Skip to main content
Top
Published in: Endocrine 3/2019

01-03-2019 | Endocrine Surgery

High prevalence of adrenal insufficiency at diagnosis and headache recovery in surgically resected Rathke’s cleft cysts—a large retrospective single center study

Authors: Fabienne Langlois, Anamaria Manea, Dawn Shao Ting Lim, Shirley McCartney, Christine G. Yedinak, Justin S. Cetas, Maria Fleseriu

Published in: Endocrine | Issue 3/2019

Login to get access

Abstract

Background

Rathke’s cleft cysts (RCC) are lesions that arise from Rathke’s pouch. Though frequently incidental, resulting symptoms in a minority of cases are indicators for surgical resection, which may prove beneficial.

Objective

To characterize a cohort of surgically-resected RCC cases at Oregon Health & Science University; tabulate associated hormonal imbalances and symptoms, possible symptom reversal with surgery, determine recurrence risk; identify predictors of recurrence and headache improvement.

Method

Electronic records of all RCC resected cases (from 2006–2016; 11 years) were retrospectively reviewed. Patients had been evaluated by one neuroendocrinologist using a uniform protocol.

Results

A pathological RCC diagnosis was established in 73 of 814 (9%) surgical pituitary cases. The RCC cohort was 77% (n = 56/73) female, mean age was 39.5 ± 14.9 years at first surgery, and at presentation headache was reported in 88% and visual defects/diplopia in 18% of patients. Initial RCC maximum diameter was 1.3 ± 0.7 cm. The most frequent hormonal deficit was cortisol; 24% of patients had a new adrenal insufficiency (AI) diagnosis, however, 36% also had AI at 3 months post-operatively. Mean follow up was 4.0 ± 4.5 years. Two-thirds of patients (41/62) had headache improvement 3 months post-operatively. Post-operative imaging revealed no residual cyst in 58% (38/65). In those patients with no residual RCC, 29% had recurrence and 71% had long lasting cure. From the 42% (27/65) of patients with residual cyst on post-operative imaging; 59% (16/27) remained stable, 26% (7/27) progressed and 15% (4/27) regressed.

