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Combined use of 18 F-FDG PET and corticosteroid for diagnosis of deep-seated primary central nervous system lymphoma without histopathological confirmation

  • Clinical Article - Brain Tumors
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Abstract

Background

Although histological diagnosis is indispensable in treating primary central nervous system lymphoma (PCNSL), we sometimes face an intractable situation in which tissue can be obtained only from a deep-seated brain lesion. In place of a histological diagnosis, the diagnostic adequacy of the combined use of 18 F-FDG PET and corticosteroid administration for PCNSL located in a deep-seated brain structure is reported.

Methods

Patients with a deep-seated tumor were treated as having PCNSL without histological confirmation, based on the following criteria: (1) there was no evidence of systemic malignancy; (2) the tumor showed an extremely high FDG uptake relative to normal gray matter on pretreatment 18 F-FDG PET; (3) the tumor decreased in size 1 week after diagnostic therapy by corticosteroid administration on contrast-enhanced T1-weighted magnetic resonance imaging (MRI). FDG uptake of the lesion was evaluated by the maximum of standardized uptake values (SUVmax) and tumor-to-normal ratio of the SUV (T/N ratio). The extent of the tumor reduction was calculated by volumetric analysis for the treatment response to corticosteroid administration.

Results

Ten patients (4 males and 6 females) matched these criteria. On pretreatment 18 F-FDG PET, mean SUVmax in the tumor was 24.8 (8.75–60.75), and mean T/N ratio was 3.24 (2.17–5.12). The extent of tumor volume reduction was shown to be 21 to 68 % 1 week after diagnostic therapy by corticosteroids. Mean total dose and duration of corticosteroids were 719 mg as prednisolone and 6.5 days, respectively. Nine patients achieved complete response and one patient achieved partial response on MRI after standard treatment for PCNSL with high-dose methotrexate and/or whole-brain irradiation.

Conclusion

Although the value of biopsy is universal, combining 18 F-FDG PET and corticosteroid administration is an important alternative method that may lead to the diagnosis of deep-seated PCNSLs in cases with intractable histopathological confirmations.

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References

  1. Andersen C, Haselgrove JC, Doenstrup S, Astrup J, Gyldensted C (1993) Resorption of peritumoural oedema in cerebral gliomas during dexamethasone treatment evaluated by NMR relaxation time imaging. Acta Neurochir (Wien) 122:218–224

    Article  CAS  Google Scholar 

  2. Baraniskin A, Deckert M, Schulte-Altedorneburg G, Schlegel U, Schroers R (2011) Current strategies in the diagnosis of diffuse large B-cell lymphoma of the central nervous system. Br J Haematol 156:421–432

    Article  PubMed  Google Scholar 

  3. Bolat S, Berding G, Dengler R, Stangel M, Trebst C (2009) Fluorodeoxyglucose positron emission tomography (FDG-PET) is useful in the diagnosis of neurosarcoidosis. J Neurol Sci 287:257–259

    Article  CAS  PubMed  Google Scholar 

  4. Bromberg JE, Siemers MD, Taphoorn MJ (2002) Is a “vanishing tumor” always a lymphoma. Neurology 59:762–764

    Article  CAS  PubMed  Google Scholar 

  5. Hall WA (1998) The safety and efficacy of stereotactic biopsy for intracranial lesions. Cancer 82:1749–1755

    Article  CAS  PubMed  Google Scholar 

  6. Karantanis D, O’Eill BP, Subramaniam RM, Witte RJ, Mullan BP, Nathan MA, Lowe VJ, Peller PJ, Wiseman GA (2007) 18F-FDG PET/CT in primary central nervous system lymphoma in HIV-negative patients. Nucl Med Commun 28:834–841

    Article  PubMed  Google Scholar 

  7. Kongkham PN, Knifed E, Tamber MS, Bernstein M (2008) Complications in 622 cases of frame-based stereotactic biopsy, a decreasing procedure. Can J Neurol Sci 35:79–84

