Pseudosclerodermiformis symmetrical chronic granulomatosis (G. pseudosclerodermiformis symmetrica chronica) is a rare chronic disease characterized by the formation of granulomas and symmetrical skin lesions. This condition is also known by other names such as symmetrical chronic granulomatosis and symmetrical granulomatosis.
The reasons for the development of pseudosclerodermiform symmetrical chronic granulomatosis are not fully understood. However, it is believed that immunological disorders and genetic factors may play a role in its occurrence. The chronic nature of the disease means that it usually lasts a long time, and symmetrical skin lesions are characterized by skin changes appearing on both sides of the body at the same time.
Symptoms of pseudosclerodermiformis chronic granulomatosis include the formation of granulomas, which are inflammatory tumors typically ranging in size from a few millimeters to several centimeters. These granulomas can occur on various areas of the skin, including the face, extremities, trunk, and mucous membranes. They can be painful and itchy.
Other characteristics of this disease include thickening and hardening of the skin, similar to scleroderma symptoms, and possible damage to internal organs such as the lungs, heart, or kidneys. However, internal organ involvement is rare and not always present.
The diagnosis of pseudosclerodermiformis symmetrical chronic granulomatosis can be difficult because its symptoms may resemble other diseases such as scleroderma or sarcoidosis. A skin biopsy, blood tests, and imaging of internal organs may be required to make an accurate diagnosis.
Treatment of pseudosclerodermiformis symmetrical chronic granulomatosis is aimed at alleviating symptoms and controlling inflammation. Doctors may prescribe anti-inflammatory medications, such as nectatin or corticosteroids, to reduce inflammation and pain. In addition, immunosuppressants may be used to suppress the activity of the immune system.
Although pseudosclerodermiform symmetrical chronic granulomatosis is a rare disease, its diagnosis and treatment require a careful approach and consultation with specialists such as rheumatologists, dermatologists and immunologists.
In conclusion, granulomatosis pseudosclerodermiformis symmetrical chronic is a complex and rare disease characterized by the formation of granulomas and symmetrical skin lesions. Its exact causes and mechanisms of development are still not fully understood. To establish a diagnosis and prescribe appropriate treatment, consultation with experienced specialists is necessary. Early detection and timely treatment can help alleviate symptoms and improve the quality of life for patients suffering from this rare disease.