Conclusion

Symptomatic RCC present mostly in women, with a high proportion reporting headaches. Prevalence of AI at diagnosis is high. Surgery may not achieve adrenal axis recovery, but renders a high percentage of headache improvement. Approximately 25% of RCC will recur by 4 years postoperatively. Clinicians should cautiously screen patients with symptomatic RCC, regardless of lesion size for AI.
Literature
1.
go back to reference C.J. Aho, C. Liu, V. Zelman, W.T. Couldwell, M.H. Weiss, Surgical outcomes in 118 patients with Rathke cleft cysts. J. Neurosurg. 102, 189–193 (2005)CrossRefPubMed C.J. Aho, C. Liu, V. Zelman, W.T. Couldwell, M.H. Weiss, Surgical outcomes in 118 patients with Rathke cleft cysts. J. Neurosurg. 102, 189–193 (2005)CrossRefPubMed
2.
go back to reference R. Trifanescu, V. Stavrinides, P. Plaha, S. Cudlip, J.V. Byrne, O. Ansorge, J.A. Wass, N. Karavitaki, Outcome in surgically treated Rathke’s cleft cysts: long-term monitoring needed. Eur. J. Endocrinol. 165, 33–37 (2011)CrossRefPubMed R. Trifanescu, V. Stavrinides, P. Plaha, S. Cudlip, J.V. Byrne, O. Ansorge, J.A. Wass, N. Karavitaki, Outcome in surgically treated Rathke’s cleft cysts: long-term monitoring needed. Eur. J. Endocrinol. 165, 33–37 (2011)CrossRefPubMed
3.
go back to reference G. Childs, Pituitary Gland (Cell Types, Mediators, Development), in Squire L (ed): Encyclopedia of Neuroscience. California: Academic Press 2009, Vol 7, pp 719–726 G. Childs, Pituitary Gland (Cell Types, Mediators, Development), in Squire L (ed): Encyclopedia of Neuroscience. California: Academic Press 2009, Vol 7, pp 719–726
4.
go back to reference E. Kim, Symptomatic Rathke cleft cyst: clinical features and surgical outcomes. World Neurosurg. 78, 527–534 (2012)CrossRefPubMed E. Kim, Symptomatic Rathke cleft cyst: clinical features and surgical outcomes. World Neurosurg. 78, 527–534 (2012)CrossRefPubMed
5.
go back to reference S.A. Culver, Y. Grober, D.A. Ornan, J.T. Patrie, E.H. Oldfield, J.A. Jane Jr., M.O. Thorner, A case for conservative management: characterizing the natural history of radiographically diagnosed Rathke cleft cysts. J. Clin. Endocrinol. Metab. 100, 3943–3948 (2015)CrossRefPubMedPubMedCentral S.A. Culver, Y. Grober, D.A. Ornan, J.T. Patrie, E.H. Oldfield, J.A. Jane Jr., M.O. Thorner, A case for conservative management: characterizing the natural history of radiographically diagnosed Rathke cleft cysts. J. Clin. Endocrinol. Metab. 100, 3943–3948 (2015)CrossRefPubMedPubMedCentral
6.
go back to reference V. Vasilev, L. Rostomyan, A.F. Daly, I. Potorac, S. Zacharieva, J.F. Bonneville, A. Beckers, Management of endocrine disease: pituitary “incidentaloma”: neuroradiological assessment and differential diagnosis. Eur. J. Endocrinol. 175, R171–184 (2016)CrossRefPubMed V. Vasilev, L. Rostomyan, A.F. Daly, I. Potorac, S. Zacharieva, J.F. Bonneville, A. Beckers, Management of endocrine disease: pituitary “incidentaloma”: neuroradiological assessment and differential diagnosis. Eur. J. Endocrinol. 175, R171–184 (2016)CrossRefPubMed
7.
