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Proton MR Spectroscopy of Central Neurocytoma Using Short and Long Echo Time

Rationale and Objectives

Central neurocytomas (CNCs) are rare benign tumors typically located in the lateral ventricle of the central nervous system. The authors report five patients with CNCs and review 16 previously published studies that included 52 patients with CNCs to explore the magnetic resonance spectroscopic features of CNCs.

Materials and Methods

Five patients with CNCs were retrospectively reviewed. They were examined using point-resolved spectroscopic series with short and/or long echo times. The integrals of choline, creatine, and the 3.55-ppm peak were determined using Magnetic Resonance User Interface software, and the metabolite ratios relative to creatine were obtained. In two cases, T2 relaxation times of choline and the metabolite resonance at 3.55 ppm were calculated using data points acquired with different echo times and an exponential decay model.

Results

Consistent with previously published studies, all five patients showed highly increased choline and reduced N-acetylaspartate and creatine. Four patients in the present study and 35 in published data demonstrated prominent peaks at 3.55 ppm, which were assigned to glycine because of its relaxation pattern and long T2 relaxation time. In addition, increased in vivo glutamate and glutamine was also confirmed in three patients examined with short echo times. Alanine and lactate peaks were observed in three and two patients, respectively.

Conclusions

The present study shows that the 3.55-ppm peak characteristic of CNC should be assigned to glycine according to its T2 relaxation time. Besides increased glycine and choline, the presence of glutamate or glutamine, which appears on series with short echo times, may further confirm the diagnosis of CNC.

Central neurocytoma (CNC) is a rare brain tumor of neuronal origin first identified by Hassoun et al in 1982, accounting for approximately .25% to .5% of all tumors in the central nervous system . It usually affects young adults aged 20 to 40 years . On conventional magnetic resonance imaging, CNC typically exhibits an intraventricular mass with hypointensity on T1-weighted images and hyperintensity on T2-weighted images, with mild to remarkable heterogeneous enhancement after the administration of gadolinium diethylenetriamine penta-acetic acid . However, it may be difficult to differentiate CNC from other intraventricular tumors on the basis of magnetic resonance imaging alone.

In vivo proton magnetic resonance spectroscopy (MRS) has been proven useful in providing biochemical information on these lesions. The spectroscopy of CNC is characterized by prominent choline (Cho) peak, small N-acetylaspartate (NAA) and creatine (Cr) peaks, and a 3.55-ppm peak, with or without alanine (Ala) or lactate (Lac). The 3.55-ppm peak is considered the biomarker of CNC, but whether it is glycine (Gly) or myoinositol (MI) has not been fully clarified. Also, most previous studies were performed at 1.5 T with long echo times (TEs). As a result, spectral resolution was relatively poor compared with that obtained at 3.0 T, and metabolites with short T2 relaxation times, such as glutamate and glutamine (Glx) may therefore be underestimated. In the present study, we report five patients with CNC, two of whom were examined using a 3.0-T scanner and three using both short and long TEs. We also review published MRS reports of CNC to outline its features on the basis of a larger case population.

Materials and methods

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Table 1

Patient Information of the Present Study

Patient Gender Age (y) Clinical Conditions Tumor Location MRI Findings Proliferation Index 1 F 24 Headache and vomiting Right LV T1↓, T2↑, hetero, cyst(+), Ca(+), he(+) >2% 2 M 35 Headache and vomiting Right LV T1↓, T2↑, hetero, cyst(+), Ca(+), he(+) 3%–7% 3 F 17 Headache, vomiting, and blurred vision Left LV T1↓, T2↑, cyst(+), Ca(+), he(−) <1% 4 F 31 Headache and vomiting Right LV Slightly T1↓, slightly T2↑, hetero, cyst(+), Ca(+), he(−) <1% 5 M 29 Headache and vomiting Left LV Slightly T1↓, slightly T2↑, hetero, cyst(+), Ca(+), he(−) <1%

Ca(+), with calcification; cyst(+), with cystic lesion; he(+), with hemorrhage; he(−), without hemorrhage; hetero, heterogeneous enhancement; LV, lateral ventricle; MRI, magnetic resonance imaging; ↓, hypointense; ↑, hyperintense.

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Ms=M0×exp(−2τT2), M

s

=

M

0

×

exp

(

2

τ

T

2

)

,

where M s denotes the signal intensity of the measurement at a given TE, M 0 denotes the signal intensity at a TE of 0 ms, and τ denotes TE/2.

