazaki K, Masaki Y et al (2012) Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol Jpn Rheum Assoc 22:21–30CrossRef
25.
go back to reference Asa SL, Bilbao JM, Kovacs K et al (1981) Lymphocytic hypophysitis of pregnancy resulting in hypopituitarism: a distinct clinicopathologic entity. Ann Intern Med 95:166–171CrossRefPubMed Asa SL, Bilbao JM, Kovacs K et al (1981) Lymphocytic hypophysitis of pregnancy resulting in hypopituitarism: a distinct clinicopathologic entity. Ann Intern Med 95:166–171CrossRefPubMed
26.
go back to reference Landek-Salgado MA, Gutenberg A, Lupi I et al (2010) Pregnancy, postpartum autoimmune thyroiditis, and autoimmune hypophysitis: intimate relationships. Autoimmun Rev 9:153–157PubMedCentralCrossRefPubMed Landek-Salgado MA, Gutenberg A, Lupi I et al (2010) Pregnancy, postpartum autoimmune thyroiditis, and autoimmune hypophysitis: intimate relationships. Autoimmun Rev 9:153–157PubMedCentralCrossRefPubMed
27.
go back to reference Sautner D, Saeger W, Lüdecke DK et al (1995) Hypophysitis in surgical and autoptical specimens. Acta Neuropathol (Berl) 90:637–644CrossRef Sautner D, Saeger W, Lüdecke DK et al (1995) Hypophysitis in surgical and autoptical specimens. Acta Neuropathol (Berl) 90:637–644CrossRef
28.
go back to reference Fehn M, Sommer C, Ludecke DK et al (1998) Lymphocytic hypophysitis: light and electron microscopic findings and correlation to clinical appearance. Endocr Pathol 9:71–78CrossRefPubMed Fehn M, Sommer C, Ludecke DK et al (1998) Lymphocytic hypophysitis: light and electron microscopic findings and correlation to clinical appearance. Endocr Pathol 9:71–78CrossRefPubMed
29.
go back to reference Buxton N, Robertson I (2001) Lymphocytic and granulocytic hypophysitis: a single centre experience. Br J Neurosurg 15:242–245. Discussion 245–246 Buxton N, Robertson I (2001) Lymphocytic and granulocytic hypophysitis: a single centre experience. Br J Neurosurg 15:242–245. Discussion 245–246
30.
go back to reference Yamamoto M, Takahashi H, Ohara M et al (2006) A case of Mikulicz’s disease (IgG4-related plasmacytic disease) complicated by autoimmune hypophysitis. Scand J Rheumatol 35:410–411CrossRefPubMed Yamamoto M, Takahashi H, Ohara M et al (2006) A case of Mikulicz’s disease (IgG4-related plasmacytic disease) complicated by autoimmune hypophysitis. Scand J Rheumatol 35:410–411CrossRefPubMed
31.
go back to reference Zen Y, Kitagawa S, Minato H et al (2005) IgG4-positive plasma cells in inflammatory pseudotumor (plasma cell granuloma) of the lung. Hum Pathol 36:710–717CrossRefPubMed Zen Y, Kitagawa S, Minato H et al (2005) IgG4-positive plasma cells in inflammatory pseudotumor (plasma cell granuloma) of the lung. Hum Pathol 36:710–717CrossRefPubMed
32.
go back to reference Fujiu K, Sakuma H, Miyamoto H, Yamaguchi B (2010) Immunoglobulin G4-related inflammatory pseudotumor of the lung. Gen Thorac Cardiovasc Surg 58:144–148CrossRefPubMed Fujiu K, Sakuma H, Miyamoto H, Yamaguchi B (2010) Immunoglobulin G4-related inflammatory pseudotumor of the lung. Gen Thorac Cardiovasc Surg 58:144–148CrossRefPubMed
33.
go back to reference Nishikawa G, Nakamura K, Yamada Y et al (2011) Inflammatory pseudotumors of the kidney and the lung presenting as immunoglobulin G4-related disease: a case report. J Med Case Rep 5:480PubMedCentralCrossRefPubMed Nishikawa G, Nakamura K, Yamada Y et al (2011) Inflammatory pseudotumors of the kidney and the lung presenting as immunoglobulin G4-related disease: a case report. J Med Case Rep 5:480PubMedCentralCrossRefPubMed
34.
