Skip to main content

Advertisement

Log in

Involvement of the optic pathway and outcome of visual function in patients with neurohypophyseal germ cell tumor

  • Original Article - Brain Tumors
  • Published:
Acta Neurochirurgica Aims and scope Submit manuscript

Abstract

Background

Patients with neurohypophyseal germ cell tumors (GCTs) typically present with visual problems. Hence, this study aimed to assess optic pathway involvement based on clinical and radiological findings and to validate the outcome of visual function.

Methods

A total of 16 patients with newly diagnosed neurohypophyseal GCTs who were treated at the University of Tsukuba Hospital between 2000 and 2020 were included in this study.

Results

The median interval from symptom onset to diagnosis was 173.5 days (range, 33–1588 days). Patients with visual disturbance at diagnosis had a longer time to diagnosis compared with those without. Ophthalmologic abnormalities were frequently observed, with an incidence rate of 69%. Fifty percent of patients exhibited optic pathway involvement detected via magnetic resonance imaging (MRI). Visual impairment was more severe in the patients with optic pathway involvement (p = 0.002). Post-treatment visual impairment was improved but was still significantly severe in patients with optic pathway involvement than in those without involvement (p = 0.010). Visual field deficit more likely remained with an improvement rate of 50%, whereas the improvement rate of visual acuity was 78%. Further, none developed late-onset visual deterioration during the follow-up period.

Conclusions

Visual disturbance and optic pathway involvement are common in neurohypophyseal GCTs. Visual impairment particularly in patients with optic pathway involvement on MRI is more likely to remain at follow-up, although the outcome of visual function is acceptable in most cases.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

Deidentified raw data is available upon request.

Code availability

Available upon request.

References

  1. Azizi AA, Heßler K, Leiss U, Grylli C, Chocholous M, Peyrl A, Gojo J, Slavc I (2017) From symptom to diagnosis—the prediagnostic symptomatic interval of pediatric central nervous system tumors in Austria. Pediatr Neurol 76:27–36

    Article  Google Scholar 

  2. Chaudhry NS, Ahmad FU, Whittington E, Schatz N, Morcos JJ (2015) Primary intrinsic chiasmal germinoma. J Neuroophthalmol 35:171–174

    Article  Google Scholar 

  3. DiLuna ML, Two AM, Levy GH, Patel T, Huttner AJ, Duncan CC, Piepmeier JM (2009) Primary, non-exophytic, optic nerve germ cell tumors. J Neurooncol 95:437–443

    Article  Google Scholar 

  4. Esfahani DR, Alden T, DiPatri A, Xi G, Goldman S, Tomita T (2020) Pediatric suprasellar germ cell tumors: a clinical and radiographic review of solitary vs. bifocal tumors and its therapeutic implications. Cancers (Basel) 12:2621–2626

    Article  CAS  Google Scholar 

  5. Fahlbusch R (2002) Schott W (2002) Pterional surgery of meningiomas of the tuberculum sellae and planum sphenoidale: surgical results with special consideration of ophthalmological and endocrinological outcomes. J Neurosurg 96:235–243

    Article  Google Scholar 

  6. Frappaz D, Pedone C, Thiesse P, Szathmari A, Conter CF, Mottolese C, Carrie C (2017) Visual complaints in intracranial germinomas. Pediatr Blood Cancer 64:e26543–e26546

    Article  Google Scholar 

  7. Hirata K, Muroi A, Tsurubuchi T, Fukushima H, Suzuki R, Yamaki Y, Ishikawa E, Matsumura A (2020) Time to diagnosis and clinical characteristics in pediatric brain tumor patients. Childs Nerv Syst 36:2047–2054

    Article  Google Scholar 

  8. Ho R-W, Huang H-M, Ho J-T (2015) The influence of pituitary adenoma size on vision and visual outcomes after trans-sphenoidal adenectomy: a report of 78 cases. J Korean Neurosurg Soc 57:23–31

    Article  CAS  Google Scholar 

  9. Matsutani M, Sano K, Takakura K, Fujimaki T, Nakamura O, Funata N, Seto T (1997) Primary intracranial germ cell tumors: a clinical analysis of 153 histologically verified cases. J Neurosurg 86:446–455

    Article  CAS  Google Scholar 

  10. Mayo C, Martel MK, Marks LB, Flickinger J, Nam J, Kirkpatrick J (2010) Radiation dose-volume effects of optic nerves and chiasm. Int J Radiat Oncol Biol Phys 76:S28–S35

    Article  Google Scholar 

  11. Miller NR (2004) Primary tumours of the optic nerve and its sheath. Eye (Lond) 18:1026–1037

    Article  CAS  Google Scholar 

  12. Molineus A, Boxberger N, Redlich A, Vorwerk P (2013) Time to diagnosis of brain tumors in children: a single-centre experience. Pediatr Int 55:305–309

