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20 year old w/spasticity--Possible MS?

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    20 year old w/spasticity--Possible MS?

    Trying to write brief history but not succeeding. My apologies in advance. And advice or insights much appreciated. I posted on another forum but got only advice on nutrition.

    2.5 years ago when 18, daughter, with history of seizures but unmedicated since 16, began complaining of leg weakness. Ped referred to orthopedist, who said bilateral, couldn't be anything wrong. Then came bilateral knee pain, followed by leg pain. Orthopedist continued to say nothing. After a year, she had lower back pain. Again said can't be anything but referred her to physical therapy. Therapist noted tight outer thigh muscles, causing knees to bend in and pigeon toed walk. Difficulty getting up stairs and walking very tiring. Told orthopedist therapist recommended TENS machine. He said she didn't need one so he wouldn't write prescription.

    Last May a sinus infection, accompanied by nausea and vomiting. (This persists to this day, GI investigation negative but she takes Zofran 3 times a day.) Found to have very mild pneumonia and put on Z pack. That week back pain became very strong and walking difficult. Ended up at ER with 105 fever and found to have necrotizing double pneumonia. Hospitalized for six days. Hospital brought in neurologist owing to walking difficulties; found reflexes to be brisk--subtle enough for med students with him to miss. Ordered spinal MRI and said was normal. Attending physician said perhaps somataform disorder. (She has anxiety and had an attack while in hospital.)

    Took her to rehabilitation specialist--disdainful of somatoform dx as he said he felt spasming in back. Personally looked at MRI and found septations at T3/T4 to T7. He called the hospital and made them change the report and told us to go to neurosurgeon. Got there in August. By this time, very hyperreflexive and the neurosurgeon said she was spastic. Negative on Babinski reflex. Didn't look at MRI but said formation in thoracic spine had nothing to do with it--she had MS, vitamin B12 deficiency, lyme or some other infection. Told us to go to neurologist and gave her baclofen--helped enormously with walking, but pain persisted. Had brain MRI--was fine except for two arterial malformations (telangiectasia and DVM--neither dangerous, latter possibly connected to seizures). In October got spinal tap--tested for all kinds of infections, but they ran out of fluid and didn't do oligoclonal bands or the other test (I think Igg?) for MS. What they did test for was fine. Neurologist also ordered tests for genetic disorders like familial spastic paraplegia--all negative--and decided might be autoimmune (PANDAS--she's an expert in this). Got IVIG in November.

    Did okay for a couple of months. Stopped taking Baclophen in early January when prescription ran out. PCP around that time suggested she see neurologist who is known MS expert. Earliest appointment was in July. Around April complaints about leg pain began again but we waited for neuro appointment. First of July UTI with high fever and flank pain--infection going up to kidney. Hospitalized for two days. See neuro ten days later. Doesn't mention MS but looks at MRI and speculates she may have spinal fistula in thoracic spine. Tells her to come back but next appointment in February.

    In meantime, great worsening of leg and back pain, I think because of UTI--always much worse after illness with high fever; often has to walk with a cane. I take her to pain management doctor to get prescription for physical therapy and TENS machine. Last week therapist saw her and was alarmed. Her spasticity is like what he sees in MS patients and he felt MS needed to be excluded as soon as possible and that it was imperative she get back on Baclofen so he could work better with her. He consulted with a pediatric neurologist he knows who said she should get workup as soon as possible, going to the ER if need be. I told the psychiatrist she sees for anxiety (she hadn't mentioned to him) and he said it was possibly psychogenic. He arranged for a consult this week with a colleague who is also qualified in neurology.

    So I have a daughter who is clearly spastic and have three theories of origin: MS, spinal fistula, and psychogenic. In favor of MS--spasticity enough for therapist to raise grave concerns, possibly seizures (hear more common in pwMS), possibly nausea and vomiting (but read contrary things on this). Not sure what an MS episode is like but she fairly often reports bizarre symptoms. Against: hard to get into MS expert didn't mention, no white spots on brain, no Babinski response, probably no eye involvement (she periodically complains about eyes, but then again she sleeps with her contacts in and isn't great at contact hygiene). For spinal fistula: would explain spasticity; against--pretty rare. For psychogenic: has severe anxiety problem and has had at least two episodes of psychogenic seizures (at a much younger age). Against: have been all over the internet and can find no mentions that spasticity or hyperreflexia can be psychogenic.

