Is fibroma a genetic disease? Genetic disease refers to a disease caused by changes in genetic material or controlled by pathogenic genes. Many fibroma patients are afraid that the disease will be passed on to their children. So today we will take a look at whether fibroma is a genetic disease: The disease of fibroma is mainly caused by abnormal gene chromosomes, that is, it is affected by one's own factors, and has nothing to do with hereditary factors. This disease is not hereditary, so there is no need to worry, and it should not be passed on to the next generation. Fibroids should be surgically removed early, and the surrounding tissues connected should be removed appropriately. Desmoid tumors should be extensively removed early. Pathological examination should be sent after surgery to rule out malignant conditions. Fibroids are more common under the skin, grow slowly, are generally small, have clear edges, smooth surfaces, and are hard in texture and can be pushed. If mixed with other components, they become fibromyomas, fibroadenomas, fibrolipomas, etc. Fibroids, especially desmoid tumors in the abdominal wall muscles, can become malignant and should be completely removed as soon as possible. As macroscopic lesions, fibroids are usually well circumscribed: 1. Desmoid tumor Most of them are round and hard, with dry cut surface, white or yellowish white, and the fiber bundles can be vaguely seen in cross section and longitudinal section when carefully observed. Desmoid tumors not only have more glial fibers, but also the nuclei of connective tissue cells are mostly spindle-shaped. 2. Soft fibroma The cut surface is spongy, with many blood vessels and often edema. The lymph fluid contained can coagulate into a gelatinous state, with few colloid fibers and loosely arranged cells. The appearance of fibroids on the skin is round or oval, with a good shape. Ulcers and secondary infections may occur on the surface, and they appear homogeneous grayish white. |
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