Myxoid lipoblastoma
Myxoid lipoblastoma | |
---|---|
Synonyms | |
Pronounce | N/A |
Specialty | Oncology, Pathology |
Symptoms | Painless, soft tissue mass |
Complications | N/A |
Onset | Usually in infancy or early childhood |
Duration | |
Types | |
Causes | Unknown |
Risks | |
Diagnosis | Histopathology |
Differential diagnosis | Lipoma, Myxoid liposarcoma, Fibromatosis |
Prevention | N/A |
Treatment | Surgical excision |
Medication | |
Prognosis | Generally good with complete excision |
Frequency | Rare |
Deaths | N/A |
Myxoid lipoblastoma is a rare type of tumor that typically occurs in infants and young children. It is a benign (non-cancerous) tumor that originates from fat cells. The tumor is characterized by its myxoid (mucous-like) appearance and the presence of lipoblasts, immature fat cells.
Symptoms
The symptoms of myxoid lipoblastoma can vary depending on the location and size of the tumor. Common symptoms may include a painless lump or swelling, discomfort or pain if the tumor is pressing on nearby tissues, and possible changes in body function depending on the tumor's location.
Diagnosis
Diagnosis of myxoid lipoblastoma typically involves a physical examination and imaging tests such as ultrasound, CT scan, or MRI. A biopsy may also be performed to confirm the diagnosis.
Treatment
Treatment for myxoid lipoblastoma usually involves surgical removal of the tumor. In some cases, chemotherapy or radiation therapy may be used if the tumor cannot be completely removed by surgery.
Prognosis
The prognosis for individuals with myxoid lipoblastoma is generally good, as the tumor is benign and does not spread to other parts of the body. However, there is a risk of recurrence, so regular follow-up appointments are necessary.
See also
References
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