The evolution of pituitary cysts in growth hormone-treated children
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Matthew D. Krasnow
, Nicholas A. Krasnow
, Liam McGuirk , Tara P. Patale , Sarah Manely , Emily Sayegh , Benjamin Epstein , Sarriyah A. Hanif , Shilpa Mehta, Michael Tenner
, Javin Schefflein , Hasit Mehta and Richard A. Noto
Abstract
Objectives
We have previously shown that pituitary cysts may affect growth hormone secretion. This study sought to determine cyst evolution during growth hormone treatment in children.
Methods
Forty-nine patients with short stature, a pituitary cyst, and at least two brain MRI scans were included. The percent of the pituitary gland occupied by the cyst (POGO) was calculated, and a cyst with a POGO of ≤15% was considered small, while a POGO >15% was considered large.
Results
Thirty-five cysts were small, and 14 were large. Five of the 35 small cysts grew into large cysts, while 6 of the 14 large cysts shrunk into small cysts. Of 4 cysts that fluctuated between large and small, 3 presented as large and 1 as small. Small cysts experienced greater change in cyst volume (CV) (mean=61.5%) than large cysts (mean=−0.4%). However, large cysts had a greater net change in CV (mean=44.2 mm3) than small cysts (mean=21.0 mm3). Older patients had significantly larger mean pituitary volume than younger patients (435.4 mm3 vs. 317.9 mm3) and significantly larger mean CV than younger patients (77.4 mm3 vs. 45.2 mm3), but there was no significant difference in POGO between groups.
Conclusions
Pituitary cyst size can vary greatly over time. Determination of POGO over time is a useful marker for determining the possibility of a pathologic effect on pituitary function since it factors both cyst and gland volume. Large cysts should be monitored closely, given their extreme, erratic behavior.
Acknowledgments
We thank all the summer research students who assisted in retrieving and analyzing patient data. We also thank our research coordinator Jane Torres for her invaluable assistance.
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Research funding: None declared.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: The requirement for informed consent was waived by the institutional review board of our institution due to the minimal concern, protection, and de-identification of entirely retrospective data.
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Ethical approval: The research related to human use has complied with all the relevant national regulations and institutional policies, is in accordance with the tenets of the Helsinki Declaration, and has been approved by the Institutional Review Board of New York Medical College.
References
1. Maghnie, M, Lindberg, A, Koltowska-Häggström, M, Ranke, MB. Magnetic resonance imaging of CNS in 15,043 children with GH deficiency in KIGS (pfizer international growth database). Eur J Endocrinol 2013;168:211–7. https://doi.org/10.1530/eje-12-0801.Search in Google Scholar PubMed
2. Teramoto, A, Hirakawa, K, Sanno, N, Osamura, Y. Incidental pituitary lesions in 1,000 unselected autopsy specimens. Radiology 1994;193:161–4. https://doi.org/10.1148/radiology.193.1.8090885.Search in Google Scholar PubMed
3. Elster, AD. Modern imaging of the pituitary. Radiology 1993;187:1–14. https://doi.org/10.1148/radiology.187.1.8451394.Search in Google Scholar PubMed
4. Hoang, JK, Hoffman, AR, González, RG, Wintermark, M, Glenn, B, Pandharipande, PV, et al.. Management of incidental pituitary findings on CT, MRI, and 18 F-fluorodeoxyglucose PET: a white paper of the ACR incidental findings committee. J Am Coll Radiol 2018;15:966–72. https://doi.org/10.1016/j.jacr.2018.03.037.Search in Google Scholar PubMed
5. Kessler, M, Tenner, M, Frey, M, Noto, R. Pituitary volume in children with growth hormone deficiency, idiopathic short stature and controls. J Pediatr Endocrinol Metab 2016;29:1195–200. https://doi.org/10.1515/jpem-2015-0404.Search in Google Scholar PubMed
6. Krasnow, N, Pogostin, B, Haigney, J, Groh, B, Weiler, W, Tenner, M, et al.. The prevalence and volumetry of pituitary cysts in children with growth hormone deficiency and idiopathic short stature. J Pediatr Endocrinol Metab 2018;31:1267–71.10.1515/jpem-2017-0437Search in Google Scholar PubMed
7. Kanter, AS, Sansur, CA, Jane, JA, Laws, ER. Rathke’s cleft cysts. Front Horm Res 2006;34:127–57.10.1159/000091579Search in Google Scholar PubMed
8. Zada, G, Ditty, B, McNatt, SA, McComb, JG, Krieger, MD. Surgical treatment of Rathke cleft cysts in children. Neurosurgery 2009;64:1132–7. https://doi.org/10.1227/01.neu.0000341873.20737.56.Search in Google Scholar PubMed
9. Kim, JE, Kim, JH, Kim, OL, Paek, SH, Kim, DG, Chi, JG, et al.. Surgical treatment of symptomatic Rathke cleft cysts: clinical features and results with special attention to recurrence. J Neurosurg 2004;100:33–40. https://doi.org/10.3171/jns.2004.100.1.0033.Search in Google Scholar PubMed
10. Aho, CJ, Liu, C, Zelman, V, Couldwell, WT, Weiss, MH. Surgical outcomes in 118 patients with Rathke cleft cysts. J Neurosurg 2005;102:189–93. https://doi.org/10.3171/jns.2005.102.2.0189.Search in Google Scholar PubMed
11. Trifanescu, R, Stavrinides, V, Plaha, P, Cudlip, S, Byrne, JV, Ansorge, O, et al.. Outcome in surgically treated Rathke’s cleft cysts: long-term monitoring needed. Eur J Endocrinol 2011;165:33–7. https://doi.org/10.1530/eje-11-0142.Search in Google Scholar
