Lymphohemangioma
Lymphohemangioma is a rare, benign tumor that is characterized by the presence of both lymphatic and blood vessels. It is a type of vascular malformation that primarily affects children and is often present at birth or develops within the first two years of life.
Symptoms[edit | edit source]
The symptoms of lymphohemangioma can vary depending on the location and size of the tumor. Common symptoms include a soft, painless mass that can be felt under the skin, skin discoloration, and swelling. In some cases, the tumor may cause functional impairment or cosmetic concerns.
Causes[edit | edit source]
The exact cause of lymphohemangioma is unknown. However, it is believed to be a result of abnormal development of the lymphatic system and blood vessels during fetal development.
Diagnosis[edit | edit source]
Diagnosis of lymphohemangioma is typically made through a combination of physical examination, medical history, and imaging studies such as ultrasound, MRI, or CT scan. In some cases, a biopsy may be performed to confirm the diagnosis.
Treatment[edit | edit source]
Treatment for lymphohemangioma often involves a combination of surgery, sclerotherapy, and laser therapy. The goal of treatment is to reduce the size of the tumor and alleviate any associated symptoms.
Prognosis[edit | edit source]
The prognosis for individuals with lymphohemangioma is generally good. However, the condition can cause significant morbidity if it interferes with vital structures or functions.
See also[edit | edit source]
Lymphohemangioma Resources | ||
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Contributors: Prab R. Tumpati, MD