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CNS Involvement in Non-CNS Tumors

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Abstract

This chapter describes the clinical neuroradiology of three broad areas of brain and intracranial involvement with systemic malignancy: metastases, lymphoproliferative disorders, and paraneoplastic syndromes. Intracranial metastases can be parenchymal, leptomeningeal, and dural. They most commonly arise from breast, lung, and colon cancer and melanoma. The lymphoproliferative disorders concern a range of parenchymal and meningeal disorders in hematological cancer, namely, leukemia, systemic lymphoma, and posttransplant lymphoproliferative disorder. Primary CNS lymphoma is outside the scope of this chapter and discussed elsewhere in this book. The paraneoplastic syndromes have as a common denominator an immune-mediated response to a primary malignancy remote from the CNS. Paraneoplastic syndromes of the brain include autoimmune (limbic) encephalitis (also known as limbic encephalitis), paraneoplastic rhombencephalitis, and cerebellar degeneration.

While in many cases a primary malignancy is known, the CNS findings may be the presenting symptom. Prompt and accurate radiological diagnosis is of utmost importance in these cases for a timely systemic assessment and start of anticancer treatment. An important consideration is that tissue diagnosis is severely hampered by corticosteroid use in patients with lymphoma, which should therefore be withheld in any suspicion of lymphoma to avoid misdiagnosis and delayed treatment of these patients.

Differential diagnosis of CNS involvement with systemic disease is not always straightforward and may include primary brain tumors, but may also be complicated by coexisting morbidity (such as immunodeficiency in hematological cancer) or treatment effects (such as neurotoxicity of chemo- and radiation therapy). Advanced radiological techniques, such as MR perfusion imaging, MR spectroscopy, and PET imaging, may be helpful in selected cases.

This publication is endorsed by: European Society of Neuroradiology (www.esnr.org).

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Abbreviations

1.5T/3.0T:

1.5 Tesla/3.0 Tesla

2D/3D:

2 dimensional/3 dimensional

ADC:

Apparent diffusion coefficient

ADEM:

Acute disseminated encephalomyelitis

ALL:

Acute lymphoid leukemia

AML:

Acute myeloid leukemia

AMPA:

Alpha-amino-3-hydroxy-5-methyl-4-iso-xazolepropionic acid

Caspr2:

Contactin-associated protein-2

CBV:

Cerebral blood volume

Cho:

Choline

CNS:

Central nervous system

Cr:

Creatine

CSF:

Cerebrospinal fluid

CT:

Computed tomography

DCE:

Dynamic contrast enhanced

DNER:

Delta/notch-like epidermal growth factor -related receptor

DSC:

Dynamic susceptibility contrast

DWI:

Diffusion weighted imaging

EEG:

Electro-encephalography

EBV:

Epstein Barr virus

FLAIR:

Fluid Attenuated Inversion Recovery

GABA:

Gamma-aminobutyric acid

GAD65:

Glutamic acid decarboxylase 65kd

GRE:

Gradient recalled echo

HIV:

Human immunodeficiency virus

HSV:

Herpes simplex virus

Ktrans:

Volume transfer constant

LGI1:

Leucine-rich glioma inactivated-1

mGluR:

Metabotropic glutamate receptor

MP-RAGE:

Magnetization Prepared Rapid Acquisition Gradient Echo

MRI:

Magnetic resonance imaging

MS:

Multiple sclerosis

NHL:

Non-Hodgkin lymphoma

NMDAR:

N-methyl-D-aspartate receptor

NSCLC:

Non-small-cell lung cancer

PCNS-PTLD:

Primary central nervous system posttransplant lymphoproliferative disorder

PET:

Positron emission tomography

PML:

Progressive multifocal leukoencephalopathy

PRES:

Posterior reversible encephalopathy syndrome

RANO:

Response Assessment in Neuro-Oncology

RANO-BM:

RANO for brain metastasis

RANO-LM:

RANO for leptomeningeal metastasis

rCBV:

Relative cerebral blood volume

SCLC:

Small-cell lung cancer

SE:

Spin echo

SPACE:

Sampling Perfection with Application optimized Contrasts using different flip angle Evolution

SPS:

Stiff person syndrome

SWI:

Susceptibility weighted imaging

T1w/T2w/T2∗w:

T1 weighted/T2 weighted/T2∗ weighted

Ve:

Extracellular volume

VGKC:

Voltage-gated potassium channel

References

  • Abrey LE, Batchelor TT, Ferreri AJ, Gospodarowicz M, Pulczynski EJ, Zucca E, Smith JR, Korfel A, Soussain C, DeAngelis LM, Neuwelt EA, O’Neill BP, Thiel E, Shenkier T, Graus F, van den Bent M, Seymour JF, Poortmans P, Armitage JO, Cavalli F, C. N. S. L. C. G. International Primary. Report of an international workshop to standardize baseline evaluation and response criteria for primary CNS lymphoma. J Clin Oncol. 2005;23(22):5034–43.

    Article  Google Scholar 

  • Al-Mansour Z, Nelson BP, Evens AM. Post-transplant lymphoproliferative disease (PTLD): risk factors, diagnosis, and current treatment strategies. Curr Hematol Malig Rep. 2013;8(3):173–83.

    Article  Google Scholar 

  • Chamberlain M, Junck L, Brandsma D, Soffietti R, Ruda R, Raizer J, Boogerd W, Taillibert S, Groves MD, Le Rhun E, Walker J, van den Bent M, Wen PY, Jaeckle KA. Leptomeningeal metastases: a RANO proposal for response criteria. Neuro-Oncology. 2017;19(4):484–92.