go back to reference P.U. Freda, A.M. Beckers, L. Katznelson, M.E. Molitch, V.M. Montori, K.D. Post, M.L. Vance, S. Endocrine, Pituitary incidentaloma: an endocrine society clinical practice guideline. J. Clin. Endocrinol. Metab. 96, 894–904 (2011)CrossRefPubMedPubMedCentral P.U. Freda, A.M. Beckers, L. Katznelson, M.E. Molitch, V.M. Montori, K.D. Post, M.L. Vance, S. Endocrine, Pituitary incidentaloma: an endocrine society clinical practice guideline. J. Clin. Endocrinol. Metab. 96, 894–904 (2011)CrossRefPubMedPubMedCentral
8.
go back to reference R. Trifanescu, O. Ansorge, J.A. Wass, A.B. Grossman, N. Karavitaki, Rathke’s cleft cysts. Clin. Endocrinol. (Oxf.) 76, 151–160 (2012)CrossRef R. Trifanescu, O. Ansorge, J.A. Wass, A.B. Grossman, N. Karavitaki, Rathke’s cleft cysts. Clin. Endocrinol. (Oxf.) 76, 151–160 (2012)CrossRef
9.
go back to reference J.L. Shin, S.L. Asa, L.J. Woodhouse, H.S. Smyth, S. Ezzat, Cystic lesions of the pituitary: clinicopathological features distinguishing craniopharyngioma, Rathke’s cleft cyst, and arachnoid cyst. J. Clin. Endocrinol. Metab. 84, 3972–3982 (1999)PubMed J.L. Shin, S.L. Asa, L.J. Woodhouse, H.S. Smyth, S. Ezzat, Cystic lesions of the pituitary: clinicopathological features distinguishing craniopharyngioma, Rathke’s cleft cyst, and arachnoid cyst. J. Clin. Endocrinol. Metab. 84, 3972–3982 (1999)PubMed
10.
go back to reference M.E. Molitch, D.R. Clemmons, S. Malozowski, G.R. Merriam, M.L. Vance, S. Endocrine, Evaluation and treatment of adult growth hormone deficiency: an Endocrine Society clinical practice guideline. J. Clin. Endocrinol. Metab. 96, 1587–1609 (2011)CrossRefPubMed M.E. Molitch, D.R. Clemmons, S. Malozowski, G.R. Merriam, M.L. Vance, S. Endocrine, Evaluation and treatment of adult growth hormone deficiency: an Endocrine Society clinical practice guideline. J. Clin. Endocrinol. Metab. 96, 1587–1609 (2011)CrossRefPubMed
11.
go back to reference M. Fleseriu, I.A. Hashim, N. Karavitaki, S. Melmed, M.H. Murad, R. Salvatori, M.H. Samuels, Hormonal replacement in hypopituitarism in adults: an Endocrine Society Clinical Practice Guideline. J. Clin. Endocrinol. Metab. 101, 3888–3921 (2016)CrossRefPubMed M. Fleseriu, I.A. Hashim, N. Karavitaki, S. Melmed, M.H. Murad, R. Salvatori, M.H. Samuels, Hormonal replacement in hypopituitarism in adults: an Endocrine Society Clinical Practice Guideline. J. Clin. Endocrinol. Metab. 101, 3888–3921 (2016)CrossRefPubMed
12.
go back to reference L. Wen, L.B. Hu, X.Y. Feng, G. Desai, L.G. Zou, W.X. Wang, D. Zhang, Rathke’s cleft cyst: clinicopathological and MRI findings in 22 patients. Clin. Radiol. 65, 47–55 (2010)CrossRefPubMed L. Wen, L.B. Hu, X.Y. Feng, G. Desai, L.G. Zou, W.X. Wang, D. Zhang, Rathke’s cleft cyst: clinicopathological and MRI findings in 22 patients. Clin. Radiol. 65, 47–55 (2010)CrossRefPubMed
13.
go back to reference E. Sala, J.M. Moore, A. Amorin, G. Carosi, H. Martinez Jr., G.R. Harsh, M. Arosio, G.Mantovani, L. Katznelson, Natural history of Rathke's cleft cysts: a retrospective analysis of a two centers experience. Clin. Endocrinol. 89, 178–186 (2018).CrossRef E. Sala, J.M. Moore, A. Amorin, G. Carosi, H. Martinez Jr., G.R. Harsh, M. Arosio, G.Mantovani, L. Katznelson, Natural history of Rathke's cleft cysts: a retrospective analysis of a two centers experience. Clin. Endocrinol. 89, 178–186 (2018).CrossRef
14.
