Diffuse infantile fibromatosis

Introduction to diffuse infant fibromatosis Diffuse infantile fibromatosis occurs in children 3 years of age. The damage usually occurs in the upper arm, neck and scapula, and is infiltrated by multiple myocardial fibers and fibroblasts, similar to those seen in sarcolemma. Fibroma is a benign tumor derived from fibrous connective tissue. It has different types due to the different components of fibroids. Because fibrous connective tissue is widely distributed in the human body and constitutes a gap between organs, fibroids can occur in Any part of the body. Among them, skin and subcutaneous tissues are most common, and sarcolemma, periosteum, nasopharyngeal cavity and other mucosal tissues and other organs such as breast, ovary, and kidney can occur. They vary in size and grow slowly. basic knowledge The proportion of illness: the incidence rate is about 0.0003% - 0.0004% Susceptible population: children who occur within 3 years of age Mode of infection: non-infectious complication:

The cause of diffuse infantile fibromatosis

The pathogenesis is still unclear.

Diffuse infant fibromatosis prevention

There is no effective preventive measure for this disease. Early detection and early diagnosis are the key to the prevention and treatment of this disease.

Diffuse infantile fibromatosis complications Complication

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Diffuse infant fibromatosis symptoms Common symptoms Facial angiofibroma

The damage usually occurs in the upper arm, neck and scapula, and is infiltrated by multiple myocardial fibers and fibroblasts. Similar to sarcoplasmic fibroids, no calcification occurs, and 1/3 of patients can relapse after surgical resection.

According to clinical manifestations, the characteristics of skin lesions can be diagnosed.

Examination of diffuse infant fibromatosis

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Diagnosis and diagnosis of diffuse infant fibromatosis

According to clinical manifestations, the characteristics of skin lesions can be diagnosed.

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