Talk about the most detailed introduction of fibroids

In recent years, due to the improvement of living standards, fibroids are also a very common disease in life. However, the human body is relatively weak, which is also a problem for everyone. There are many reasons for fibroids. Let's learn about the most detailed introduction of fibroids.

According to the age and location of onset, the main types of tumors include juvenile fibromatosis, cervical fibromatosis, infantile fibromatosis, infantile myofibromatosis, and lipofibromatosis. The age of onset is mostly between 30 and 50 years old, and it is also common in children and adolescents. Tumors can occur in large muscles anywhere in the body, with the rectus abdominis and the aponeurosis of the adjacent muscles of the abdominal wall being the most common, and are more common during pregnancy and late pregnancy. Those outside the abdominal wall are more common in men, and are more common in the scapula, thigh, and buttocks.

Clinical manifestations are divided into the following categories according to the age of onset and the affected parts:

1. Juvenile fibromatosis occurs in children and young people.

2. Cervical fibromatosis refers to a type of fibromatosis that manifests at birth or shortly after birth and involves the lower 1/3 of the sternocleidomastoid muscle, sometimes bilaterally. Cervical fibromatosis is often accompanied by various congenital abnormalities.

3. Infant and young children's digital fibromatosis is a type of fibromatosis that usually occurs only in childhood. It typically occurs on the outer side of the finger (toe) tip, but can also occur in other parts of the body, such as the mouth and breast. This disease is often multiple and usually occurs at birth or within 2 years of age.

4. Infantile myofibromatosis is a solitary or multiple nodular lesion that occurs in the skin, soft tissue or bone. It can be confined to the above-mentioned parts or accompanied by the involvement of internal organs. The disease mostly occurs before the age of 2, and about 60% is congenital. The disease can also be seen in adults, with solitary cases more common in males and multiple cases more common in females. Familial cases are known, and evidence of autosomal dominant inheritance has been found.

5. Lipofibromatosis is a subtype of infantile fibromatosis, and local recurrence is common.

6. Multiple hyaline fibromatosis is a morphologically specific, familial multiple fibromatosis affecting children. It has no symptoms at birth and may be caused by congenital metabolic abnormalities.

7. Other cases include penile fibromatosis, palmar fibromatosis, plantar fibromatosis, scar fibromatosis and post-irradiation fibromatosis. Fibromatosis associated with multiple colon polyposis and occasionally multiple osteomas is called Gardner syndrome.