What is the chance of fibroids being inherited?

What is the probability of fibroids being inherited? While fibroid patients are suffering from the disease and psychological burden, they also have to face other effects brought by the fibroid disease, that is, whether they can get married and have children. So today I will introduce to you, what is the probability of fibroids being inherited?

The chance of inheritance is very small. Similar inherited diseases will only occur when people have similar living habits. For example, if they like to eat the same food, are petty and sulky, and when the person's stomach and gallbladder are not in good condition, and when the positive energy cycle is weak, sulking will cause blockage of the gallbladder and stomach meridians in the breast, forming fibroids. If you pay attention to adjusting the function of your internal organs and your mood, you will not get fibroids.

Fibromas are composed of well-differentiated subcutaneous connective tissue. They are common in adults aged 40-50 years old. They are often found under the skin and grow slowly. They are usually small, with clear edges, smooth surface, hard texture, and can be pushed. If mixed with other components, they become fibromyoma, fibroadenoma, fibrolipoma, etc. According to the age and location of onset, they mainly include juvenile fibromatosis, cervical fibromatosis, infantile fibromatosis, infantile myofibromatosis, lipofibromatosis, etc.

There are several types of fibroma: Yellow fibroma is prone to occur in the dermis or subcutaneous layer of the trunk and proximal upper arm. It often arises from small papules after trauma or itching. The lumps are hard with unclear edges. Because they are accompanied by internal bleeding, they contain hemosiderin and are dark brown. If the tumor is larger than 1 cm and grows rapidly, it should be suspected to be fibrosarcoma and must be completely removed surgically.

Fibroids grow slowly and generally stop growing when they develop to a certain size. They are benign tumors composed of well-differentiated subcutaneous connective tissue and rarely become malignant. Surgical resection is the main treatment.