go back to reference Albini CH, MacGillivray MH, Fisher JE et al (1988) Triad of hypopituitarism, granulomatous hypophysitis, and ruptured Rathke’s cleft cyst. Neurosurgery 22:133–136PubMed Albini CH, MacGillivray MH, Fisher JE et al (1988) Triad of hypopituitarism, granulomatous hypophysitis, and ruptured Rathke’s cleft cyst. Neurosurgery 22:133–136PubMed
35.
go back to reference Wearne MJ, Barber PC, Johnson AP (1995) Symptomatic Rathke’s cleft cyst with hypophysitis. Br J Neurosurg 9:799–803CrossRefPubMed Wearne MJ, Barber PC, Johnson AP (1995) Symptomatic Rathke’s cleft cyst with hypophysitis. Br J Neurosurg 9:799–803CrossRefPubMed
36.
go back to reference Roncaroli F, Bacci A, Frank G, Calbucci F (1998) Granulomatous hypophysitis caused by a ruptured intrasellar Rathke’s cleft cyst: report of a case and review of the literature. Neurosurgery 43:146–149CrossRefPubMed Roncaroli F, Bacci A, Frank G, Calbucci F (1998) Granulomatous hypophysitis caused by a ruptured intrasellar Rathke’s cleft cyst: report of a case and review of the literature. Neurosurgery 43:146–149CrossRefPubMed
37.
go back to reference Hama S, Arita K, Tominaga A et al (1999) Symptomatic Rathke’s cleft cyst coexisting with central diabetes insipidus and hypophysitis: case report. Endocr J 46:187–192CrossRefPubMed Hama S, Arita K, Tominaga A et al (1999) Symptomatic Rathke’s cleft cyst coexisting with central diabetes insipidus and hypophysitis: case report. Endocr J 46:187–192CrossRefPubMed
38.
go back to reference Daikokuya H, Inoue Y, Nemoto Y et al (2000) Rathke’s cleft cyst associated with hypophysitis: MRI. Neuroradiology 42:532–534CrossRefPubMed Daikokuya H, Inoue Y, Nemoto Y et al (2000) Rathke’s cleft cyst associated with hypophysitis: MRI. Neuroradiology 42:532–534CrossRefPubMed
39.
go back to reference Nishikawa T, Takahashi JA, Shimatsu A, Hashimoto N (2007) Hypophysitis caused by Rathke’s cleft cyst case report. Neurol Med Chir (Tokyo) 47:136–139CrossRef Nishikawa T, Takahashi JA, Shimatsu A, Hashimoto N (2007) Hypophysitis caused by Rathke’s cleft cyst case report. Neurol Med Chir (Tokyo) 47:136–139CrossRef
40.
go back to reference Komatsu F, Tsugu H, Komatsu M et al (2010) Clinicopathological characteristics in patients presenting with acute onset of symptoms caused by Rathke’s cleft cysts. Acta Neurochir (Wien) 152:1673–1678CrossRef Komatsu F, Tsugu H, Komatsu M et al (2010) Clinicopathological characteristics in patients presenting with acute onset of symptoms caused by Rathke’s cleft cysts. Acta Neurochir (Wien) 152:1673–1678CrossRef
41.
go back to reference Myers JL, Kurtin PJ, Katzenstein AL et al (1995) Lymphomatoid granulomatosis. Evidence of immunophenotypic diversity and relationship to Epstein–Barr virus infection. Am J Surg Pathol 19:1300–1312CrossRefPubMed Myers JL, Kurtin PJ, Katzenstein AL et al (1995) Lymphomatoid granulomatosis. Evidence of immunophenotypic diversity and relationship to Epstein–Barr virus infection. Am J Surg Pathol 19:1300–1312CrossRefPubMed
42.
go back to reference Jaffe ES, Wilson WH (1997) Lymphomatoid granulomatosis: pathogenesis, pathology and clinical implications. Cancer Surv 30:233–248PubMed Jaffe ES, Wilson WH (1997) Lymphomatoid granulomatosis: pathogenesis, pathology and clinical implications. Cancer Surv 30:233–248PubMed
43.
go back to reference Roschewski M, Wilson WH (2012) Lymphomatoid granulomatosis. Cancer J Sudbury Mass 18:469–474CrossRef Roschewski M, Wilson WH (2012) Lymphomatoid granulomatosis. Cancer J Sudbury Mass 18:469–474CrossRef
44.
