Atypical teratoid rhabdoid tumor surgery

Atypical teratoid rhabdoid tumor Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Atypical Teratoid Rhabdoid Tumor from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Study of Choice
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X-ray
Echocardiography and Ultrasound
CT scan
MRI
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Atypical teratoid rhabdoid tumor surgery On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Atypical teratoid rhabdoid tumor surgery All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Atypical teratoid rhabdoid tumor surgery
CDC on Atypical teratoid rhabdoid tumor surgery
Atypical teratoid rhabdoid tumor surgery in the news
Blogs on Atypical teratoid rhabdoid tumor surgery
Directions to Hospitals Treating Atypical teratoid rhabdoid tumor
Risk calculators and risk factors for Atypical teratoid rhabdoid tumor surgery

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Surgery

Surgery plays a critical role in obtaining tissue to make an accurate diagnosis. Surgery alone is not curative. In addition, 30% of the AT/RTs are located supratentorially and there is a predilection for the cerebello-pontine angle which makes surgical resection difficult. One-third or more children will have disseminated disease at the time of diagnosis. Total or near-total resections are often not possible.