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Research ArticleSpine

Intramedullary Spinal Cord Metastases: MRI and Relevant Clinical Features from a 13-Year Institutional Case Series

J.B. Rykken, F.E. Diehn, C.H. Hunt, K.M. Schwartz, L.J. Eckel, C.P. Wood, T.J. Kaufmann, R.K. Lingineni, R.E. Carter and J.T. Wald
American Journal of Neuroradiology October 2013, 34 (10) 2043-2049; DOI: https://doi.org/10.3174/ajnr.A3526
J.B. Rykken
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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F.E. Diehn
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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C.H. Hunt
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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K.M. Schwartz
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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L.J. Eckel
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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C.P. Wood
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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T.J. Kaufmann
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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R.K. Lingineni
bDepartment of Health Sciences Research (R.K.L., R.E.C.), Mayo Clinic, Rochester, Minnesota.
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R.E. Carter
bDepartment of Health Sciences Research (R.K.L., R.E.C.), Mayo Clinic, Rochester, Minnesota.
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J.T. Wald
aFrom the Division of Neuroradiology (J.B.R., F.E.D., C.H.H., K.M.S., L.J.E., C.P.W., T.J.K., J.T.W.), Department of Radiology
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  • Fig 1.
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    Fig 1.

    Multiple intramedullary spinal cord metastases in an asymptomatic patient. A 73-year-old man with a history of metastatic lung adenocarcinoma underwent a spine MR imaging after a PET-CT scan had demonstrated multifocal spinal hypermetabolism. He was asymptomatic with regard to the spinal cord. Postcontrast sagittal T1-weighted images of the cervical (A) and thoracic (B) spine are shown. Multiple intramedullary spinal cord metastases are demonstrated at the C2, T4, T4–5, and T11 levels (arrows in A, B). In this series, several other patients were asymptomatic.

  • Fig 2.
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    Fig 2.

    Typical solitary intramedullary spinal cord metastasis, with visualization of primary tumor. A 66-year-old man presented with 6 weeks of paresthesias, bladder dysfunction, lower extremity weakness, and pain. Thoracic spine sagittal T2-weighted (A), sagittal T1-weighted (B), postcontrast sagittal T1-weighted (C), and axial T1-weighted (D) images are shown. A T2 hyperintense, expansile intramedullary cord lesion (arrow) is associated with a large amount of cord T2 hyperintensity (A). The mass is isointense on T1-weighted images (arrow in B) and enhances heterogeneously (arrow in C). Also noted is a left hilar lung mass (arrows in D), which was further evaluated with chest CT imaging (not shown). This hilar mass was pathologically proved to be a grade 4 undifferentiated small-cell lung carcinoma. Visualization on MR imaging of the primary tumor/non-CNS metastases and/or other spinal/CNS (non–spinal cord) metastases was common in this series.

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    Fig 3.

    Multiple intramedullary spinal cord metastases, with visualization of other CNS metastases. A 60-year-old woman with a history of small-cell lung carcinoma, diagnosed 6.5 months prior, presented with several days of lower extremity weakness and urinary and stool incontinence. MR images of the cervical and thoracic spine with postcontrast fat-saturated consecutive sagittal T1-weighted images of the thoracic spine (A, B, C) and postcontrast sagittal T1-weighted image of the cervical spine (D) are shown. Several enhancing intramedullary lesions are present (white arrows in A, B, D). There is abnormal leptomeningeal enhancement with several small metastases studding the surface of the cord (arrows in C). Metastases are visualized in the lower pons and cerebellum (thick white arrows in D). Visualization on MR imaging of other CNS or spinal (non-spinal cord) metastases was common in this series, and more common in patients with multiple ISCMs.

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    Fig 4.

    Atypical intramedullary spinal cord metastasis with central cystic change/necrosis. A 55-year-old man with recent nephrectomy of a renal cell carcinoma presented with 2 weeks of predominantly left upper extremity pain, paresthesias, and weakness, as well as global hyperreflexia. Cervical spine sagittal T2-weighted (A), T1-weighted (B), and postcontrast fat-saturated T1-weighted images (C), and postcontrast axial T1-weighted image are shown. A mass within the cord at the level of C5 has markedly hyperintense central signal on T2-weighted imaging (A) and corresponding T1 hypointensity (B) consistent with central cystic change/necrosis. The sagittal (C) and axial (D) T1-weighted postcontrast images demonstrate the peripheral enhancement with lack of central enhancement corresponding to the region of central cystic/necrotic change. This represents 1 of only 2 cases in the current series of intramedullary spinal cord metastasis demonstrating cystic/necrotic change. The primary tumor type in the other case (not shown) was lung carcinoma.

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    Fig 5.

