Skip to main content
Top
Published in: Acta Neurochirurgica 11/2021

01-11-2021 | Magnetic Resonance Imaging | Original Article - Brain Tumors

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

Authors: Ai Muroi, Shingo Takano, Takao Tsurubuchi, Tomokazu Sekine, Hiroko Fukushima, Ryoko Suzuki, Yuni Yamaki, Masahide Matsuda, Hiroyoshi Akutsu, Eiichi Ishikawa

Published in: Acta Neurochirurgica | Issue 11/2021

Login to get access

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.
Literature
1.
go back to reference 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 76:27–36CrossRef 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 76:27–36CrossRef
2.
go back to reference Chaudhry NS, Ahmad FU, Whittington E, Schatz N, Morcos JJ (2015) Primary intrinsic chiasmal germinoma. J Neuroophthalmol 35:171–174CrossRef Chaudhry NS, Ahmad FU, Whittington E, Schatz N, Morcos JJ (2015) Primary intrinsic chiasmal germinoma. J Neuroophthalmol 35:171–174CrossRef
3.
go back to reference 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 95:437–443CrossRef 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 95:437–443CrossRef
4.
go back to reference 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) 12:2621–2626CrossRef 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) 12:2621–2626CrossRef
5.
go back to reference 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 96:235–243CrossRef 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 96:235–243CrossRef
6.
go back to reference 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–e26546CrossRef 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–e26546CrossRef
7.
go back to reference 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 36:2047–2054CrossRef 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 36:2047–2054CrossRef
8.
go back to reference 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 57:23–31CrossRef 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 57:23–31CrossRef
9.
go back to reference 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 86:446–455CrossRef 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 86:446–455CrossRef
10.
go back to reference 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–S35CrossRef 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–S35CrossRef
11.
go back to reference Miller NR (2004) Primary tumours of the optic nerve and its sheath. Eye (Lond) 18:1026–1037CrossRef Miller NR (2004) Primary tumours of the optic nerve and its sheath. Eye (Lond) 18:1026–1037CrossRef
12.
go back to reference Molineus A, Boxberger N, Redlich A, Vorwerk P (2013) Time to diagnosis of brain tumors in children: a single-centre experience. Pediatr Int 55:305–309CrossRef Molineus A, Boxberger N, Redlich A, Vorwerk P (2013) Time to diagnosis of brain tumors in children: a single-centre experience. Pediatr Int 55:305–309CrossRef
13.
go back to reference Nadkarni TD, Fattepurkar SC, Desai KI, Goel A (2004) Intracranial optic nerve germinoma. J Clin Neurosci 11:559–561CrossRef Nadkarni TD, Fattepurkar SC, Desai KI, Goel A (2004) Intracranial optic nerve germinoma. J Clin Neurosci 11:559–561CrossRef
14.
go back to reference 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 143:1–8CrossRef 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 143:1–8CrossRef
15.
go back to reference 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 29:1871–1881CrossRef 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 29:1871–1881CrossRef
16.
go back to reference 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 61:7268–7276PubMed 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 61:7268–7276PubMed
17.
go back to reference Sethi RV, Marino R, Niemierko A, Tarbell NJ, Yock TI, MacDonald SM (2013) Delayed diagnosis in children with intracranial germ cell tumors. J Pediatr 163:1448–1453CrossRef Sethi RV, Marino R, Niemierko A, Tarbell NJ, Yock TI, MacDonald SM (2013) Delayed diagnosis in children with intracranial germ cell tumors. J Pediatr 163:1448–1453CrossRef
18.
go back to reference 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 28:93–100CrossRef 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 28:93–100CrossRef
19.
go back to reference 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 33:1–8CrossRef 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 33:1–8CrossRef
21.
go back to reference 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 84:846–854CrossRef 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 84:846–854CrossRef
22.
go back to reference Xia C, Liu Z, Zhang R, Mao Y, Wang Y (2011) Primary intrinsic optic chiasm germinoma. J Clin Neurosci 18:860–862CrossRef Xia C, Liu Z, Zhang R, Mao Y, Wang Y (2011) Primary intrinsic optic chiasm germinoma. J Clin Neurosci 18:860–862CrossRef
23.
go back to reference 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–e479CrossRef 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–e479CrossRef
24.
go back to reference (2017) Brain tumor registry of Japan (2005–2008). Neurol Med Chir (Tokyo) 57:9–102 (2017) Brain tumor registry of Japan (2005–2008). Neurol Med Chir (Tokyo) 57:9–102
25.
go back to reference (2009) Report of brain tumor registry of Japan (1984–2000) Neurol Med Chir (Tokyo) 49 Suppl:PS1–96 (2009) Report of brain tumor registry of Japan (1984–2000) Neurol Med Chir (Tokyo) 49 Suppl:PS1–96
Metadata
Title
Involvement of the optic pathway and outcome of visual function in patients with neurohypophyseal germ cell tumor
Authors
Ai Muroi
Shingo Takano
Takao Tsurubuchi
Tomokazu Sekine
Hiroko Fukushima
Ryoko Suzuki
Yuni Yamaki
Masahide Matsuda
Hiroyoshi Akutsu
Eiichi Ishikawa
Publication date
01-11-2021
Publisher
Springer Vienna
Published in
Acta Neurochirurgica / Issue 11/2021
Print ISSN: 0001-6268
Electronic ISSN: 0942-0940
DOI
https://doi.org/10.1007/s00701-021-04946-5

Other articles of this Issue 11/2021

Acta Neurochirurgica 11/2021 Go to the issue

Letter to the Editor (by Invitation) - Spine degenerative

Reply to the Letter: Failed back surgery syndrome, a term overdue for replacement