go back to reference Tagliavini E, Rossi G, Valli R et al (2013) Lymphomatoid granulomatosis: a practical review for pathologists dealing with this rare pulmonary lymphoproliferative process. Pathologica 105:111–116PubMed Tagliavini E, Rossi G, Valli R et al (2013) Lymphomatoid granulomatosis: a practical review for pathologists dealing with this rare pulmonary lymphoproliferative process. Pathologica 105:111–116PubMed
45.
go back to reference Katzenstein AL, Carrington CB, Liebow AA (1979) Lymphomatoid granulomatosis: a clinicopathologic study of 152 cases. Cancer 43:360–373CrossRefPubMed Katzenstein AL, Carrington CB, Liebow AA (1979) Lymphomatoid granulomatosis: a clinicopathologic study of 152 cases. Cancer 43:360–373CrossRefPubMed
46.
go back to reference Patsalides AD, Atac G, Hedge U et al (2005) Lymphomatoid granulomatosis: abnormalities of the brain at MR imaging. Radiology 237:265–273CrossRefPubMed Patsalides AD, Atac G, Hedge U et al (2005) Lymphomatoid granulomatosis: abnormalities of the brain at MR imaging. Radiology 237:265–273CrossRefPubMed
47.
go back to reference Bushunow PW, Casas V, Duggan DB (1996) Lyphomatoid granulomatosis causing central diabetes insipidus: case report and review of the literature. Cancer Invest 14:112–119CrossRefPubMed Bushunow PW, Casas V, Duggan DB (1996) Lyphomatoid granulomatosis causing central diabetes insipidus: case report and review of the literature. Cancer Invest 14:112–119CrossRefPubMed
48.
go back to reference Carmichael JD (2012) Update on the diagnosis and management of hypophysitis. Curr Opin Endocrinol Diabetes Obes 19:314–321CrossRefPubMed Carmichael JD (2012) Update on the diagnosis and management of hypophysitis. Curr Opin Endocrinol Diabetes Obes 19:314–321CrossRefPubMed
49.
go back to reference Lecube A, Francisco G, Rodríguez D et al (2003) Lymphocytic hypophysitis successfully treated with azathioprine: first case report. J Neurol Neurosurg Psychiatry 74:1581–1583PubMedCentralCrossRefPubMed Lecube A, Francisco G, Rodríguez D et al (2003) Lymphocytic hypophysitis successfully treated with azathioprine: first case report. J Neurol Neurosurg Psychiatry 74:1581–1583PubMedCentralCrossRefPubMed
50.
go back to reference Curtò L, Torre ML, Cotta OR et al (2010) Lymphocytic hypophysitis: differential diagnosis and effects of high-dose pulse steroids, followed by azathioprine, on the pituitary mass and endocrine abnormalities—report of a case and literature review. Sci World J 10:126–134CrossRef Curtò L, Torre ML, Cotta OR et al (2010) Lymphocytic hypophysitis: differential diagnosis and effects of high-dose pulse steroids, followed by azathioprine, on the pituitary mass and endocrine abnormalities—report of a case and literature review. Sci World J 10:126–134CrossRef
51.
go back to reference Lu Z, Yang G, Ba J et al (2011) Spontaneous pregnancy in a patient with a relapse of lymphocytic hypophysitis successfully treated with azathioprine and glucocorticoids. Endocrine 39:296–297CrossRefPubMed Lu Z, Yang G, Ba J et al (2011) Spontaneous pregnancy in a patient with a relapse of lymphocytic hypophysitis successfully treated with azathioprine and glucocorticoids. Endocrine 39:296–297CrossRefPubMed
52.
go back to reference Papanastasiou L, Pappa T, Tsiavos V et al (2011) Azathioprine as an alternative treatment in primary hypophysitis. Pituitary 14:16–22CrossRefPubMed Papanastasiou L, Pappa T, Tsiavos V et al (2011) Azathioprine as an alternative treatment in primary hypophysitis. Pituitary 14:16–22CrossRefPubMed
53.
