lymphoblastic lymphosarcoma - translation to ρωσικά
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lymphoblastic lymphosarcoma - translation to ρωσικά

LEUKEMIA THAT IS CHARACTERIZED BY OVER PRODUCTION OF LYMPHOBLASTS.
Acute lymphoblastic leukaemia; Acute lymphocytic leukaemia; Acute lymphocytic leukemia; Acute Lymphoblastic Leukemia; Leukemia, lymphocytic, acute; Lymphoblastic lymphoma; Lymphoblastic Lymphoma; Leukemia, lymphoblastic, acute; Acute b-cell leukemia; All-l1; Acute lymphoid leukemia; B-cell acute lymphoblastic leukemia; B-ALL; Lymphoblastic leukemia
  • In ALL, lymphoid cell development stops at the lymphoblast (arrow), which are also overproduced.
  • Graphs of overall survival rates at 5 years and 10 years in people in pediatric care and adults with ALL
  • intravenous access]] for [[chemotherapy]]

lymphoblastic lymphosarcoma      

медицина

лимфобластическая (лимфобластная) лимфосаркома

lymphoblastic         
CELL TYPE
Lymphoblastic; Lymphoma, lymphoblastic; Lymphoblasts; CFU-L; Lymphoid progenitor cell; Lymphoblastoid

медицина

лимфобластный

lymphoblast         
CELL TYPE
Lymphoblastic; Lymphoma, lymphoblastic; Lymphoblasts; CFU-L; Lymphoid progenitor cell; Lymphoblastoid

общая лексика

лимфобласт

Ορισμός

lymphoblast
['l?mf?(?)blast]
¦ noun Medicine an abnormal cell resembling a large lymphocyte, produced in large numbers in a form of leukaemia.
Derivatives
lymphoblastic adjective

Βικιπαίδεια

Acute lymphoblastic leukemia

Acute lymphoblastic leukemia (ALL) is a cancer of the lymphoid line of blood cells characterized by the development of large numbers of immature lymphocytes. Symptoms may include feeling tired, pale skin color, fever, easy bleeding or bruising, enlarged lymph nodes, or bone pain. As an acute leukemia, ALL progresses rapidly and is typically fatal within weeks or months if left untreated.

In most cases, the cause is unknown. Genetic risk factors may include Down syndrome, Li–Fraumeni syndrome, or neurofibromatosis type 1. Environmental risk factors may include significant radiation exposure or prior chemotherapy. Evidence regarding electromagnetic fields or pesticides is unclear. Some hypothesize that an abnormal immune response to a common infection may be a trigger. The underlying mechanism involves multiple genetic mutations that results in rapid cell division. The excessive immature lymphocytes in the bone marrow interfere with the production of new red blood cells, white blood cells, and platelets. Diagnosis is typically based on blood tests and bone marrow examination.

ALL is typically treated initially with chemotherapy aimed at bringing about remission. This is then followed by further chemotherapy typically over a number of years. Treatment usually also includes intrathecal chemotherapy since systemic chemotherapy can have limited penetration into the central nervous system and the central nervous system is a common site for relapse of acute lymphoblastic leukemia.

Treatment can also include radiation therapy if spread to the brain has occurred. Stem cell transplantation may be used if the disease recurs following standard treatment. Additional treatments such as Chimeric antigen receptor T cell immunotherapy are being used and further studied.

ALL affected about 876,000 people globally in 2015 and resulted in about 111,000 deaths. It occurs most commonly in children, particularly those between the ages of two and five. In the United States it is the most common cause of cancer and death from cancer among children. ALL is notable for being the first disseminated cancer to be cured. Survival for children increased from under 10% in the 1960s to 90% in 2015. Survival rates remain lower for babies (50%) and adults (35%).

Μετάφραση του &#39lymphoblastic lymphosarcoma&#39 σε Ρωσικά