How to treat hamartoma so that it heals quickly

How to treat hamartoma so that it heals quickly

No matter what disease occurs, people’s first thought is definitely to cure it as soon as possible. If it is a simple minor illness, it goes without saying that the cure is very fast. However, if it is a more difficult to treat disease such as a tumor or cancer, what method can be used to cure it quickly? So today we will learn how to treat hamartoma so that it can heal quickly.

Hamartoma refers to a tumor-like deformity caused by the incorrect combination and arrangement of normal tissues in a certain organ of the body during development. Hamartoma can come from many tissues, and is commonly found in the lung (mixed with cartilage islands, bronchial epithelium and glands, localized hyperplasia to form localized or diffuse hamartomas), kidney (angioleiomyolipoma), breast (breast hamartoma formed by breast lobular fat) and infant liver (mesenchymal hamartoma).

How can hamartoma be cured faster? Actually, this cannot be answered simply, because there are several types of hamartomas, different types have different treatments, and even the same type of hamartomas have different situations. So which method is faster depends on your condition. But no matter what, for your health, you must go to the hospital for treatment in time.

Pulmonary hamartoma: a piece of bronchial tissue inverts and falls off during embryonic development and is surrounded by normal lung tissue. This part of tissue grows slowly or may not grow for a certain period of time, and then gradually develops into a tumor. Most cases occur after the age of 40.

The treatment of lung cancer should also be selected according to the type of lung cancer. For example, radiotherapy is used differently in different cancers. Radiotherapy for small cell lung cancer is often combined with chemotherapy; radiotherapy for non-small cell lung cancer includes preoperative radiotherapy, postoperative radiotherapy, radical radiotherapy, brachytherapy, and interstitial radiotherapy.

Renal Hamartoma: Renal Hamartoma, also known as renal angiomyolipoma, is a benign tumor. Over the years, the incidence has tended to increase, which may be related to the improvement of diagnostic technology. Renal Hamartoma can be an independent disease or accompanied by tuberous sclerosis, the latter of which is autosomal dominant. The clinical features are multiple lesions in both kidneys, combined with mental retardation, butterfly-shaped sebaceous adenoma on the face, etc. It is more common in women, and the age of onset is mostly 20-50 years old. However, the vast majority of patients with renal Hamartoma in my country do not have tuberous sclerosis.

Renal hamartoma can be diagnosed by B-ultrasound and CT scans, which have a high positioning and qualitative diagnosis rate for renal tumors. If the renal hamartoma is smaller than 8 cm, conservative treatment with a combination of Chinese and Western medicine can be used. If the renal hamartoma is larger than 8 cm, surgical treatment should be considered.

Biliary hamartoma: A hamartoma caused by an obstruction in the transformation of the bile duct plate into the bile duct during embryonic development and insufficient absorption. This disease is also known as von Meyenburg syndrome, which is characterized by multiple, uniformly sized cystic lesions surrounded by varying amounts of fibrous matrix. The incidence of biliary hamartoma is about 1% to 3%. It is generally asymptomatic and is discovered accidentally, and does not require special treatment. There have been reports of successful liver transplantation using livers with biliary hamartomas as donor livers. There are literature reports that this disease can cause unclear abdominal pain and malignant transformation.

For single biliary hamartoma, the impact on surrounding liver tissue is small, and the prognosis is good after simple surgical resection, and there is no report of malignant transformation. For diffuse biliary hamartoma, some patients often have repeated liver function abnormalities, and liver transplantation should be recommended. Your liver function is normal at present, and you only need to soften and disperse the nodules for cirrhosis.

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