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Results

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Figure 1, A 35-year-old man with central neurocytoma The lesion appears hypointense on a T1-weighted image (a) and hyperintense on a T2-weighted image (b) . Administration of gadolinium diethylenetriamine penta-acetic acid resulted in heterogeneous enhancement (c) . Magnetic resonance spectroscopy of the lesion at echo times (TEs) of 30 ms (d) and 135 ms (e) showed a higher choline peak and smaller N-acetylaspartate (NAA) and creatine peaks compared to peripheral normal brain (f) . Note that the 3.55-ppm singlet peak (long black arrow) did not attenuate dramatically when the TE was lengthened from 30 ms (d) to 135 ms (e) . A robust glutamate and glutamine peak (short black arrow) next to NAA can also be observed. Partially overlapped alanine (short open arrow) and lactate (long open arrow) were seen at 1.33 to 1.47 ppm, demonstrating phase reversal at a TE of 135 ms.

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Table 2

MRS Findings of CNCs in the Present Study and Published Data

Study Number of Patients Field Strength (T) TE (ms) MRS Findings NAA Cr Cho Average Cho/Cr 3.55-ppm Peak at Short TE 3.55-ppm Peak at Long TE Glx Ala Lac Present study Patient 1 3.0 30/135/270 ↓ ↓ ↑ 10.01 Yes Yes Yes Yes No Patient 2 3.0 30/135 ↓ ↓ ↑ 9.62 Yes Yes Yes Yes Yes Patient 3 1.5 68/136/272 ↓ ↓ ↑ 5.82 Yes Yes No No No Patient 4 1.5 30 ↓ ↓ ↑ 12.74 No NA Yes Yes Yes Patient 5 1.5 135 ↓ ↓ ↑ 5.15 NA Yes No No No Subtotal 5 ↓ (5/5) ↓ (5/5) ↑ (5/5) 8.67 3/4 4/4 3/5 3/5 2/5 Previous studies Shah et al 11 1.5 135 ↓ (8/11) ↓ (8/11) ↑ (11/11) NA NA 10/11 0/11 7/11 1/11 Bobek-Billewicz et al 2 3.0/1.5 135/144 ↓ (2/2) ↓ (2/2) ↑ (2/2) 3.84 NA 2/2 0/2 0/2 0/2 Majos et al 2 1.5 30/136 ↓ (2/2) ↓ (2/2) ↑ (2/2) NA 2/2 2/2 2/2 2/2 0/2 Kocaoglu et al 7 1.5 136 ↓ (7/7) ↓ (7/7) ↑ (7/7) 5.18 NA 1/7 0/7 0/7 1/7 Balaji et al 1 1.5 144 ↓ (1/1) ↓ (1/1) ↑ (1/1) NA NA 1/1 0/1 1/1 1/1 Yeh et al 3 1.5 35/144 ↓ (3/3) ↓ (3/3) ↑ (3/3) NA 2/2 3/3 0/3 0/3 0/3 Ueda et al 5 1.5 35 ↓ (5/5) ↓ (5/5) ↑ (5/5) 3.94 3/5 N/A 0/5 0/5 2/5 Krishnamoorthy et al 3 1.5 135 ↓ (3/3) ↓ (3/3) ↑ (3/3) NA NA 3/3 0/3 3/3 1/3 Kawaguchi et al 2 1.5 272 ↓ (2/2) ↓ (2/2) ↑ (2/2) NA NA 1/2 0/2 0/2 1/2 Chuang et al 3 3.0 144 ↓ (3/3) ↓ (3/3) ↑ (3/3) 2.2 NA 1/3 0/3 1/3 0/3 Jayasundar et al 2 1.5 135 ↓ (2/2) ↓ (2/2) ↑ (2/2) NA NA 2/2 0/2 2/2 0/2 Moller-Hartmann et al 1 1.5 135 ↓ (1/1) ↓ (1/1) ↑ (1/1) 2.42 NA 0/1 0/1 0/1 0/1 Kanamori et al 3 1.5 272 ↓ (3/3) ↓ (3/3) ↑ (3/3) NA NA 1/3 0/3 0/3 0/3 Ando et al 1 1.5 270 ↓ (1/1) ↓ (1/1) ↑ (1/1) NA NA 0/1 0/1 0/1 1/1 Kim et al 5 1.5 135 ↓ (5/5) ↓ (5/5) ↑ (5/5) 5.25 NA 5/5 0/5 0/5 5/5 Warmuth-Metz et al 1 1.5 135 ↓ (1/1) ↓ (1/1) ↑ (1/1) NA NA 0/1 0/1 0/1 1/1 Subtotal 52 ↓ (52/52) ↓ (52/52) ↑ (52/52) 4.30 7/9 32/47 2/52 16/52 14/52 Total 57 ↓ (57/57) ↓ (57/57) ↑ (57/57) 5.08 10/13 36/51 5/57 19/57 16/57

