Hamartoma is a tumor-like deformity formed during the development of human organs due to the incorrect combination and arrangement of normal tissues. This tumor is not a true tumor. It grows slowly and increases with the development of the human body. However, it stops growing after reaching a certain size, keeps in harmony with the human body, and rarely becomes malignant. Hamartoma can occur in many organs, such as the lungs, kidneys, breasts, liver, etc. Pulmonary hamartomas are usually tumors formed when bronchial tissue inverts and falls off during embryonic development and is surrounded by normal lung tissue. Renal hamartomas, also known as renal angiomyolipomas, are benign tumors composed of abnormally proliferating blood vessels, smooth muscles, and adipose tissue. Bile duct hamartomas are hamartomas caused by impaired transformation of the bile duct plate into the bile duct during embryonic development. The specific cause of hamartoma is still unclear, but it may be related to family history or some unknown factors affecting embryonic development. The clinical symptoms of hamartoma vary depending on the location of occurrence. Pulmonary hamartoma may present with cough, sputum, hemoptysis, etc., while renal hamartoma may cause back pain and hematuria. In terms of treatment, the treatment of hamartomas depends on their type and size. Some small hamartomas may not require treatment, just regular follow-up. Larger hamartomas, especially those that cause symptoms or rupture, may require surgical removal or embolization. Renal hamartomas smaller than 4 cm may not require treatment, but close follow-up is required; those larger than 4 cm may need to be treated with embolization or surgical removal. Hamartoma is a relatively common benign lesion with a good prognosis in most cases, but appropriate treatment measures need to be taken according to the specific circumstances. |
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