    Article  Google Scholar 

  13. Nadkarni TD, Fattepurkar SC, Desai KI, Goel A (2004) Intracranial optic nerve germinoma. J Clin Neurosci 11:559–561

    Article  Google Scholar 

  14. Patel V, McNinch NL, Rush S (2019) Diagnostic delay and morbidity of central nervous system tumors in children and young adults: a pediatric hospital experience. J Neurooncol 143:1–8

    Article  Google Scholar 

  15. Phi JH, Kim S-K, Lee YA, Shin CH, Cheon J-E, Kim I-O, Yang SW, Wang K-C (2013) Latency of intracranial germ cell tumors and diagnosis delay. Childs Nerv Syst 29:1871–1881

    Article  Google Scholar 

  16. Schneider DT, Schuster AE, Fritsch MK, Hu J, Olson T, Lauer S, Göbel U, Perlman EJ (2001) Multipoint imprinting analysis indicates a common precursor cell for gonadal and nongonadal pediatric germ cell tumors. Cancer Res 61:7268–7276

    PubMed  CAS  Google Scholar 

  17. Sethi RV, Marino R, Niemierko A, Tarbell NJ, Yock TI, MacDonald SM (2013) Delayed diagnosis in children with intracranial germ cell tumors. J Pediatr 163:1448–1453

    Article  Google Scholar 

  18. Shay V, Fattal-Valevski A, Beni-Adani L, Constantini S (2011) Diagnostic delay of pediatric brain tumors in Israel: a retrospective risk factor analysis. Childs Nerv Syst 28:93–100

    Article  Google Scholar 

  19. Stocco C, Pilotto C, Passone E, Nocerino A, Tosolini R, Pusiol A, Cogo P (2017) Presentation and symptom interval in children with central nervous system tumors A single-center experience. Childs Nerv Syst 33:1–8

    Article  Google Scholar 

  20. Takami H, Graffeo CS, Perry A, Giannini C, Daniels DJ (2020) Epidemiology, natural history, and optimal management of neurohypophyseal germ cell tumors. J Neurosurg. https://doi.org/10.3171/2019.10.JNS191136

    Article  PubMed  Google Scholar 

  21. Takano S, Yamamoto T, Ishikawa E et al (2015) Improvement of long-term results with neoadjuvant chemotherapy and radiotherapy for central nervous system germinoma. World Neurosurg 84:846–854

    Article  Google Scholar 

  22. Xia C, Liu Z, Zhang R, Mao Y, Wang Y (2011) Primary intrinsic optic chiasm germinoma. J Clin Neurosci 18:860–862

    Article  Google Scholar 

  23. Zhang Y, Deng K, Zhu H, Lu L, Pan H, Ma W, Wang R, Yao Y (2019) Delays in diagnosis of pediatric histologically confirmed sellar germ cell tumors in china: a retrospective risk factor analysis. World Neurosurg 122:e472–e479

    Article  Google Scholar 

  24. (2017) Brain tumor registry of Japan (2005–2008). Neurol Med Chir (Tokyo) 57:9–102

  25. (2009) Report of brain tumor registry of Japan (1984–2000) Neurol Med Chir (Tokyo) 49 Suppl:PS1–96

Download references

Acknowledgements

We would like to thank Enago for their English language editing service.

Author information

Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. Material preparation and data collection were performed by Ai Muroi, Takao Tsurubuchi, Tomokazu Sekine, Hiroko Fukushima, Ryoko Suzuki, Yuni Yamaki, Masahide Matsuda, and Hiroyoshi Akutsu. The first draft of the manuscript was written by Ai Muroi, and all the authors commented on previous versions of the manuscript. Shingo Takano and Eiichi Ishikawa critically supervised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ai Muroi.

Ethics declarations

Ethics approval

This study was performed in accordance with the principles of the Declaration of Helsinki, and it was approved by the ethics committee of the University of Tsukuba Hospital (R02-202).

Consent to participate and publish

In accordance with the ethical standards of our institutional review board, a written informed consent was not required for retrospective analyses because this observational study did not modify existing diagnostic or therapeutic strategies. However, consent was obtained in the opt-out form on the website.

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

This article is part of the Topical Collection on Brain Tumors

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Muroi, A., Takano, S., Tsurubuchi, T. et al. Involvement of the optic pathway and outcome of visual function in patients with neurohypophyseal germ cell tumor. Acta Neurochir 163, 3191–3199 (2021). https://doi.org/10.1007/s00701-021-04946-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00701-021-04946-5

Keywords

Navigation