go back to reference R.J. Benveniste, W.A. King, J. Walsh, J.S. Lee, T.P. Naidich, K.D. Post, Surgery for Rathke cleft cysts: technical considerations and outcomes. J. Neurosurg. 101, 577–584 (2004)CrossRefPubMed R.J. Benveniste, W.A. King, J. Walsh, J.S. Lee, T.P. Naidich, K.D. Post, Surgery for Rathke cleft cysts: technical considerations and outcomes. J. Neurosurg. 101, 577–584 (2004)CrossRefPubMed
15.
go back to reference P. Cohan, A. Foulad, F. Esposito, N.A. Martin, D.F. Kelly, Symptomatic Rathke’s cleft cysts: a report of 24 cases. J. Endocrinol. Invest. 27, 943–948 (2004)CrossRefPubMed P. Cohan, A. Foulad, F. Esposito, N.A. Martin, D.F. Kelly, Symptomatic Rathke’s cleft cysts: a report of 24 cases. J. Endocrinol. Invest. 27, 943–948 (2004)CrossRefPubMed
16.
go back to reference H. Nishioka, J. Haraoka, H. Izawa, Y. Ikeda, Headaches associated with Rathke’s cleft cyst. Headache 46, 1580–1586 (2006)CrossRefPubMed H. Nishioka, J. Haraoka, H. Izawa, Y. Ikeda, Headaches associated with Rathke’s cleft cyst. Headache 46, 1580–1586 (2006)CrossRefPubMed
18.
go back to reference V. Ratha, S. Patil, V.S. Karmarkar, N.J. Shah, C.E. Deopujari, Surgical management of Rathke cleft cysts. World Neurosurg. 107, 276–284 (2017)CrossRefPubMed V. Ratha, S. Patil, V.S. Karmarkar, N.J. Shah, C.E. Deopujari, Surgical management of Rathke cleft cysts. World Neurosurg. 107, 276–284 (2017)CrossRefPubMed
19.
go back to reference E. Kim, Surgical treatment of symptomatic Rathke cleft cysts clinical features and results with special attention to recurrence. J. Neurosurg. 100, 33–40 (2004)CrossRefPubMed E. Kim, Surgical treatment of symptomatic Rathke cleft cysts clinical features and results with special attention to recurrence. J. Neurosurg. 100, 33–40 (2004)CrossRefPubMed
20.
go back to reference W. Zhong, C. You, S. Jiang, S. Huang, H. Chen, J. Liu, P. Zhou, Y. Liu, B. Cai, Symptomatic Rathke cleft cyst. J. Clin. Neurosci. 19, 501–508 (2012)CrossRefPubMed W. Zhong, C. You, S. Jiang, S. Huang, H. Chen, J. Liu, P. Zhou, Y. Liu, B. Cai, Symptomatic Rathke cleft cyst. J. Clin. Neurosci. 19, 501–508 (2012)CrossRefPubMed
21.
go back to reference S. Chotai, Y. Liu, J. Pan, S. Qi, Characteristics of Rathke’s cleft cyst based on cyst location with a primary focus on recurrence after resection. J. Neurosurg. 122, 1380–1389 (2015)CrossRefPubMed S. Chotai, Y. Liu, J. Pan, S. Qi, Characteristics of Rathke’s cleft cyst based on cyst location with a primary focus on recurrence after resection. J. Neurosurg. 122, 1380–1389 (2015)CrossRefPubMed
22.
go back to reference F. Langlois, D.S.T. Lim, C.G. Yedinak, I. Cetas, S. McCartney, J. Cetas, A. Dogan, M. Fleseriu, Predictors of silent corticotroph adenoma recurrence; a large retrospective single center study and systematic literature review. Pituitary 21, 32–40 (2018)CrossRefPubMed F. Langlois, D.S.T. Lim, C.G. Yedinak, I. Cetas, S. McCartney, J. Cetas, A. Dogan, M. Fleseriu, Predictors of silent corticotroph adenoma recurrence; a large retrospective single center study and systematic literature review. Pituitary 21, 32–40 (2018)CrossRefPubMed
23.
go back to reference K. Tanigawa, S. Yamashita, H. Namba, M.C. Villadolid, H. Kimura, T. Tominaga, M. Tsuruta, N. Yokoyama, M. Izumi, S. Nagataki, Acute adrenal insufficiency due to symptomatic Rathke’s cleft cyst. Intern. Med. 31, 467–469 (1992)CrossRefPubMed K. Tanigawa, S. Yamashita, H. Namba, M.C. Villadolid, H. Kimura, T. Tominaga, M. Tsuruta, N. Yokoyama, M. Izumi, S. Nagataki, Acute adrenal insufficiency due to symptomatic Rathke’s cleft cyst. Intern. Med. 31, 467–469 (1992)CrossRefPubMed
