Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Spinal tumor
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
{{Short description|Neoplasms located in either the vertebral column or the spinal cord}} '''Spinal tumors''' are [[neoplasm]]s located in either the [[vertebral column]] or the [[spinal cord]].<ref name=":0">{{Cite book |editor1-last=Arnautović |editor1-first=Kenan I. |editor2-last=Gokaslan |editor2-first=Ziya L. |year=2018 |title=Spinal Cord Tumors |location=Cham, Switzerland |publisher=Springer |isbn=978-3-319-99438-3 |oclc=1084270205}}</ref> There are three main types of spinal tumors classified based on their location: extradural and intradural (intradural-intramedullary and intradural-extramedullary). Extradural tumors are located outside the [[dura mater]] lining and are most commonly [[Metastasis|metastatic]].<ref name=":3">{{Citation|last1=Gossman|first1=William|title=Cancer, Intramedullary Spinal Cord Tumors|date=2019|url=http://www.ncbi.nlm.nih.gov/books/NBK442031/|work=StatPearls|publisher=StatPearls Publishing|pmid=28723060|access-date=2019-12-03|last2=Hoang|first2=Stanley|last3=Mesfin|first3=Fassil B.}}</ref> Intradural tumors are located inside the dura mater lining and are further subdivided into intramedullary and extramedullary tumors. Intradural-intramedullary tumors are located within the dura and spinal cord parenchyma, while intradural-extramedullary tumors are located within the dura but outside the spinal cord parenchyma. The most common presenting symptom of spinal tumors is nocturnal back pain.<ref name=":0" /> Other common symptoms include [[muscle]] weakness, sensory loss, and difficulty walking.<ref name=":0" /> Loss of bowel and [[Urinary bladder|bladder]] control may occur during the later stages of the disease.<ref name=":4">{{Cite journal|last=Balériaux|first=D. L. F.|date=1999-08-01|title=Spinal cord tumors|journal=European Radiology|language=en|volume=9|issue=7|pages=1252–1258|doi=10.1007/s003300050831|pmid=10460357|s2cid=6586168|issn=1432-1084}}</ref> The cause of spinal tumors is unknown. Most extradural tumors are metastatic commonly from breast, prostate, lung, and kidney cancer.<ref name=":1">{{Citation|last1=Burton|first1=Matthew R.|title=Cancer, Conus and Cauda Equina Tumors|date=2019|url=http://www.ncbi.nlm.nih.gov/books/NBK441878/|work=StatPearls|publisher=StatPearls Publishing|pmid=28722908|access-date=2019-12-03|last2=Mesfin|first2=Fassil B.}}</ref> There are many genetic factors associated with intradural tumors, most commonly [[Neurofibromatosis type I|neurofibromatosis 1]] (NF1), [[Neurofibromatosis type II|neurofibromatosis 2]] (NF2), and [[Von Hippel–Lindau disease|Von Hippel–Lindau]] (VHL) syndrome.<ref name=":0" /> The most common type of intradural-extramedullary tumors are [[meningioma]]s and [[Nerve sheath tumor|nerve-sheath tumors]].<ref name=":2">{{Cite web|url=https://www.aans.org/|title=Spinal Tumors – Types, Symptoms, Diagnosis and Treatment|website=www.aans.org|language=en|access-date=2019-12-03}}</ref> The most common type of intradural-intramedullary tumors are [[ependymoma]]s and [[astrocytoma]]s.<ref name=":5">{{Cite journal|last1=Mechtler|first1=Laszlo L.|last2=Nandigam|first2=Kaveer|date=2013-02-01|title=Spinal Cord Tumors: New Views and Future Directions|journal=Neurologic Clinics|series=Spinal Cord Diseases|volume=31|issue=1|pages=241–268|doi=10.1016/j.ncl.2012.09.011|pmid=23186903|issn=0733-8619}}</ref> Diagnosis involves a complete medical evaluation followed by imaging with a CT or MRI. A biopsy may be obtained in certain cases to categorize the lesion if the diagnosis is uncertain.<ref name=":0" /><ref name=":1" /><ref name=":2" /> Treatment often involves some combination of surgery, radiation, and chemotherapy.<ref name=":0" /><ref name=":1" /><ref name=":2" /> Observation with follow-up imaging may be an option for small, benign lesions.<ref name=":1" /> Steroids may also be given before surgery in cases of significant cord compression.<ref name=":0" /> Outcomes depend on a number of factors including whether the tumor is benign or malignant, primary or metastatic, and location of the tumor. Treatment is often [[Palliative care|palliative]] for the vast majority of metastatic tumors.<ref name=":2" />
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)