Connective Tissue Tumors: Fibroma, Fibromatosis, Fibrosarcoma

Connective Tissue Tumors: Fibroma, Fibromatosis, Fibrosarcoma
Learn more about connective tissue tumors.

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Definition

A tumor is an abnormal growth of tissue that can either be benign (non-cancerous) or malignant (cancerous). Tumors develop when cells in the body begin to divide uncontrollably. In the case of connective tissue tumors, these abnormal growths form in the tissue that binds and supports other body parts, including tendons, ligaments, skin, cornea, and bones.

Connective tissue tumors, such as fibromas, fibromatosis, and fibrosarcoma, occur when fibroblasts (young connective tissue cells) grow excessively. Fibromas are generally benign, but they can lead to more severe forms, such as fibromatosis (multiple fibromas) or fibrosarcoma (malignant fibromas). These tumors can develop at any age and may occur in various parts of the body.

Fibroma is a benign tumor that originates from fibroblasts. These tumors can occur in virtually any organ of the body, as fibroblasts are present throughout. Most cases of fibromas do not require specific treatment unless they develop into fibromatosis or fibrosarcoma. Fibromatosis refers to the development of multiple fibromas that may grow and spread to other areas. This condition can cause more severe symptoms and may require treatment. Fibrosarcoma is a malignant form of fibroma that arises from the connective tissue and can spread to other parts of the body. Unlike fibromas, fibrosarcomas can be life-threatening if not treated.

Types of Connective Tissue Tumors:

  • Plantar fibromas, these fibromas appear on the soles of the feet and can cause discomfort while walking.
  • Non-ossifying fibromas, benign bone tumors that affect 20% to 40% of children, usually causing no symptoms and often resolving on their own.
  • Angiofibromas tumors originate from blood vessels and connective tissue and may appear on the skin or mucosal surfaces.
  • Dermatofibromas are benign tumors that typically appear on the skin.
  • Oral fibromas that develop in the mouth, often on the gums or other oral tissues.

 

Causes

Tumors generally develop when cells in the body grow and divide excessively, leading to an imbalance between the formation of new cells and the death of old cells. Certain types of tumors, including fibromas, may also be linked to viral infections such as Epstein-Barr virus, human papillomavirus, hepatitis B, and hepatitis C. In some cases, fibroma tumors can result from hormonal imbalances in the body.

The exact cause of fibrosarcoma remains unclear. However, several inherited conditions have been found to increase the risk of developing fibrosarcoma, including:

  • Neurofibromatosis type 1

  • Nevoid basal cell carcinoma syndrome

  • Retinoblastoma

  • Tuberous sclerosis

  • Werner syndrome

 

Risk Factor

There are several risk factors that can contribute to the development of connective tissue tumors:

  • Individuals with compromised immune systems, such as those with HIV/AIDS or autoimmune diseases like systemic lupus erythematosus and rheumatoid arthritis, are at higher risk.

  • Exposure to chemicals and toxins

  • Excessive sun exposure

  • Radiation exposure

  • Viral infections

  • Family history of cancer

  • Obesity

  • Excessive alcohol use

  • Smoking

  • Older age

 

Symptoms

The initial appearance of connective tissue tumors is often not noticeable, as they typically form in deeper connective tissue. These tumors may only become apparent once they grow large enough. The specific symptoms depend on the type and location of the tumor.

For example:

  • A tumor located on the leg may cause a noticeable lump and pain when standing or walking.

  • If the tumor is on the skin, it may cause swelling and tenderness, especially if it is large.

A key difference between fibroma and fibromatosis is the number of tumors. If a single tumor is present, it is referred to as a fibroma. If multiple tumors are present, the condition is called fibromatosis. In malignant cases, such as fibrosarcoma, the tumor is often accompanied by systemic symptoms, such as:

  • Unexplained weight loss

  • Changes in skin texture (becoming darker and drier)

  • Rapid tumor enlargement

 

Diagnosis

The diagnosis of connective tissue tumors involves a detailed medical history, physical examination, and various diagnostic tests.

Medical Interview

During the medical interview, the doctor will ask several questions to gather relevant information:

  • Current symptoms

  • Duration of symptoms

  • Personal medical history

  • Family medical history

  • Occupational and lifestyle factors

 

Physical Examination

The doctor will conduct a physical examination starting with a general health check, which includes measuring blood pressure, body temperature, pulse, and respiratory rate. If the tumor is visible, the doctor will perform a more specific examination of the lump, feeling for its size, shape, consistency, and color.

The examination may include:

  • Palpating the lump to assess for pain, temperature differences, and the boundaries of the tumor.

  • Checking for any abnormalities in surrounding tissues.

 

Diagnostic Tests

To further confirm the diagnosis, the doctor may recommend additional tests, including:

  • Laboratory Tests
    Routine blood tests may be ordered to rule out other conditions. A biopsy might also be performed, where a sample of the tumor is taken and examined under a microscope.

  • Imaging Tests
    Depending on the tumor’s location, the doctor may suggest imaging tests such as:

    • Ultrasonography (USG)

    • X-rays

    • Bone Scans

    • CT Scans

    • Magnetic Resonance Imaging (MRI)

 

Management

The management of connective tissue tumors varies depending on whether the tumor is benign or malignant.

Benign Tumors

Benign connective tissue tumors, such as fibromas and fibromatosis, often resolve on their own and generally do not require aggressive treatment. However, if their growth starts interfering with daily activities or causing discomfort, treatment may be necessary based on the tumor's size and location. Common treatments for benign tumors include:

  • Pain relievers
  • Corticosteroid injections
  • Cryotherapy
  • Laser therapy or dermabration
  • Surgery for large tumors

 

Malignant Tumors

Malignant connective tissue tumors, such as fibrosarcomas, require more intensive treatment due to their aggressive nature. Treatment for malignant tumors typically involves surgical procedure, radiation therapy, and/or chemotherapy.

 

Complications

A common complication of connective tissue tumors is the progression from benign to malignant, leading to cancer. If left untreated, this transition can be life-threatening. Additionally, as tumors grow, they can interfere with daily activities, causing pain or difficulty with movement. When a large malignant tumor occurs in or near vital organs, it can be life-threatening if not treated effectively and promptly.

 

Prevention

While there is no surefire way to prevent connective tissue tumors, adopting a healthy lifestyle and reducing known risk factors can help lower the chances of developing these tumors. Maintaining a healthy weight through a balanced diet can help reduce the risk of obesity, which is associated with various types of tumors.

Limit exposure to carcinogens such as excessive radiation, toxic chemicals, and cigarette smoke. Reducing alcohol consumption can also lower the risk of cancer. Knowing your family’s medical history, especially a history of cancer, can help assess your risk of developing malignant tumors. Regular screenings may be recommended for individuals with a family history of cancer.

 

When to See a Doctor?

If you notice a lump that does not go away or continues to grow, or if you experience drastic weight loss within a short period, it is important to see a doctor immediately. A general practitioner can perform an initial evaluation to determine whether the lump is benign or malignant and decide whether further treatment is necessary.

 

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Writer : dr Lovira Ai Care
Editor :
  • dr Hanifa Rahma
Last Updated : Thursday, 24 July 2025 | 23:39

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