Diffuse infantile fibromatosis
Diffuse Infantile Fibromatosis (di-fyooz in-fan-tyl fy-bro-ma-to-sis) is a rare, benign tumor that primarily affects infants and young children. It is characterized by the proliferation of fibrous tissue in various parts of the body, most commonly in the musculoskeletal system.
Etymology
The term "Diffuse Infantile Fibromatosis" is derived from the Latin diffusus meaning "spread out", infantilis meaning "childish", and fibromatosis from the Latin fibra (fiber) and the Greek -ωσις (-osis), indicating a condition of abnormal growth or proliferation.
Symptoms
Symptoms of Diffuse Infantile Fibromatosis may vary depending on the location and size of the tumor. Common symptoms include painless swelling or lump, limited movement in the affected area, and potential deformity if the tumor affects bone structure.
Diagnosis
Diagnosis of Diffuse Infantile Fibromatosis typically involves a combination of physical examination, medical history, and imaging studies such as MRI or CT scan. A biopsy may also be performed to confirm the diagnosis.
Treatment
Treatment options for Diffuse Infantile Fibromatosis include surgery, chemotherapy, and radiation therapy. The choice of treatment depends on the size, location, and aggressiveness of the tumor, as well as the patient's overall health.
Prognosis
The prognosis for Diffuse Infantile Fibromatosis is generally good, as the tumor is benign and does not spread to other parts of the body. However, recurrence is common and long-term monitoring is often necessary.
See Also
References
- Medical references and citations here
External links
- Medical encyclopedia article on Diffuse infantile fibromatosis
- Wikipedia's article - Diffuse infantile fibromatosis
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