12. Jahangiri, A, Molinaro, AM, Tarapore, PE, Blevins, L, Auguste, KI, Gupta, N, et al.. Rathke cleft cysts in pediatric patients: presentation, surgical management, and postoperative outcomes. Neurosurg Focus 2011;31:E3. https://doi.org/10.3171/2011.5.focus1178.Search in Google Scholar PubMed
13. Eguchi, K, Uozumi, T, Arita, K, Kurisu, K, Yano, T, Sumida, M, et al.. Pituitary function in patients with Rathke’s cleft cyst: significance of surgical management. Endocr J 1994;41:535–40. https://doi.org/10.1507/endocrj.41.535.Search in Google Scholar PubMed
14. Potts, MB, Jahangiri, A, Lamborn, KR, Blevins, LS, Kunwar, S, Aghi, MK. Suprasellar Rathke cleft cysts: clinical presentation and treatment outcomes. Neurosurgery 2011;69:1058–68. https://doi.org/10.1227/neu.0b013e318228bcea.Search in Google Scholar PubMed
15. Nishioka, H, Haraoka, J, Izawa, H, Ikeda, Y. Headaches associated with Rathke’s cleft cyst. Headache 2006;46:1580–6. https://doi.org/10.1111/j.1526-4610.2006.00539.x.Search in Google Scholar PubMed
16. Marieb, EN, Wilhelm, PB, Mallatt, J. Human anatomy. Glenview, IL: Pearson Education, Inc.; 2014:526 p.Search in Google Scholar
17. Baird, K, McCroskey, J, Arynchyna, A, Abdullatif, H, Ashraf, AP, Simpson, L, et al.. Incidental pituitary cysts in children: does growth hormone treatment affect cyst size? Endocr Pract 2021;27:1128–32. https://doi.org/10.1016/j.eprac.2021.04.887.Search in Google Scholar PubMed
18. Sanno, N, Oyama, K, Tahara, S, Teramoto, A, Kato, Y. A survey of pituitary incidentaloma in Japan. Eur J Endocrinol 2003;149:123–7. https://doi.org/10.1530/eje.0.1490123.Search in Google Scholar PubMed
19. Culver, SA, Grober, Y, Ornan, DA, Patrie, JT, Oldfield, EH, Jane, JA, et al.. A case for conservative management: characterizing the natural history of radiographically diagnosed rathke cleft cysts. J Clin Endocrinol Metab 2015;100:3943–8. https://doi.org/10.1210/jc.2015-2604.Search in Google Scholar PubMed PubMed Central
20. Wong, AP, Pipitone, J, Park, MT, Dickie, EW, Leonard, G, Perron, M, et al.. Estimating volumes of the pituitary gland from T1-weighted magnetic-resonance images: effects of age, puberty, testosterone, and estradiol. Neuroimage 2014;94:216–21. https://doi.org/10.1016/j.neuroimage.2014.02.030.Search in Google Scholar PubMed
21. Sharafuddin, MJ, Luisiri, A, Garibaldi, LR, Fulk, DL, Klein, JB, Gillespie, KN, et al.. MR imaging diagnosis of central precocious puberty: importance of changes in the shape and size of the pituitary gland. AJR Am J Roentgenol 1994;162:1167–73. https://doi.org/10.2214/ajr.162.5.8166005.Search in Google Scholar PubMed
22. Takano, K, Utsunomiya, H, Ono, H, Ohfu, M, Okazaki, M. Normal development of the pituitary gland: assessment with three-dimensional MR volumetry. Am J Neuroradiol 1999;20:312–5.Search in Google Scholar
23. Han, SJ, Rolston, JD, Jahangiri, A, Aghi, MK. Rathke’s cleft cysts: review of natural history and surgical outcomes. J Neuro Oncol 2013;117:197–203. https://doi.org/10.1007/s11060-013-1272-6.Search in Google Scholar PubMed
© 2022 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Editorial
- Disorders of sex development – biologic, genetic, cultural, societal, and psychologic diversity of the human nature
- Review
- Diagnostic approach in 46, XY DSD: an endocrine society of bengal (ESB) consensus statement
- Original Articles
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- Evaluation of bladder dysfunction in children and adolescents with type 1 diabetes mellitus by uroflowmetry
- All aspects of galactosemia: a single center experience
- The evolution of pituitary cysts in growth hormone-treated children
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- Case Reports
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- Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report
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Articles in the same Issue
- Frontmatter
- Editorial
- Disorders of sex development – biologic, genetic, cultural, societal, and psychologic diversity of the human nature
- Review
- Diagnostic approach in 46, XY DSD: an endocrine society of bengal (ESB) consensus statement
- Original Articles
- Penile diameter during puberty in boys: a retrospective analysis of longitudinally obtained data
- Evaluation of bladder dysfunction in children and adolescents with type 1 diabetes mellitus by uroflowmetry
- All aspects of galactosemia: a single center experience
- The evolution of pituitary cysts in growth hormone-treated children
- Phototherapy-induced hypocalcemia and hypoparathyroidism in icteric term newborns
- Clinical and laboratory evaluation of children with congenital hyperinsulinism: a single center experience
- Does cystatin C have an immunomodulatory role in Hashimoto’s thyroiditis?
- Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition
- Features of BSCL2 related congenital generalized lipodystrophy in China: long-term follow-up of three patients and literature review
- Case Reports
- Congenital adrenal hyperplasia with a CYP21A2 deletion overlapping the tenascin-X gene: an atypical presentation
- The smallest dislocated microduplication of Xq27.1 harboring SOX3 gene associated with XX male phenotype
- Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report
- Human chorionic gonadotrophin secreting adrenocortical neoplasm presenting with peripheral precocious puberty in an infant
- Atypical familial diabetes associated with a novel NEUROD1 nonsense variant