Ala, alanine; Cho, choline; CNC, central neurocytoma; Cr, creatine; Glx, glutamate and glutamine; Lac, lactate; MRS, magnetic resonance spectroscopic; NA, not available; NAA, N-acetylaspartate; TE, echo time.

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Discussion

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Conclusions

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References

  • 1. Hassoun J., Gambarelli D., Grisoli F., et. al.: Central neurocytoma. An electron-microscopic study of two cases. Acta Neuropathol 1982; 56: pp. 151-156.

  • 2. Hassoun J., Soylemezoglu F., Gambarelli D., et. al.: Central neurocytoma: a synopsis of clinical and histological features. Brain Pathol 1993; 3: pp. 297-306.

  • 3. De Tommasi A., D’Urso P.I., De Tommasi C., et. al.: Central neurocytoma: two case reports and review of the literature. Neurosurg Rev 2006; 29: pp. 339-347.

  • 4. Zhang D., Wen L., Henning T.D., et. al.: Central neurocytoma: clinical, pathological and neuroradiological findings. Clin Radiol 2006; 61: pp. 348-357.

  • 5. Majos C., Aguilera C., Cos M., et. al.: In vivo proton magnetic resonance spectroscopy of intraventricular tumours of the brain. Eur Radiol 2009; 19: pp. 2049-2059.

  • 6. Kocaoglu M., Ors F., Bulakbasi N., et. al.: Central neurocytoma: proton MR spectroscopy and diffusion weighted MR imaging findings. Magn Reson Imaging 2009; 27: pp. 434-440.

  • 7. Balaji R., Ramachandran K.: Multivoxel 1H MR spectroscopic approach to the diagnosis of intraventricular central neurocytoma. A case report. Neuroradiol J 2009; 22: pp. 175-178.

  • 8. Yeh I.B., Xu M., Ng W.H., et. al.: Central neurocytoma: typical magnetic resonance spectroscopy findings and atypical ventricular dissemination. Magn Reson Imaging 2008; 26: pp. 59-64.

  • 9. Ueda F., Suzuki M., Matsui O., et. al.: Automated MR spectroscopy of intra- and extraventricular neurocytomas. Magn Reson Med Sci 2007; 6: pp. 75-81.

  • 10. Krishnamoorthy T., Radhakrishnan V.V., Thomas B., et. al.: Alanine peak in central neurocytomas on proton MR spectroscopy. Neuroradiology 2007; 49: pp. 551-554.

  • 11. Kawaguchi T., Kumabe T., Shimizu H., et. al.: 201Tl-SPECT and 1H-MRS study of benign lateral ventricle tumors: differential diagnosis of subependymoma. Neurosurg Rev 2005; 28: pp. 96-103.

  • 12. Chuang M.T., Lin W.C., Tsai H.Y., et. al.: 3-T proton magnetic resonance spectroscopy of central neurocytoma: 3 case reports and review of the literature. J Comput Assist Tomogr 2005; 29: pp. 683-688.

  • 13. Jayasundar R., Shah T., Vaishya S., et. al.: In vivo and in vitro MR spectroscopic profile of central neurocytomas. J Magn Reson Imaging 2003; 17: pp. 256-260.

  • 14. Moller-Hartmann W., Krings T., Brunn A., et. al.: Proton magnetic resonance spectroscopy of neurocytoma outside the ventricular region—case report and review of the literature. Neuroradiology 2002; 44: pp. 230-234.

  • 15. Kanamori M., Kumabe T., Shimizu H., et. al.: (201)Tl-SPECT, (1)H-MRS, and MIB-1 labeling index of central neurocytomas: three case reports. Acta Neurochir (Wien) 2002; 144: pp. 157-163.

