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  • alexinca
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    Post count: 4

    Dr. Corenman,

    I GREATLY appreciate your thoughtful analysis of the complex problems in my spine. You are the first surgeon to be so thoughtful. Your diagnostic advice makes total sense. I will be contacting the office to take this further in the hope that the pain generator may be better understood, and that there may be something that can be helped.

    Huge Thanks!

    alexinca
    Participant
    Post count: 4

    There are titanium cages between L2 and L4 that fusion bone has grown through (Osteocel was used). Instrumentation used along with the XLIF to accomplish posterior fusion L2-L4 with pedicle screws is what was most recently removed and lab tested for infection. The cages is the only metal at L2-L4 at this point (after posterior screws/rods recently removed, as solid bone fusion has succeeded between those levels). There is still hardware implanted at L4/L5 – irremovable Prodisc-L ADR, and anterior ALIF instrumentation at L5/S1. In the past, L5/S1 had front and back instrumentation after a 360 fusion (due to spondylolisthesis), but posterior hardware was subsequently removed during an attempted decompression (many years ago).

    Pain is constant and very severe. Initially, it was mostly in the legs. Now it is equally terrible in the lower back, upper buttocks, pelvis, and legs. A muscle that connects lower abdomen with the pelvis is constantly in a spasm – like a thick cable. Pain is worsened by sitting and walking. Standing for a short time is better, but the legs are always spasmed and give out. Pain is very severe in bed as well (insomnia). In the past several years, there is more and more pain and spasm in the quads and upper buttocks. This is on top of the previously dominant posterior thigh pain, and hamstring tightness. Back pain has been worsening.

    alexinca
    Participant
    Post count: 4

    The infection in biofilm is Anaerobic 2+ Propionibacterium species.

    The L2-L4 XLIF was reinforced with posterior screws and rods that were most recently removed after the determination of a “solid fusion”. Infection growing on the removed instrumentation was a surprise finding. L5/S1 level had been fused front and back at the time of ADR placement at the level higher. A computer merged report for the SPECT/CT study a year ago said:

    IMPRESSTON:
    1)L1 L2 L3 L4, and L5 and upper sacral-laminectomy defects with partial facetectomv defects and
    incorporation of posterior element bone graft.
    2) posterior fusion hardware with discectomy bridging L2-L3 and L3-L4.
    3) Anterior fusion with discectomy and anterior plate placement at L5-S1.

    4) At L5/S1 there is disc bulge osteophyte complex lateralizing to the neural foramina wiih severe bilateral neural foraminal stenosis L5/S1.
    5) L4-L5 anterior fusion with discectomy and laminectomy defects with moderate to severe bilateral
    neural foraminal stenosis.
    6) There is no significant central canal stenosis.
    There is a 7 degree levoscoliosis L2-L3, L3-L4. There is a 5 mm grade 1 spondylolisthesis L5-S1

    I’ve been told the SPECT/CT has unexplainable multiple “hotspots” (tracer uptake), especially on the left. Left leg, has been progressively worsening: weakness and pain.

    I’m hearing the situation is very complex, the epidural scarring is extensive, and there is a great deal of abnormal extra bone that may be causing stenosis. It is believed the fused levels have been fused well. ADR level evaluation is said to be radiologically limited. Myelogram caused severe multi-month pain flare, and did not have remarkable findings – no central canal stenosis.

    Legs are getting weaker, pain is becoming more unbearable, and I’m losing function.

    I can’t find anyone to help (decompress the nerves, etc.)

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