    PubMed  Google Scholar 

  • Engh JA, Flickinger JC, Niranjan A, Amin DV, Kondziolka DS, Lunsford LD. Optimizing intracranial metastasis detection for stereotactic radiosurgery. Stereotact Funct Neurosurg. 2007;85(4):162–8.

    Article  Google Scholar 

  • Flanagan EP, Caselli RJ. Autoimmune encephalopathy. Semin Neurol. 2011;31(2):144–57.

    Article  Google Scholar 

  • Furutani K, Harada M, Mawlan M, Nishitani H. Difference in enhancement between spin echo and 3-dimensional fast spoiled gradient recalled acquisition in steady state magnetic resonance imaging of brain metastasis at 3-T magnetic resonance imaging. J Comput Assist Tomogr. 2008;32(2):313–9.

    Article  Google Scholar 

  • Graus F, Delattre JY, Antoine JC, Dalmau J, Giometto B, Grisold W, Honnorat J, Smitt PS, Vedeler C, Verschuuren JJ, Vincent A, Voltz R. Recommended diagnostic criteria for paraneoplastic neurological syndromes. J Neurol Neurosurg Psychiatry. 2004;75(8):1135–40.

    Article  CAS  Google Scholar 

  • Hwang TL, Close TP, Grego JM, Brannon WL, Gonzales F. Predilection of brain metastasis in gray and white matter junction and vascular border zones. Cancer. 1996;77(8):1551–5.

    Article  CAS  Google Scholar 

  • Johnson MD, Powell SZ, Boyer PJ, Weil RJ, Moots PL. Dural lesions mimicking meningiomas. Hum Pathol. 2002;33(12):1211–26.

    Article  Google Scholar 

  • Kerkhof M, Ganeff I, Wiggenraad RGJ, Lycklama ANGJ, Hammer S, Taphoorn MJB, Dirven L, Vos MJ. Clinical applicability of and changes in perfusion MR imaging in brain metastases after stereotactic radiotherapy. J Neuro-Oncol. 2018;138(1):133–9.

    Article  CAS  Google Scholar 

  • Kremer S, Grand S, Remy C, Pasquier B, Benabid AL, Bracard S, Le Bas JF. Contribution of dynamic contrast MR imaging to the differentiation between dural metastasis and meningioma. Neuroradiology. 2004;46(8):642–8.

    Article  CAS  Google Scholar 

  • Kwak HS, Hwang S, Chung GH, Song JS, Choi EJ. Detection of small brain metastases at 3 T: comparing the diagnostic performances of contrast-enhanced T1-weighted SPACE, MPRAGE, and 2D FLASH imaging. Clin Imaging. 2015;39(4):571–5.

    Article  Google Scholar 

  • Lancaster E. The diagnosis and treatment of autoimmune encephalitis. J Clin Neurol. 2016;12(1):1–13.

    Article  Google Scholar 

  • Lin NU, Lee EQ, Aoyama H, Barani IJ, Barboriak DP, Baumert BG, Bendszus M, Brown PD, Camidge DR, Chang SM, Dancey J, de Vries EG, Gaspar LE, Harris GJ, Hodi FS, Kalkanis SN, Linskey ME, Macdonald DR, Margolin K, Mehta MP, Schiff D, Soffietti R, Suh JH, van den Bent MJ, Vogelbaum MA, Wen PY, Response Assessment in Neuro-Oncology Group. Response assessment criteria for brain metastases: proposal from the RANO group. Lancet Oncol. 2015;16(6):e270–8.

    Article  Google Scholar 

  • Piquet AL, Cho TA. The clinical approach to encephalitis. Curr Neurol Neurosci Rep. 2016;16(5):45.

    Article  Google Scholar 

  • Suh CH, Kim HS, Jung SC, Choi CG, Kim SJ. Perfusion MRI as a diagnostic biomarker for differentiating glioma from brain metastasis: a systematic review and meta-analysis. Eur Radiol. 2018;28(9):3819–31.

    Article  Google Scholar 

  • Xu XX, Li B, Yang HF, Du Y, Li Y, Wang WX, Zheng HJ, Gong QY. Can diffusion-weighted imaging be used to differentiate brain abscess from other ring-enhancing brain lesions? A meta-analysis. Clin Radiol. 2014;69(9):909–15.

    Article  Google Scholar 

  • Yuh WT, Tali ET, Nguyen HD, Simonson TM, Mayr NA, Fisher DJ. The effect of contrast dose, imaging time, and lesion size in the MR detection of intracerebral metastasis. AJNR Am J Neuroradiol. 1995;16 (2):373–80.

    CAS  PubMed  Google Scholar 

  • Zacharzewska-Gondek A, Maksymowicz H, Szymczyk M, Sasiadek M, Bladowska J. Cerebral metastases of lung cancer mimicking multiple ischaemic lesions – a case report and review of literature. Pol J Radiol. 2017;82:530–5.

    Article  Google Scholar 

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Correspondence to Marion Smits .

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Smits, M. (2019). CNS Involvement in Non-CNS Tumors. In: Barkhof, F., Jager, R., Thurnher, M., Rovira Cañellas, A. (eds) Clinical Neuroradiology. Springer, Cham. https://doi.org/10.1007/978-3-319-61423-6_61-1

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  • DOI: https://doi.org/10.1007/978-3-319-61423-6_61-1

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  • Print ISBN: 978-3-319-61423-6

  • Online ISBN: 978-3-319-61423-6

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