go back to reference Yang G-Q, Lu Z-H, Gu W-J et al (2011) Recurrent autoimmune hypophysitis successfully treated with glucocorticoids plus azathioprine: a report of three cases. Endocr J 58:675–683CrossRefPubMed Yang G-Q, Lu Z-H, Gu W-J et al (2011) Recurrent autoimmune hypophysitis successfully treated with glucocorticoids plus azathioprine: a report of three cases. Endocr J 58:675–683CrossRefPubMed
54.
go back to reference Caputo C, Bazargan A, McKelvie PA et al (2014) Hypophysitis due to IgG4-related disease responding to treatment with azathioprine: an alternative to corticosteroid therapy. Pituitary 17:251–256CrossRefPubMed Caputo C, Bazargan A, McKelvie PA et al (2014) Hypophysitis due to IgG4-related disease responding to treatment with azathioprine: an alternative to corticosteroid therapy. Pituitary 17:251–256CrossRefPubMed
55.
go back to reference Schreckinger M, Francis T, Rajah G et al (2012) Novel strategy to treat a case of recurrent lymphocytic hypophysitis using rituximab. J Neurosurg 116:1318–1323CrossRefPubMed Schreckinger M, Francis T, Rajah G et al (2012) Novel strategy to treat a case of recurrent lymphocytic hypophysitis using rituximab. J Neurosurg 116:1318–1323CrossRefPubMed
56.
go back to reference Selch MT, DeSalles AAF, Kelly DF et al (2003) Stereotactic radiotherapy for the treatment of lymphocytic hypophysitis: report of two cases. J Neurosurg 99:591–596CrossRefPubMed Selch MT, DeSalles AAF, Kelly DF et al (2003) Stereotactic radiotherapy for the treatment of lymphocytic hypophysitis: report of two cases. J Neurosurg 99:591–596CrossRefPubMed
57.
go back to reference Ray DK, Yen CP, Vance ML et al (2010) Gamma knife surgery for lymphocytic hypophysitis. J Neurosurg 112:118–121CrossRefPubMed Ray DK, Yen CP, Vance ML et al (2010) Gamma knife surgery for lymphocytic hypophysitis. J Neurosurg 112:118–121CrossRefPubMed
58.
go back to reference Howlett TA, Levy MJ, Robertson IJ (2010) How reliably can autoimmune hypophysitis be diagnosed without pituitary biopsy. Clin Endocrinol (Oxf) 73:18–21 Howlett TA, Levy MJ, Robertson IJ (2010) How reliably can autoimmune hypophysitis be diagnosed without pituitary biopsy. Clin Endocrinol (Oxf) 73:18–21
59.
go back to reference Swearingen B, Barker FG 2nd, Katznelson L et al (1998) Long-term mortality after transsphenoidal surgery and adjunctive therapy for acromegaly. J Clin Endocrinol Metab 83:3419–3426PubMed Swearingen B, Barker FG 2nd, Katznelson L et al (1998) Long-term mortality after transsphenoidal surgery and adjunctive therapy for acromegaly. J Clin Endocrinol Metab 83:3419–3426PubMed
60.
go back to reference Jahangiri A, Wagner JR, Pekmezci M et al (2013) A comprehensive long-term retrospective analysis of silent corticotrophic adenomas vs hormone-negative adenomas. Neurosurgery 73:8–17. Discussion 17–18 Jahangiri A, Wagner JR, Pekmezci M et al (2013) A comprehensive long-term retrospective analysis of silent corticotrophic adenomas vs hormone-negative adenomas. Neurosurgery 73:8–17. Discussion 17–18
61.
go back to reference Jahangiri A, Wagner J, Han SW et al (2014) Morbidity of repeat transsphenoidal surgery assessed in more than 1000 operations. J Neurosurg 121:67–74 Jahangiri A, Wagner J, Han SW et al (2014) Morbidity of repeat transsphenoidal surgery assessed in more than 1000 operations. J Neurosurg 121:67–74
Metadata
Title
Hypophysitis: a single-center case series
Authors
Brandon S. Imber
Han S. Lee
Sandeep Kunwar
Lewis S. Blevins
Manish K. Aghi
Publication date
01-10-2015
Publisher
Springer US
Published in
Pituitary / Issue 5/2015
Print ISSN: 1386-341X
Electronic ISSN: 1573-7403
DOI
https://doi.org/10.1007/s11102-014-0622-5

Other articles of this Issue 5/2015

Pituitary 5/2015 Go to the issue