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Whole-Body MRI for Oncology Screening

Radiation-free comprehensive cancer screening and staging.

Written by: Saygı Hospital Health Guide Editorial Board
Last updated:

This content has been compiled by the Saygı Hospital Health Guide Editorial Board and is periodically reviewed by a specialist physician.

References (5)

This content is for informational purposes only and does not constitute medical advice. You can book an appointment at our Radyoloji department. Book Appointment →

What is Whole-Body MRI for Oncology Screening?

Whole-body MRI (WB-MRI) is a comprehensive imaging examination that scans the entire body in 30-60 minutes using parallel imaging, multistation acquisition and diffusion-weighted whole-body imaging with background body signal suppression (DWIBS) on 1.5T or 3T scanners.

It provides high-resolution anatomical and functional information without ionizing radiation, making it ideal for repeated screening in hereditary cancer syndromes (Li-Fraumeni, MEN1, BRCA1/2 carriers), pediatric oncology surveillance, multiple myeloma staging and metastatic disease assessment.

Symptoms

Hereditary cancer syndrome screening protocol
Pediatric oncology long-term surveillance
Multiple myeloma initial staging
Suspected occult primary malignancy
Bone metastasis evaluation when bone scan equivocal
Lymphoma response assessment in young patients

Risk Factors

Li-Fraumeni syndrome (TP53 mutation)
Multiple endocrine neoplasia (MEN1, MEN2)
Hereditary BRCA1/2 mutation carriers
Lynch syndrome with high-risk features
Survivors of childhood cancer with high cumulative radiation
Family history of multiple cancers in first-degree relatives

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Confirmed germline cancer predisposition syndrome
  • Pediatric long-term cancer survivor surveillance
  • Newly diagnosed multiple myeloma for staging
  • Symptoms suggesting metastatic disease without primary site
  • Periodic surveillance in known cancer with elevated tumor markers

Treatment Methods

01
Multistation T1, T2 and DWIBS sequences without contrast (radiation-free)
02
1.5T or 3T scanner with multichannel surface coils
03
Annual surveillance for hereditary syndromes (Li-Fraumeni: from age 18)
04
Lesion characterization with focused targeted MRI sequences
05
Multidisciplinary team review for incidental findings
06
Genetic counseling and surveillance protocol planning
07
Targeted biopsy or PET-CT for indeterminate lesions

Which Department to Visit?

You can visit our Radyoloji department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.

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Health Disclaimer: The information on this page is prepared for general informational purposes only. It does not replace medical diagnosis and treatment. Please consult your physician for your complaints. Saygı Hospital does not accept responsibility for actions taken based on the information on this page.