Connective Tissue Cancer (Sarcoma): Symptoms, Causes, Diagnosis and Treatment
General Overview
What is Connective Tissue Cancer?
Connective tissue cancer (sarcoma) is a malignancy arising in soft tissue or bone – both of which provide structural support for the body. Soft tissue includes:
- Muscles
- Fat
- Tendons
- Ligaments
- Blood vessels
- Nerves
Although rare, sarcomas represent about 15% of childhood cancers and only about 1% of adult cancers. In the U.S., approximately 16,000 sarcoma cases are diagnosed annually, including around 4,000 bone sarcomas and 13,000 other soft-tissue sarcomas.
Symptoms of Connective Tissue Cancer
Signs and Symptoms
Clinical presentation varies by tumor location. Some tumors cause no noticeable symptoms early on. A soft-tissue sarcoma may initially appear as a painless lump under the skin. As it enlarges, it may compress adjacent organs and cause pain.
Common symptoms include:
- A new lump or mass
- Pain in the limbs, abdomen, or pelvis
- Limited range of motion or difficulty moving the affected area
- Unexplained weight loss
- Back pain
- Pain worsening at night

Potential Complications
Complications may result from local compression or metastasis. Treatment-related side effects from chemotherapy and radiation may include:
- Bone marrow suppression
- Mucositis
- Hair loss
- Fatigue
- Nausea and vomiting
- Hemorrhagic cystitis
- Kidney damage
- Central nervous system toxicity
- Elevated liver enzymes
- Hypertension
- Subcutaneous fibrosis
- Reduced mobility
- Lymphedema
When to See a Doctor
Seek medical attention if you notice any unusual lumps or persistent pain, especially bone pain or back pain that worsens at night. Early evaluation increases the chance of effective treatment.
Causes of Connective Tissue Cancer
Sarcomas develop when immature cells in bone or soft tissue acquire DNA mutations leading to uncontrolled growth and tumor formation. These cells may invade nearby tissue or spread via the bloodstream or lymphatic system (metastasis). The exact triggers that cause a healthy cell to become cancerous remain unclear.
Risk Factors for Connective Tissue Cancer
Who Is at Risk?
Sarcoma can affect both children and adults.
- Soft-tissue sarcomas more often affect adults.
- Bone sarcomas are more common in children, adolescents, and adults over 65.
- Bone sarcomas occur more frequently in males and in Black or Hispanic populations.

Risk-Enhancing Factors
Chemical exposure: Arsenic; certain plastics (vinyl chloride monomer); herbicides (phenoxyacetic acid); wood preservatives (chlorophenols).
Radiation exposure: High-dose radiation from previous cancer treatment.
Chronic lymphedema: Long-term swelling of the arms or legs.
Genetic disorders: Gardner syndrome, Werner syndrome, von Hippel-Lindau disease, Gorlin syndrome, tuberous sclerosis, Li-Fraumeni syndrome, retinoblastoma, and neurofibromatosis type 1.
Diagnosis of Connective Tissue Cancer
Diagnosis begins with a thorough physical examination and review of personal and family medical history. Tests may include:
- X-ray: Detects bone lesions.
- CT scan: Produces cross-sectional images of bone and soft tissue lesions.
- MRI: Offers detailed imaging when abnormalities are suspected on X-ray or CT.
- Bone scan: Evaluates bone disorders such as osteosarcoma.
- PET-CT: Identifies tumors in various body regions.
- Biopsy: Confirms diagnosis by analyzing tissue samples for sarcoma cells.

Treatment of Connective Tissue Cancer
Management is multidisciplinary, involving oncologists, surgeons, pharmacists, and nurses. In pediatric cases, pediatric oncologists are essential. Treatment depends on tumor size, stage, sarcoma type, and overall health. It usually combines medical therapy and surgery.
Medical Treatments
Radiation therapy: High-energy X-rays destroy cancer cells while sparing healthy tissue.
Chemotherapy: Slows cancer cell growth. May be given before surgery (neoadjuvant) or after surgery (adjuvant). Sometimes combined with radiation therapy.
Targeted therapy: Attacks cancer-specific pathways with minimal harm to healthy cells.
Immunotherapy: Boosts the immune system to fight cancer more effectively.

Surgical Treatment
Surgery aims to remove cancer cells while preserving as much healthy tissue as possible. Reconstructive surgery may be needed to restore function. Limb-sparing procedures may involve removing the tumor and replacing the affected bone or joint with metal implants. In some cases, amputation may be necessary—a difficult but sometimes lifesaving decision.
Lifestyle and Prevention
Healthy Habits During and After Treatment
Rehabilitation programs: Help restore function after surgery.
Regular follow-up visits: Monitor for recurrence with physical exams, blood tests, and imaging. Initially monthly, then less frequent as risk decreases.
Nutrition: Work with your doctor or a dietitian to ensure adequate nutrition tailored to your needs.
Physical activity: Gentle exercise can maintain mobility and improve well-being.
Psychological support: Counseling and support groups help cope with the emotional impact of sarcoma treatment.

Prevention Strategies
Currently, no specific method exists to prevent sarcoma because its causes are not fully understood. Regular health check-ups and self-monitoring for changes in your body are essential. Early detection and treatment greatly improve prognosis compared to late diagnosis.