How is skin dysplasia treated?

summary

Dysplasia of skin, also known as congenital skin defect, is a congenital defect of epidermis and dermis in one or several areas, sometimes even subcutaneous tissue. How is skin dysplasia treated? Then follow me to understand the treatment and nursing of this disease.

How is skin dysplasia treated?

At birth, there is a well-defined skin defect with rough base and red granuloma, which is manifested as a large thick walled bulla. The top of the bulla falls off quickly, and the scalp defect is about 60%. It is usually 2cm, which can be as large as 9cm, and it can also be long, triangular or star shaped. The healing of the defect wound is slow, and it can scab repeatedly and fall off for months or even years. It may be accompanied by other developmental abnormalities, such as congenital amputation, and most patients are accompanied with epidermolysis bullosa.

The healing of the defect wound is slow, and it can scab repeatedly and fall off for months or even years. It may be accompanied by other developmental abnormalities, such as congenital amputation, and most patients are accompanied with epidermolysis bullosa. The pathogenesis is still unclear. It may be related to primary differentiation defect and adjacent amniotic membrane development defect.

It is autosomal dominant or recessive inheritance. It may also be related to primary differentiation defect and adjacent amniotic membrane development defect. Skin dysplasia is a congenital defect in one or several areas of epidermis and dermis, sometimes even in subcutaneous tissue. Sometimes it can be confused with forceps trauma, but it can be diagnosed from its shape, location and clear penetrating edge. Epidermal nevus should also be differentiated.

matters needing attention

Attention should be paid to nursing care in infancy to control secondary infection, which can be corrected by plastic surgery later. It may be accompanied by other developmental abnormalities, such as congenital amputation, and most patients are accompanied with epidermolysis bullosa. It is autosomal dominant or recessive inheritance. It may also be related to primary differentiation defect and adjacent amniotic membrane development defect.