    Finally, how alarmed should I be in terms of demanding action from doctors who so far have taken a lacksadaisical approach to her issues? The therapist was clearly alarmed as was the neuro he consulted, but none of her doctors have been. This has been going on for over two and half years. She is near the end of her rope--she can't work or go to school because how she feels from one day to the next is so variable and many days she can barely get out of bed--and so am I.

    Much thanks,
    Desperate Mum

    #2
    Hello Desperatemum and welcome to MSWorld.

    I am sorry that your daughter is having such a difficult time with her health.

    but they ran out of fluid and didn't do oligoclonal bands or the other test (I think Igg?) for MS.
    Well, as a mother myself that would really piss me off. Unfortunately, that may be a test to reconsidering doing again (sorry ) and make sure they get enough fluid to check for o-bands (a positive LP with o-bands could help to support a diagnosis of MS).

    If you click on the link below, scroll down and it will explain normal/abnormal results of the LP as well as possible causes for abnormal findings.

    http://www.nlm.nih.gov/medlineplus/e...cle/003428.htm

    Attending physician said perhaps somataform disorder. (She has anxiety and had an attack while in hospital.)

    have been all over the internet and can find no mentions that spasticity or hyperreflexia can be psychogenic.
    Psychogenic problems can cause so many different symptoms.

    Please read the link provided below. This is about conversion disorder. I am not suggesting this is what your daughter has but may need to be explored if testing is not providing any answers.

    I have known a young lady since she was in kindergarten (she is a friend of my daughters they are both 21 years old now). Her parents spent tens of thousands of dollars trying to find answers to their daughter symptoms.

    Starting in about 6th grade she started having difficulty walking (used a wheelchair or walker much of the time), severe headaches and many other problems. She had been diagnosed with RSD and fibromyalgia and then had those diagnosis taken away.

    He mother spoke to me about her symptoms, some of which would fit with MS but not all of them. Many of the symptoms I could personally relate to. I helped her when needed and we did carpooling so I did see the condition she would be in. Then there were times she would do fine for awhile.

    It got to the point were they were her parents were flying her to out-of-state prominent hospital trying to find answers.

    It was heart breaking to see this bright intelligent young lady in her current condition. My family (husband, daughter, son and myself) were angry and shocked when doctors started to bring up a Conversion Disorder as an explination to her symptoms.

    I never once even considered this to be correct and thought it was just a diagnosis to throw at then because the doctors didn't know.

    About 3 years ago things came to a head in other ways and sadly, the conversion disorder was correct. With extensive therapy this young lady is slowly on her way to a happy health life.

    I wanted to share this story as a way to let you know that IF your daughter has a Coversion Disorder it can get better...with help.

    About Conversion Disorder:
    http://www.minddisorders.com/Br-Del/...-disorder.html

    If you have any questions please feel free to post them.

    Take care
    Diagnosed 1984
    “Lightworkers aren’t here to avoid the darkness…they are here to transform the darkness through the illuminating power of love.” Muses from a mystic

    Comment


      #3
      Snoopy,

      Thanks for your reply. Yes I was very upset and when I pointed it out to the lab tech at the hospital she went the extra mile and called all of the four labs the fluid had been sent to checking to see if any extra fluid remained so the test could be done. Unfortunately, none was left; she said the doctor hadn't prioritized the MS tests on the scrip (another lesson learned--who knew it was your job to watch for that?). Quite furious they managed to do the the HIV and STD tests--why waste precious fluid on tests that can be done just as well with blood?

      Re: conversion disorder, I am open to it, although not enthralled. It's a type of somatoform disorder and the prognosis isn't great. Also, by doctors' own admission some 25% to 30% of those who get the dx turn out to have a neurological disorder (many of them MS). Also admit I am a little biased in that I have been quite put off by how quickly doctors go to a psychogenic dx without the proper investigation. Just last week had daughter in ER with continuous and painful head and shoulder jerking and they tried to tell me it was psychogenic because of her anxiety history. I said I was sure it was a side effect from a medication she was taking. After their ativan treatment failed to affect it one bit after three hours (pretty much proving it wasn't anxiety provoked), they finally gave her a shot of medication that counters side effects in the medication in question and the jerking ended in 10 minutes.

      Everything I saw on psychogenic paraplegia says it is can be confirmed by a finding of normal muscle tone and reflexes. But she is clearly spastic and hyperreflexive, so it doesn't seem to fit. Daughter did say she'd rather have a psych dx than an MS dx, although she thinks a psych dx for what she has would be weird.

      The fistula dx would seem better than the other two; it's treatable in a reasonably straightforward way. But what I've read says that the sooner it is treated the better the outcome. I do think we need to get the bottom of this ASAP so treatment can begin--if it's psychogenic, so be it.

