I love it when readers come to me with strange signs and symptoms (or they’re just my own strange ones) and ask me what might be going on. If it’s a reader, as always, I state that Dr. PA is not a real M.D.! Nonetheless, whichever the situation, I get a chance to do some fun research. And sometimes, doing that research makes me feel really stupid. But hey, Dr. PA can’t know everything, right?
When most people think of Status Epilepticus (or just “Status” as we epilepsy folks tend call it) everyone sees an extended tonic-clonic, that if not treated immediately, will result in death. This can actually happen. I’ll explain what does happen, but after that, we need clear up some things.
Now, the pathophysiology of possible death in brief: high levels of neuronal death, marked lowering of blood pressures resulting in heart failure, impairment of breathing plus pulmonary edema, hyperthermia.
Please note that this list may not be exhaustive. The information has been obtained from the Neurology section of Medscape. Also, please note that Status Epilepticus occurs in a large proportion of the population who do not already have epilepsy. Further, to actually die or have brain damage happen, you would have to remain in Status for
On a personal note, I experienced a form of Status several years ago, that did not involve a tonic-clinic seizure. It would be called Simple Partial Status Epilepticus. More specifically, epilepsia partialis continua. I cannot describe how painful it was. My eyes started blinking (no problem, had that before) then my jaw began twitching uncontrollably, my tongue fell out of my mouth and went completely numb so I couldn’t speak. Then, the spasms that were so massive (and SO painful) traveled down my neck and finally through my right arm. This lasted for several hours but eventually went away.
Moving on to what I discovered and knew nothing about. The above are all considered forms of Convulsive Status Epilepticus. There’s something called Non-convulsive Status Epilepticus. How on earth did I miss that over all the years? Well, for one, it is incredibly underdiagnosed, misunderstood, and not even understood at all!
I’ll give you a minute to think. Okay. Guess who might have it? *laughing*
I really do owe it all to said person who got the ball rolling with some questions–just like other readers who have tipped me off to things that may be relevant to me.
It took me a while to go back and read the really, interesting paper I found. I was too focused with a notion that my brain was being typically bizarre, and had simply jumped another hurdle. That notion being, whenever I would have a migraine or become overstimulated due to the Asperger’s, my brain would “think” it had a seizure and then “tell” my body just that.
Here is where I fit in quite nicely in terms of presentation and misdiagnosis. Even Non-Arsey Neuro was impressed and in agreement!
There are also two types but I will not go that far into detail. However, despite already being the messy business it is, the paper does mention that there can be an overlap between both. Now, PA and NCSE:
Presentation: altered neurologic function, diminished cognitive function, aphasia (loss of speech) without altered consciousness or dysarthria (motor problems with speech) atonia (I lose ability to walk and need my cane) visceral sensory disturbance (my heart rate fluctuates in Simple Partial fashion, my stomach can feel like Simple Partial epigastric rising) occasional myoclonus (my legs continue to jerk slightly all the time) migraine with visual aura (rare presentation and I don’t get visual aura much) pre-existing epilepsy.