    Atypical intramedullary spinal cord metastasis with associated hemorrhage. A 74-year-old man with squamous cell carcinoma of the lung diagnosed 2 years prior presented with 4 weeks of paraplegia. Thoracic spine shown with sagittal T1-weighted (A) and T2-weighted (B) and axial gradient recalled-echo (C) images. Heterogeneous mildly hyperintense central signal is present within the intramedullary spinal cord metastasis on T1-weighted imaging (arrows in A). There is corresponding heterogeneity on T2-weighted imaging (B). The axial gradient recalled-echo image demonstrates corresponding central hypointensity (“blooming,” arrow in C), typical of hemorrhage. This is the only intramedullary spinal cord metastasis in the current series demonstrating signal changes convincing for associated hemorrhage.

Tables

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    Table 1:

    Clinical features of ISCMs, per-patient basis (n = 49 patients)

    FeaturePrevalence
    Sex
        Female26 (53%)
    Primary malignancy
        Lung carcinoma24 (49%)
        Breast carcinoma7 (14%)
        Melanoma5 (10%)
        CNS origin4 (8%)
        Renal cell carcinoma3 (6%)
        Other6 (12%)
    Timing of primary tumor diagnosis
        ISCM presentation preceded primary tumor diagnosis10 (20%)
        ISCM diagnosis preceded primary tumor diagnosis5 (10%)
    Dominant presenting symptoms
        Weakness28 (57%)
        Sensory symptoms8 (16%)
        Bowel and/or bladder dysfunction5 (10%)
        Pain4 (8%)
        Asymptomatic4 (8%)
    Time interval, median (range)
        Duration of symptoms at clinical presentation (n = 44)2 weeks (0.1–32)
        Primary tumor diagnosis to ISCM presentation (n = 38)1.8 years (0–19.3)
        Primary tumor diagnosis to ISCM diagnosis (n = 44)1.6 years (0–19.5)
    • View popup
    Table 2:

    MRI features of ISCMs, per-lesion basis, total of 70 lesions in 49 patients

    FeaturePrevalence
    Location (n = 70)
        Cervical16 (23%)
        Cervicothoracic2 (3%)
        Thoracic40 (57%)
        Thoracic-conus1 (1%)
        Conus11 (16%)
    Position (n = 62)
        Central23 (37%)
        Eccentric35 (56%)
        Exophytic4 (6%)
    Morphology (n = 66)
        Well-circumscribed64 (97%)
        Ill-defined2 (3%)
    Cord expansion (n = 70)
        Present44 (63%)
        Absent26 (37%)
    Enhancement (n = 64)
        Present63 (98%)
        Absent1 (2%)
    Enhancement pattern (n = 63)
        Homogeneous31 (49%)
        Heterogeneous31 (49%)
        Peripheral (ring)1 (2%)
    Size of enhancing lesion, mm, mean (range)
        Anterior-posterior (n = 63)6.5 (1–16)
        Transverse (n = 53)7.3 (2–23)
        Superior-inferior (n = 63)19.9 (2–114)
    Longitudinal extent, No. of vertebral segments, mean (range)
        Length of enhancement (n = 63)1.4 (1–8)
        Length of cord T2 signal hyperintensity (n = 69)4.5 (1–15)
        Ratio, T2 signal/enhancement (n = 63)3.6 (1–14)
    T2 signal intensity (n = 70)
        Hyperintense55 (79%)
        Hypointense1 (1%)
        Isointense14 (20%)
    T1 signal intensity (n = 63)
        Hyperintense10 (16%)
        Hypointense5 (8%)
        Isointense48 (76%)
    Cystic change (n = 70)
        Intratumoral2 (3%)
        Peritumoral0 (0%)
    Intratumoral hemorrhage (n = 70)1 (1%)
    • View popup
    Table 3:

    Additional MRI features of ISCMs on reference MRI, per-patient basis (n = 49 patients)

    FeaturePrevalence
    Solitary ISCM39 (80%)
    Multiple ISCMs10 (20%)
    Non-cord CNS and/or spinal metastasis29 (59%)
    Leptomeningeal metastasis18 (37%)
    Primary tumor and/or non-CNS metastasis29 (59%)
    Non-cord CNS/spinal metastasis OR primary tumor/non-CNS metastasis43 (88%)
    Both non-cord CNS/spinal metastasis AND primary tumor/non-CNS metastasis15 (31%)
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American Journal of Neuroradiology: 34 (10)
American Journal of Neuroradiology
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J.B. Rykken, F.E. Diehn, C.H. Hunt, K.M. Schwartz, L.J. Eckel, C.P. Wood, T.J. Kaufmann, R.K. Lingineni, R.E. Carter, J.T. Wald
Intramedullary Spinal Cord Metastases: MRI and Relevant Clinical Features from a 13-Year Institutional Case Series
American Journal of Neuroradiology Oct 2013, 34 (10) 2043-2049; DOI: 10.3174/ajnr.A3526

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Intramedullary Spinal Cord Metastases: MRI and Relevant Clinical Features from a 13-Year Institutional Case Series
J.B. Rykken, F.E. Diehn, C.H. Hunt, K.M. Schwartz, L.J. Eckel, C.P. Wood, T.J. Kaufmann, R.K. Lingineni, R.E. Carter, J.T. Wald
American Journal of Neuroradiology Oct 2013, 34 (10) 2043-2049; DOI: 10.3174/ajnr.A3526
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