Lymphosarcomatosis [Lymphosar Comatosis; Lymphosarcoma (Basic Lymphosarcoma-) + -Oz; You are Kundrata Disease]

What is lymphosarcomatosis? Lymphosarcomatosis is a rather rare and difficult to treat disease (lymphasarcomatous syndrome), which is manifested by multiple pathologies of lymphoid tissue. Often found in children and the elderly. It is not considered to be oncological in nature, but there is a high probability of its transformation into a tumor. It is found in most developed countries - on the European continent 13 times more often than in the USA, Canada and Australia. It is most common among residents of Japan, China and India. Most often occurs in middle-aged men (45–65 years). During the course of the disease, it affects both the lymph nodes and the bone marrow - this is a very dangerous condition for humans. In this regard, doctors prevent this disease by offering vaccination against lymphosarcomatosis to kindergarten and schoolchildren. Lymphosarcoma is still considered incurable.

Kundrat's lymphadenopathy

(Kudra's lymphadenitis) is a systemic oncological disease in which tissues are affected by slowly growing malignant lymphocytes. They are most often caused by the Epstein-Barr virus (VHHV-4). This disorder is also known by various names such as Hand's disease, herpesvirus lymphoma, generalized lymphonodular sarcomatoidosis, or Kundra's lymphovasculorrhagia. It also includes damage to the lymph glands and other organs. It is characterized by enlargement, redness and even pain in the lymph nodes