      Desperatemum

      Comment


        #4
        I am so sorry about your daughter, no matter what the cause.

        I agree also about getting another lumbar puncture to check for o bands.

        I hope you both find some answers soon.

        Comment


          #5
          Misslux, thank you for your good wishes.

          The PT saw daughter again today (much improved in ability to move around since his last visit). I told him the neurogenic theory and he believes it is impossible. She has spasticity in her adductor muscles and hamstrings, as well as ankle clonus, all indicative in his words of "neurological damage." He is still on the MS line of thinking.

          He'll send me an email with his observations so that I can show them to the neuro she's seeing tomorrow.

          Comment


            #6
            Hi Desperatemum,

            There are no symptoms that are unique to MS. People with MS have spasticity but so do people with other neurological problems. MS isn't diagnosed from symptoms. Your daughter's PT knows that spasticity is a sign of MS but it sounds like he's trying to diagnose from symptoms alone.

            Your daughter has already had MRI's that don't show damage that's characteristic of MS. Spinal septations and fistulas are not MS. The diagnostic criteria for MS require lesions on MRI that are characteristic of MS and your daughter apparently doesn't have them. That alone is going to make it very difficult for her to get a diagnosis of MS.

            The diagnostic criteria also require at least two episodes or "attacks" that are characteristic of demyelination. It doesn't sound like your daughter has had those either. And it isn't typical for MS to present as spasticity and widespread pain without other signs and symptoms of MS. And isn't typical for that to go on for years without other signs and symptoms of MS and no signs of MS on MRI. That's many things that point away from MS.

            From what you've said your daughter's tests and history don't indicate MS. All she has is indications of neurological damage that could come from all kinds of things. Her epilepsy already puts her at risk of neurological problems. There's evidence of a spinal cord abnormalities that could cause the spasticity. Spasticity is common after spinal cord injury or with other spinal cord damage. What your daughter doesn't have is evidence of MS. Her PT can comment all he wants to about her physical condition but none of it overrules the current lack of medical evidence for MS. Again, a generic symptom isn't medical evidence for a specific condition.

            Symptoms in common with general neurological damage from other conditions don't add up to MS. It makes more sense to go with the evidence - spinal cord fistulas or septations and possible additive epileptic damage - than it does to ignore the obvious and start pursuing things that evidence already doesn't support, like MS.

            If you want to keep looking to rule in/out MS your daughter will have to have other tests that her neurologist might be hesitant to do since her MRI's and history already don't point to MS. As awful as it might be, another lumbar puncture will have to be done to look for O-bands and myelin specific antibodies. And she'll have to have visual and somatosensory evoked potentials, maybe even an auditory evoked potential, to look for signs of demyelination. And if you want to cover all the bases, she should probably have an EMG to look for other causes of spasticity.

            And even if your daughter doesn't have conversion disorder, her anxiety isn't helping. Anxiety adds a psychological component that makes physical problems and their effects even worse. It's good that she's seeing a psychiatrist but if she still can't control her anxiety it might be time for her to change doctors to try to find one who can actually help her get it under control. With all of her challenges a "pretty good" grip on anxiety isn't good enough.

            And if you can't find a doctor who seems to be taking her problems seriously, there's always the option of another medical opinion.

            I hope you both come up with some good answers soon.

            Comment


              #7
              MSer102,

              Great post. Personally I too am dubious about the MS dx for all the reasons you say. I am grateful to the PT, however, for registering alarm about her spasticity--something none of the doctors have done. I did a lot more reading after the PT and it has given me the confidence to tell doctors it is not okay to be complacent about this symptom--it's important to get to the underlying cause as soon as possible because for a number of causes (eg spinal fistula) the quality of outcome depends on how promptly they are treated.

              I am pretty sure she'll need another LP and not just to rule out MS --perhaps it is a sign of her own desperation that she's said she'll do another--and this will be her third. She had one in the ER last year when they suspected she had meningitis (luckily just the aseptic variety).

              Yes the anxiety isn't helping--not sure how much good the meds she is on are doing. My choice would be none, but she likes her psychiatrist so I am loath to change. Also, he personally scheduled the neurology consult--something I value very highly as it shows a level of concern that I have encountered all too rarely.

              Desperatemum

              Comment


                #8
                Keep fighting and being proactive to find out what is wrong.
                It may not show up right away, but will in time.

                Your daughter is NOT imagining all of this. MS though, is very hard to diagnose and to treat.

                It also may not be MS.

                Good Luck and hugs.

                Comment

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