Jump to content
helplinedonate
  • Announcements

    • ForumAdmin

      Frequently Asked Questions - Step by step guides

      Do you need assistance registering, logging in, posting, etc? Please visit the all new Frequently Asked Question Forum for step-by-step guides. Click the link below to access these helpful guides. Frequently Asked Questions
    • ForumAdmin

      Recursos Nuevos en Español

      http://www.parkinson.org/ayuda   http://www.parkinson.org/espanol    
    • ForumAdmin

      Línea de Ayuda 1-800-473-4636

      Línea de Ayuda 1-800-473-4636   ¿Qué es la línea de ayuda 1-800-4PD-INFO (473-4636) de la Fundación Nacional de Parkinson? Es un número de teléfono gratuito que ayuda a las personas con la enfermedad de Parkinson, sus familiares, amigos y profesionales de salud, a solucionar diferentes inquietudes.   La línea de ayuda ofrece: Información actualizada Apoyo emocional Referidos a profesionales de salud Recursos comunitarios Amplia variedad de publicaciones gratis    

Search the Community

Showing results for tags 'craniopharyngioma'.



More search options

  • Search By Tags

    Type tags separated by commas.
  • Search By Author

Content Type


Forums

  • Forum Information
    • Discussion Corner Announcements
    • NPF Forum Member Service Center
    • Frequently Asked Questions - How Do I...???
  • Medical Questions
    • Ask The Doctor
    • Ask The Surgical Team
    • Ask about Nutrition
    • Ask the Pharmacist
    • Pregúntele al Médico
    • Talk To A Speech Clinician
  • Unmoderated Discussion
    • Open Forum
    • Newly Diagnosed
    • Caregivers Forum
    • Young Onset Forum
    • DBS Forum

Found 1 result

  1. I'm a 43-year-old woman who just recently started exhibiting symptoms consistent with Parkinsonism. In 1999, I was diagnosed with what was either an atypical non-functioning pituitary macroadenoma -or- an atypical craniopharyngioma (my doctors settled on calling it the former, but it had characteristic of both). The tumor measured 1" x 0.75", and it was surgically removed via the transspheniodal approach. My question - Is it physically possible that my tumor had pressed against my substantia nigra? I've been trying to find a good brain diagram that shows the substantia nigra in relation to the pituitary (or optic chasm), but I can't seem to find one that clearly shows both regions. From the diagrams I *have* found, I believe there's bone between the two regions. That said, the pressure of my tumor did create a hole in my sphenoid sinus bone, so it seems conceivable that it could have eroded the posterior bone to the point that it was thin enough for pressure to be felt on its other side... but I'm just guessing. My thought is that *perhaps* nature intended for me to get PD later in life, and thus my dopamine-producing cells have just recently started to die off slowly. It would have normally taken decades to reach the 80% cell death point where symptoms start to show, but because the pressure of my tumor caused, say, 70% of the cells to die prematurely, I only had to lose 10% of them "naturally" before exhibiting symptoms. Does my "theory" have any scientific merit? I realize I may be trying to connect unrelated dots. It just seems too coincidental that I'd have two non-related brain issues at my relatively young age, but such things do happen. Thanks in advance for your kind help! P.S. I doubt that taking a dopamine agonist earlier in life would cause Parkinsonism later on, but I'll just add that I *did* take bromocriptine for six months in a "hail Mary" effort to shrink my tumor a little bit before surgery. My prolactin was slightly high so my docs thought the tumor *might* be a wimpy prolactinoma. Of course it wasn't, so the tumor didn't shrink. Instead, compression of my pituitary stalk wasn't letting enough dopamine through (and therefore it wasn't inhibiting as much prolactin as it should have been).
×