Sacral Tumors

Sacral Tumors

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The sacrum is a large triangular bone at the lower end of the spine connecting the pelvis to the spine. Tumors developing in this region are rare but complex to diagnose and treat. Sacral tumors can be primary (starting here) or metastatic (spreading from other organs).

What Is a Sacral Tumor?

Types of Sacral Tumors

Primary Tumors

  • Chordoma: The most common primary tumor arising from notochord remnants. Grows slowly but is locally aggressive.
  • Giant cell tumor: Locally aggressive, benign character
  • Chondrosarcoma: Malignant tumor from cartilage
  • Osteosarcoma: Malignant bone tumor
  • Ewing sarcoma: Seen in young patients
  • Schwannoma: Benign nerve-origin tumor
  • Sacral meningioma: Rarely seen
Sacral Tumors - Prof. Dr. Salim Şentürk

Metastatic Tumors

Spread from prostate, breast, lung, kidney, and thyroid cancers is common.

Symptoms

  • Low back and hip pain: Slow onset, progressive
  • Radiating leg pain: Sciatica-like
  • Mass in sacral region: Palpable swelling
  • Bladder dysfunction: Incontinence, retention
  • Bowel dysfunction: Constipation, incontinence
  • Sexual dysfunction: Erectile dysfunction
  • Leg weakness: Due to nerve compression
  • Perineal numbness: Saddle anesthesia

Diagnosis

  • Pelvic MRI: Tumor size, extent, nerve and organ involvement
  • CT scan: Bone destruction assessment
  • PET-CT: Metastasis screening
  • Biopsy: Tissue sample for histopathological diagnosis
  • Angiography: Preoperative embolization planning for vascular tumors

Treatment

Surgical Treatment

Primary treatment method is surgical resection:

  • En bloc resection: Removal of tumor with healthy tissue margins
  • Posterior approach: For tumors below S3
  • Combined anterior-posterior approach: For large tumors
  • Sacrectomy: Partial or total removal of sacrum

Surgical Challenges

  • Preserving sacral nerve roots
  • Preserving bladder and bowel function
  • Proximity to major blood vessels
  • Maintaining pelvic stability

Radiotherapy

  • As adjunct to surgery or alone
  • Proton therapy (effective for chordoma)
  • Carbon ion therapy

Chemotherapy

Used for Ewing sarcoma and some metastatic tumors.

Post-Operative Care

  • Hospital stay: 7-14 days
  • Rehabilitation: Intensive physical therapy
  • Bladder/bowel training: If function is lost
  • Follow-up: Regular MRI checks

Prognosis

Prognosis depends on tumor type and surgical margins. Five-year survival for chordoma with en bloc resection is 60-80%. For metastatic tumors, treatment is palliative.

Why Choose Prof. Dr. Salim Şentürk?

Prof. Dr. Salim Şentürk has multidisciplinary approach and complex surgical experience in sacral tumor surgery.

Sacral Mass Evaluation

Schedule an appointment for tumor type determination with MRI and biopsy.

Frequently Asked Questions

Can I walk after sacral tumor surgery?

Depends on nerve preservation. Leg function is usually preserved in high sacral tumors.

Will my bladder function be affected?

Bladder dysfunction may develop depending on S2-S4 nerve root involvement. Adaptation is achieved with rehabilitation.

Reviewed by: Prof. Dr. Salim Şentürk, Neurosurgeon

Last updated:

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