    Article  PubMed  Google Scholar 

  8. Kuker W, Nagele T, Korfel A, Heckl S, Thiel E, Bamberg M, Weller M, Herrlinger U (2005) Primary central nervous system lymphomas (PCNSL): MRI features at presentation in 100 patients. J Neurooncol 72:169–177

    Article  PubMed  Google Scholar 

  9. Makino K, Hirai T, Nakamura H, Murakami R, Kitajima M, Shigematsu Y, Nakashima R, Shiraishi S, Uetani H, Iwashita K, Akter M, Yamashita Y, Kuratsu J (2011) Does adding FDG-PET to MRI improve the differentiation between primary cerebral lymphoma and glioblastoma? Observer performance study. Ann Nucl Med 25:432–438

    Article  PubMed  Google Scholar 

  10. Mathew BS, Carson KA, Grossman SA (2006) Initial response to glucocorticoids. Cancer 106:383–387

    Article  PubMed  Google Scholar 

  11. Mohile NA, Deangelis LM, Abrey LE (2008) Utility of brain FDG-PET in primary CNS lymphoma. Clin Adv Hematol Oncol 6(818–820):840

    Google Scholar 

  12. Ng D, Jacobs M, Mantil J (2006) Combined C-11 methionine and F-18 FDG PET imaging in a case of neurosarcoidosis. Clin Nucl Med 31:373–375

    Article  PubMed  Google Scholar 

  13. Omuro AM, Leite CC, Mokhtari K, Delattre JY (2006) Pitfalls in the diagnosis of brain tumours. Lancet Neurol 5:937–948

    Article  PubMed  Google Scholar 

  14. Reni M, Ferreri AJ, Garancini MP, Villa E (1997) Therapeutic management of primary central nervous system lymphoma in immunocompetent patients: results of a critical review of the literature. Ann Oncol 8:227–234

    Article  CAS  PubMed  Google Scholar 

  15. Roelcke U, Leenders KL (1999) Positron emission tomography in patients with primary CNS lymphomas. J Neurooncol 43:231–236

    Article  CAS  PubMed  Google Scholar 

  16. Rosenfeld SS, Hoffman JM, Coleman RE, Glantz MJ, Hanson MW, Schold SC (1992) Studies of primary central nervous system lymphoma with fluorine-18-fluorodeoxyglucose positron emission tomography. J Nucl Med 33:532–536

    CAS  PubMed  Google Scholar 

  17. Spaepen K, Stroobants S, Verhoef G, Mortelmans L (2003) Positron emission tomography with [(18)F]FDG for therapy response monitoring in lymphoma patients. Eur J Nucl Med Mol Imaging 30(Suppl 1):S97–105

    Article  PubMed  Google Scholar 

  18. Yamaguchi S, Hirata K, Kobayashi H, Shiga T, Manabe O, Kobayashi K, Motegi H, Terasaka S, Houkin K (2014) The diagnostic role of (18)F-FDG PET for primary central nervous system lymphoma. Ann Nucl Med 28:603–609

    Article  CAS  PubMed  Google Scholar 

  19. Zacharia TT, Law M, Naidich TP, Leeds NE (2008) Central nervous system lymphoma characterization by diffusion-weighted imaging and MR spectroscopy. J Neuroimaging 18:411–417

    Article  PubMed  Google Scholar 

  20. Zaki HS, Jenkinson MD, Du Plessis DG, Smith T, Rainov NG (2004) Vanishing contrast enhancement in malignant glioma after corticosteroid treatment. Acta Neurochir (Wien) 146:841–845

    Article  CAS  Google Scholar 

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Correspondence to Shunsuke Terasaka.

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Yamaguchi, S., Hirata, K., Kaneko, S. et al. Combined use of 18 F-FDG PET and corticosteroid for diagnosis of deep-seated primary central nervous system lymphoma without histopathological confirmation. Acta Neurochir 157, 187–194 (2015). https://doi.org/10.1007/s00701-014-2290-7

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  • DOI: https://doi.org/10.1007/s00701-014-2290-7

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