How do you get intrarenal hamartoma

Renal hamartoma is a congenital disorder in which certain tissues appear in places where they should not be during embryonic development, such as hair, bones, and even teeth. Once you have a renal hamartoma, you need active treatment to eliminate symptoms such as hydronephrosis, dysuria, and low back pain.

Renal hamartoma is a type of renal angiomyolipoma, which is formed by abnormal proliferation of vascular smooth muscle and adipose tissue to varying degrees. It can occur in the kidneys, brain, heart, eyes, lungs, bones and other parts. In recent years, with the development of medical technology, many diseases have been improved, but before treating any disease, it is necessary to understand the cause clearly. Let's learn about it below.

First, intrarenal hamartoma is also called angiomyolipoma. The cause is still unclear. Foreign reports show that it is related to heredity, mainly related to tuberous sclerosis. This disease is relatively rare in my country and usually occurs alone. Sometimes, in addition to the kidney, it also exists in the lungs, liver, eyes, brain and other parts.

Second, 80% of the patients with renal hamartoma are women. Generally, when the tumor is small, the patient has no clinical symptoms. Later, as the volume increases, it may affect the digestive system, and the cause of this disease is related to intratumoral bleeding. Moreover, angiomyolipoma is a common tumor rupture disease, which can cause hemorrhagic shock. After the disease is diagnosed, it is recommended to improve the disease through interventional embolization or nephrectomy.

Third, intrarenal hamartoma is a tumor composed of different components and contents of blood vessels, smooth muscle tissue and fat tissue. It is generally not cancer, but benign. In most cases, it is more common in women than in men, and may also be secondary to tuberous sclerosis, i.e. tuberous sclerosis. When the tumor grows to a certain extent or complications occur, it is recommended to receive treatment as soon as possible, such as surgical treatment, which can remove the tumor and eliminate the harmfulness of the disease.

Renal hamartoma is a congenital disease, that is, during the development process, strain tissue proliferates in a position where it should not exist. This is related to genes, but there is no clear mechanism yet. It is generally related to family inheritance and gene defects. Under normal circumstances, single renal hamartoma should be discovered and treated early, so as to eliminate the harm of the disease and ensure that the disease can be completely cured.