Glomerulonephritis Lobular

Glomerulonephritis is a group of diseases associated with inflammation and damage to the glomerular capillaries of the kidney and its blood vessels. These diseases are quite common and can have serious consequences. One type of glomerulonephritis is lobular glomerulonephritis.

Glomerulonephritis is a disease that is associated with damage and inflammation of the glomerular apparatus of the kidney. It can be caused by various reasons such as infections, allergies, autoimmune disorders and others. With this disease, inflammatory elements are formed in the glomeruli of the kidneys, which lead to impaired blood filtration and the formation of edema.

The most characteristic symptom of lobular type glomuronephritis is the appearance of swelling on the face, arms and legs. Changes in urine analysis may also be observed - the appearance of red blood cells and protein. The main causes of glomurulonephritis are infections and bacteria, as well as autoimmune processes. Treatment for this disease includes the use of antibiotics, immunosuppressants and other drugs, depending on the cause of the disease.

It is important to understand that glomurlunephritis poses a serious danger to human health. If treatment is not started in time, it can lead to the development of kidney failure and other complications. Therefore, it is very important to consult a doctor promptly when the first symptoms of glomuluronephritis appear.

Glomerulonephritis Lobular syndrome

Glomerulonephritis (GN), first described by Francis Gallwey in 1873, is a heterogeneous group of diseases characterized by immune-mediated infiltration of the renal glomeruli by monoclonal cells, predominantly plasma cells and polymorphonuclear cells. The severity of GN can range from a mild increase in protein levels in the urine to acute renal failure. They can have different etiologies and pathogenesis. The study of clinical and morphological features determines the approach to the diagnosis and differential diagnosis of GN. Differential diagnosis is based on the use of a wide arsenal of available morphological, immunohistochemical and molecular biological methods [4]. Throughout the history of glomerulonephytes, two main variants have been classified by origin: primary, an independent condition without an obvious cause, and secondary, as a manifestation of another disease of the hematopoietic and blood organs.