24.
go back to reference Y. Hirayama, T. Kudo, N. Kasai, Acute adrenal insufficiency associated with Rathke’s cleft cyst. Intern. Med. 55, 639–642 (2016)CrossRefPubMed Y. Hirayama, T. Kudo, N. Kasai, Acute adrenal insufficiency associated with Rathke’s cleft cyst. Intern. Med. 55, 639–642 (2016)CrossRefPubMed
25.
go back to reference C. Janeczko, J. McHugh, D. Rawluk, M. Farrell, P. Brennan, N. Delanty, Hypophysitis secondary to ruptured Rathke’s cyst mimicking neurosarcoidosis. J. Clin. Neurosci. 16, 599–600 (2009)CrossRefPubMed C. Janeczko, J. McHugh, D. Rawluk, M. Farrell, P. Brennan, N. Delanty, Hypophysitis secondary to ruptured Rathke’s cyst mimicking neurosarcoidosis. J. Clin. Neurosci. 16, 599–600 (2009)CrossRefPubMed
26.
go back to reference Y. Hayashi, M. Oishi, D. Kita, T. Watanabe, O. Tachibana, J. Hamada, Pure lymphocytic infundibuloneurohypophysitis caused by the rupture of Rathke’s cleft cyst: report of 2 cases and review of the literature. Turk. Neurosurg. 25, 332–336 (2015)PubMed Y. Hayashi, M. Oishi, D. Kita, T. Watanabe, O. Tachibana, J. Hamada, Pure lymphocytic infundibuloneurohypophysitis caused by the rupture of Rathke’s cleft cyst: report of 2 cases and review of the literature. Turk. Neurosurg. 25, 332–336 (2015)PubMed
27.
go back to reference M. Asakawa, R. Chin, Y. Niitsu, T. Sekine, A. Niwa, A. Miyake, N. Inoshita, M. Kawamura, Y. Ogawa, Y. Hirata, A case of Rathke’s cleft cyst associated with transient central adrenal insufficiency and masked diabetes insipidus. Case Rep. Endocrinol. 2014, 693294 (2014)PubMedPubMedCentral M. Asakawa, R. Chin, Y. Niitsu, T. Sekine, A. Niwa, A. Miyake, N. Inoshita, M. Kawamura, Y. Ogawa, Y. Hirata, A case of Rathke’s cleft cyst associated with transient central adrenal insufficiency and masked diabetes insipidus. Case Rep. Endocrinol. 2014, 693294 (2014)PubMedPubMedCentral
28.
go back to reference F. Komatsu, H. Tsugu, M. Komatsu, S. Sakamoto, S. Oshiro, T. Fukushima, K. Nabeshima, T. Inoue, Clinicopathological characteristics in patients presenting with acute onset of symptoms caused by Rathke’s cleft cysts. Acta Neurochir. 152, 1673–1678 (2010)CrossRefPubMed F. Komatsu, H. Tsugu, M. Komatsu, S. Sakamoto, S. Oshiro, T. Fukushima, K. Nabeshima, T. Inoue, Clinicopathological characteristics in patients presenting with acute onset of symptoms caused by Rathke’s cleft cysts. Acta Neurochir. 152, 1673–1678 (2010)CrossRefPubMed
29.
go back to reference K. Duan, S.L. Asa, D. Winer, Z. Gelareh, F. Gentili, O. Mete, Xanthomatous hypophysitis is associated with ruptured Rathke’s cleft cyst. Endocr. Pathol. 28, 83–90 (2017)CrossRefPubMed K. Duan, S.L. Asa, D. Winer, Z. Gelareh, F. Gentili, O. Mete, Xanthomatous hypophysitis is associated with ruptured Rathke’s cleft cyst. Endocr. Pathol. 28, 83–90 (2017)CrossRefPubMed
30.