  • 16. Ando K., Ishikura R., Morikawa T., et. al.: Central neurocytoma with craniospinal dissemination. Magn Reson Med Sci 2002; 1: pp. 179-182.

  • 17. Kim D.G., Choe W.J., Chang K.H., et. al.: In vivo proton magnetic resonance spectroscopy of central neurocytomas. Neurosurgery 2000; 46: pp. 329-333.

  • 18. Warmuth-Metz M., Klein R., Sorensen N., et. al.: Central neurocytoma of the fourth ventricle. Case report. J Neurosurg 1999; 91: pp. 506-509.

  • 19. Shah T., Jayasundar R., Singh V.P., et. al.: MRS characterization of central neurocytomas using glycine. NMR Biomed 2011; 24: pp. 1408-1413.

  • 20. Bobek-Billewicz B., Hebda A., Stasik-Pres G., et. al.: Measurement of glycine in a brain and brain tumors by means of 1H MRS. Folia Neuropathol 2010; 48: pp. 190-199.

  • 21. Isobe T., Matsumura A., Anno I., et. al.: Quantification of cerebral metabolites in glioma patients with proton MR spectroscopy using T2 relaxation time correction. Magn Reson Imaging 2002; 20: pp. 343-349.

  • 22. Stanley J.A.: In vivo magnetic resonance spectroscopy and its application to neuropsychiatric disorders. Can J Psychiatry 2002; 47: pp. 315-326.

  • 23. Zeng Q., Liu H., Zhang K., et. al.: Noninvasive evaluation of cerebral glioma grade by using multivoxel 3D proton MR spectroscopy. Magn Reson Imaging 2011; 29: pp. 25-31.

  • 24. Miller B.L., Chang L., Booth R., et. al.: In vivo 1H MRS choline: correlation with in vitro chemistry/histology. Life Sci 1996; 58: pp. 1929-1935.

  • 25. Gupta R.K., Cloughesy T.F., Sinha U., et. al.: Relationships between choline magnetic resonance spectroscopy, apparent diffusion coefficient and quantitative histopathology in human glioma. J Neurooncol 2000; 50: pp. 215-226.

  • 26. Ernst T., Hennig J.: Coupling effects in volume selective 1H spectroscopy of major brain metabolites. Magn Reson Med 1991; 21: pp. 82-96.

  • 27. Xin L., Gambarota G., Mlynarik V., et. al.: Proton T2 relaxation time of J-coupled cerebral metabolites in rat brain at 9.4 T. NMR Biomed 2008; 21: pp. 396-401.

  • 28. Frahm J., Bruhn H., Gyngell M.L., et. al.: Localized proton NMR spectroscopy in different regions of the human brain in vivo. Relaxation times and concentrations of cerebral metabolites. Magn Reson Med 1989; 11: pp. 47-63.

  • 29. Hattingen E., Lanfermann H., Quick J., et. al.: 1H MR spectroscopic imaging with short and long echo time to discriminate glycine in glial tumours. MAGMA 2009; 22: pp. 33-41.

  • 30. Righi V., Andronesi O.C., Mintzopoulos D., et. al.: High-resolution magic angle spinning magnetic resonance spectroscopy detects glycine as a biomarker in brain tumors. Int J Oncol 2010; 36: pp. 301-306.

  • 31. DeBerardinis R.J., Mancuso A., Daikhin E., et. al.: Beyond aerobic glycolysis: transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis. Proc Natl Acad Sci U S A 2007; 104: pp. 19345-19350.

  • 32. Fan G., Sun B., Wu Z., et. al.: In vivo single-voxel proton MR spectroscopy in the differentiation of high-grade gliomas and solitary metastases. Clin Radiol 2004; 59: pp. 77-85.

  • 33. Sontheimer H.: A role for glutamate in growth and invasion of primary brain tumors. J Neurochem 2008; 105: pp. 287-295.

  • 34. Di Costanzo A., Trojsi F., Tosetti M., et. al.: Proton MR spectroscopy of the brain at 3 T: an update. Eur Radiol 2007; 17: pp. 1651-1662.

  • 35. Newsholme P., Procopio J., Lima M.M., et. al.: Glutamine and glutamate—their central role in cell metabolism and function. Cell Biochem Funct 2003; 21: pp. 1-9.

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