1H-MRS metabolic patterns for distinguishing between meningiomas and other brain tumors

https://doi.org/10.1016/S0730-725X(03)00097-3Get rights and content

Abstract

Yet meningiomas have characteristic neuroimaging features, some other lesions are still confusing with meningiomas. The aim of this study was trying to find the typical 1H-MRS metabolic factors of histologic subtyped meningiomas, schwannomas, metastases, and other brain tumors for differential diagnosis among them. 1H-MRS using STEAM (TE/30 ms, TR/2 sec) and PRESS (TE/288 ms, TR/2 sec) sequences were performed on 44 untreated brain tumors. Obtained metabolic patterns from the typical spectra of meningioma, schwannoma, metastasis were compared with each other or other brain tumors to evaluate the usefulness for diagnosis between them. Alanine(Ala) was observed in 15 cases of the 19 meningiomas with a little variation to three histologic subtypes, while minimal lipids were observed in every 19 meningiomas. Elevated glutamate/glutamine(Glx) was detected in 12 cases of the meniningiomas. Increased myo-inositol(mI) was detected in 11 cases of the 13 schwannomas. Dominant lipids signals as well as long-T2 lipids were detected in every metastasis in conjunction with elevated choline (Cho). Enhanced Glx was observed in 4 cases of the 8 metastases without correlation of primary tumor site or types. Hemangiopericytoma showed different spectral patterns from typical meningiomas: only dominant Cho, minimal lipids and absence of Ala or Glx signals. These metabolic patterns in typical tumors may provide a basis for differential diagnosis (average value of χ2 = 23.33, p < 0.01) between meningiomas and schwannomas as well as metastases. However proton spectral distinction among the different histologic subtypes of meningiomas was not definite.

Introduction

With advent of MRI, the quality of preoperative diagnostic imaging for meningiomas have been improved dramatically and most of cases it is not difficult to diagnose meningiomas with conventional MRI with gadolinium-DTPA enhancement. With current MR imaging technique, dural attachment, sinus involvement and even information about a histologic subtype, vascularity and tumor’s consistency are possible. [1] Yet meningiomas have characteristic neuroimaging features, some other lesions are still confusing with meningiomas. Especially it is not easy to distinguish menigiomas from hemagiopericytomas, schwannomas occurring at the cerebello-pontine angle, dural metastatic tumors mimicking meningiomas. Surgical procedures or therapeutic plan of each tumorous condition may be quite different depending on the preoperative impression. [2] When diagnosing atypical tumor or tumor-like transformation, and preoperative diagnosis is not confident just by using conventional MRI and even using contrast-enhanced MRI methods, it is frequently requested to rule out meningiomas unambiguously. In addition the more detailed identification of the subtype of meningiomas may provide valuable information prior to surgical planning.

Studies of extracts of surgical specimens have generally indicated an increase in Alanine in meningiomas and an increase in myo-inositol in schwannomas. [3], [4] Elevation of Glx were observed in the extracts of surgically excised samples of meningiomas [5] and in an in vivo study. [6] However these findings have been still controversial without extended in vivo studies with multiple cases of meningiomas or schwannomas. In vivo MRS studies of human metastasis show a similar correlation between metabolic features and histopathological grade. Lactate was more likely to be present in late stage than in early or intermediate stage metastasis. [7], [8] Lipid was recognized to occur in tumors of higher histopathological grade, [8] and was correlated with the amount of microscopic cellular necrosis. [7], [9] However at present MRS cannot reliably characterize histologic types or subtypes of tumors in the clinical routine as the metabolic patterns seen in in vivo MRS are not sufficiently correlating to histologic diagnosis.

In this study localized proton spectroscopy was investigated on the untreated tumors diagnosed as meningiomas, schwannomas, metastases and other brain lesions by only the MRI basis, which were substantially confirmed with biopsy. We evaluated the potential significance of MRS findings of new metabolic markers in the pre-operative differential diagnosis of these brain tumors. Spectral characteristics of meningiomas were investigated according to the histologic subtypes retrospectively.

Section snippets

Patients

Forty-five untreated brain tumors were examined by 1H MRS. Meningioma (N = 19), schwannomas (n = 13), metastases (n = 8), hemangiopericytoma (n = 3), osteosarcoma (n = 1) were included in the examined patients. Histologic types of tumor were confirmed by intraoperative biopsy after obtaining proton MR spectra.

MRI methods

Localizing imaging was obtained by T1-weighted (TR/TE:489/15, two NEX, matrix size 256 × 192) and T2-weighted images (TR/TE:3500/98 ms, one NEX, matrix 256 × 224) using spin echo and fast

Typical spectral patterns of meningioma

There was a marked reduction in NAA in every meningiomas, while marked reduction of Cr occurred in only 50% cases of the examined menimgiomas. Observed 1H NMR spectral patterns were described in Fig. 1, Fig. 2, and summarized in Table 1. Relative peak height ratio [Cr/Cho] was estimated. Detection of some amino acids resonances, such as elevated Glx or Ala, was most notable. Ala resonance was detected at 1.55 ppm in 15 cases of all 19 patients. In addition elevated Glx resonances were

Meningiomas vs. schwannomas

Previous studies of other laboratories reported a marked reduction of both the N-acetylaspartate (NAA) and phosphocreatine (PCr)/creatine (Cr) peaks in meningioma [14]. It was reported that this reduction was greater than that seen in astrocytoma. Reduction in or absence of NAA expressed the absence of neurons and axons from most tumors, which are histologically derived from astrocytes, which entirely lack NAA (glioma), connective tissue (meningiomas), or from remote tissues of nonneuronal

Conclusions

Alternative or simultaneous observations of Ala, elevated Glx, minimal lipids and the resonance at 3.8 ppm in meningiomas appeared to be potential metabolic factors for discriminating other brain tumors. Enhanced mI in schwannomas and long-T2 lipids of metastases may provide another information for the differential diagnosis from others. Enhanced Glx observed in a couple of metastases was not correlated to primary tumor types or tumor site. However it remains to be elucidated with further

References (28)

  • P.E. Sijens et al.

    1H NMR spectroscopy detection of lipids and lactate in metastatic brain tumors

    NMR in Biomed

    (1996)
  • T. Kimura et al.

    In Vivo single-voxel proton MR spectroscopy in brain lesions with ring-like enhancement

    NMR in Biomed

    (2001)
  • P.A. Bottomley

    Spatial Localization in NMR spectroscopy in vivo

    Ann NY Acad Sci

    (1987)
  • E.R. Danielsen et al.
  • Cited by (0)

    View full text