go back to reference J. Schittenhelm, R. Beschorner, T. Psaras, D. Capper, T. Nagele, R. Meyermann, W. Saeger, J. Honegger, M. Mittelbronn, Rathke’s cleft cyst rupture as potential initial event of a secondary perifocal lymphocytic hypophysitis: proposal of an unusual pathogenetic event and review of the literature. Neurosurg. Rev. 31, 157–163 (2008)CrossRefPubMed J. Schittenhelm, R. Beschorner, T. Psaras, D. Capper, T. Nagele, R. Meyermann, W. Saeger, J. Honegger, M. Mittelbronn, Rathke’s cleft cyst rupture as potential initial event of a secondary perifocal lymphocytic hypophysitis: proposal of an unusual pathogenetic event and review of the literature. Neurosurg. Rev. 31, 157–163 (2008)CrossRefPubMed
31.
go back to reference F. Bonneville, F. Cattin, K. Marsot-Dupuch, D. Dormont, J.F. Bonneville, J. Chiras, T1 signal hyperintensity in the sellar region: spectrum of findings. Radiographics 26, 93–113 (2006)CrossRefPubMed F. Bonneville, F. Cattin, K. Marsot-Dupuch, D. Dormont, J.F. Bonneville, J. Chiras, T1 signal hyperintensity in the sellar region: spectrum of findings. Radiographics 26, 93–113 (2006)CrossRefPubMed
32.
go back to reference M. Fleseriu, C. Yedinak, C. Campbell, J.B. Delashaw, Significant headache improvement after transsphenoidal surgery in patients with small sellar lesions. J. Neurosurg. 110, 354–358 (2009)CrossRefPubMed M. Fleseriu, C. Yedinak, C. Campbell, J.B. Delashaw, Significant headache improvement after transsphenoidal surgery in patients with small sellar lesions. J. Neurosurg. 110, 354–358 (2009)CrossRefPubMed
33.
go back to reference S.D. Wait, M.P. Garrett, A.S. Little, B.D. Killory, W.L. White, Endocrinopathy, vision, headache, and recurrence after transsphenoidal surgery for Rathke cleft cysts. Neurosurgery 67, 837–843 (2010)CrossRefPubMed S.D. Wait, M.P. Garrett, A.S. Little, B.D. Killory, W.L. White, Endocrinopathy, vision, headache, and recurrence after transsphenoidal surgery for Rathke cleft cysts. Neurosurgery 67, 837–843 (2010)CrossRefPubMed
34.
go back to reference D.J. Cote, B.D. Besasie, M.M. Hulou, S.C. Yan, T.R. Smith, E.R. Laws, Transsphenoidal surgery for Rathke’s cleft cyst can reduce headache severity and frequency. Pituitary 19, 57–64 (2016)CrossRefPubMed D.J. Cote, B.D. Besasie, M.M. Hulou, S.C. Yan, T.R. Smith, E.R. Laws, Transsphenoidal surgery for Rathke’s cleft cyst can reduce headache severity and frequency. Pituitary 19, 57–64 (2016)CrossRefPubMed
35.
go back to reference N. Altuwaijri, D.J. Cote, N. Lamba, W. Albenayan, S.P. Ren, I. Zaghloul, J. Doucette, H.A. Zaidi, R.A. Mekary, T.R. Smith, Headache resolution after Rathke cleft cyst resection: a meta-analysis. World Neurosurg. 111, e764–e772 (2018)CrossRefPubMed N. Altuwaijri, D.J. Cote, N. Lamba, W. Albenayan, S.P. Ren, I. Zaghloul, J. Doucette, H.A. Zaidi, R.A. Mekary, T.R. Smith, Headache resolution after Rathke cleft cyst resection: a meta-analysis. World Neurosurg. 111, e764–e772 (2018)CrossRefPubMed
36.
go back to reference I. Fukui, Y. Hayashi, D. Kita, Y. Sasagawa, M. Oishi, O. Tachibana, M. Nakada, Significant improvement in chronic persistent headaches caused by small Rathke cleft cysts after transsphenoidal surgery. World Neurosurg. 99, 362–368 (2017)CrossRefPubMed I. Fukui, Y. Hayashi, D. Kita, Y. Sasagawa, M. Oishi, O. Tachibana, M. Nakada, Significant improvement in chronic persistent headaches caused by small Rathke cleft cysts after transsphenoidal surgery. World Neurosurg. 99, 362–368 (2017)CrossRefPubMed
37.
go back to reference M.B. Potts, A. Jahangiri, K.R. Lamborn, L.S. Blevins, S. Kunwar, M.K. Aghi, Suprasellar Rathke cleft cysts: clinical presentation and treatment outcomes. Neurosurgery 69, 1058–1068 (2011)PubMed M.B. Potts, A. Jahangiri, K.R. Lamborn, L.S. Blevins, S. Kunwar, M.K. Aghi, Suprasellar Rathke cleft cysts: clinical presentation and treatment outcomes. Neurosurgery 69, 1058–1068 (2011)PubMed
38.
go back to reference K.O. Lillehei, L. Widdel, C.A. Astete, M.E. Wierman, B.K. Kleinschmidt-DeMasters, J.M. Kerr, Transsphenoidal resection of 82 Rathke cleft cysts: limited value of alcohol cauterization in reducing recurrence rates. J. Neurosurg. 114, 310–317 (2011)CrossRefPubMed K.O. Lillehei, L. Widdel, C.A. Astete, M.E. Wierman, B.K. Kleinschmidt-DeMasters, J.M. Kerr, Transsphenoidal resection of 82 Rathke cleft cysts: limited value of alcohol cauterization in reducing recurrence rates. J. Neurosurg. 114, 310–317 (2011)CrossRefPubMed
39.
go back to reference D.M. Higgins, J.J. Van Gompel, T.B. Nippoldt, F.B. Meyer, Symptomatic Rathke cleft cysts: extent of resection and surgical complications. Neurosurg. Focus 31, E2 (2011)CrossRefPubMed D.M. Higgins, J.J. Van Gompel, T.B. Nippoldt, F.B. Meyer, Symptomatic Rathke cleft cysts: extent of resection and surgical complications. Neurosurg. Focus 31, E2 (2011)CrossRefPubMed
40.
go back to reference Y. Ogawa, M. Watanabe, T. Tominaga, Prognostic factors of operated Rathke’s cleft cysts with special reference to re-accumulation and recommended surgical strategy. Acta Neurochir. 153, 2427–2433 (2011)CrossRefPubMed Y. Ogawa, M. Watanabe, T. Tominaga, Prognostic factors of operated Rathke’s cleft cysts with special reference to re-accumulation and recommended surgical strategy. Acta Neurochir. 153, 2427–2433 (2011)CrossRefPubMed
41.
go back to reference J.K. Park, E.J. Lee, S.H. Kim, Optimal surgical approaches for Rathke cleft cyst with consideration of endocrine function. Neurosurgery 70, 250–256 (2012). discussion 256-257PubMed J.K. Park, E.J. Lee, S.H. Kim, Optimal surgical approaches for Rathke cleft cyst with consideration of endocrine function. Neurosurgery 70, 250–256 (2012). discussion 256-257PubMed
42.
go back to reference Y. Kinoshita, A. Tominaga, S. Usui, K. Arita, T. Sakoguchi, K. Sugiyama, K. Kurisu, The long-term recurrence of Rathke’s cleft cysts as predicted by histology but not by surgical procedure. J. Neurosurg. 125, 1002–1007 (2016)CrossRefPubMed Y. Kinoshita, A. Tominaga, S. Usui, K. Arita, T. Sakoguchi, K. Sugiyama, K. Kurisu, The long-term recurrence of Rathke’s cleft cysts as predicted by histology but not by surgical procedure. J. Neurosurg. 125, 1002–1007 (2016)CrossRefPubMed
Metadata
Title
High prevalence of adrenal insufficiency at diagnosis and headache recovery in surgically resected Rathke’s cleft cysts—a large retrospective single center study
Authors
Fabienne Langlois
Anamaria Manea
Dawn Shao Ting Lim
Shirley McCartney
Christine G. Yedinak
Justin S. Cetas
Maria Fleseriu
Publication date
01-03-2019
Publisher
Springer US
Published in
Endocrine / Issue 3/2019
Print ISSN: 1355-008X
Electronic ISSN: 1559-0100
DOI
https://doi.org/10.1007/s12020-018-1784-0

Other articles of this Issue 3/2019

Endocrine 3/2019 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine