PPT-Immune thrombocytopenic purpura (ITP)

Ali Al Khader MD Faculty of Medicine AlBalqa Applied University Email alialkhaderbauedujo ITP 2 clinical subtypes 1Chronicrelatively common women between 20 amp 40. Abstract. Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura is thought to be due to autoimmune disease. An abnormal autoantibody (immunoglobulin G) binds to the platelet membrane, causing removal by the spleen. If left untreated it could lead to bleeding and possibly death (. Immune. System. Factors of Immune Health. A number of factors contribute to immune health. Exercise. Feelings of stress. Nutrition. Essential oils*. *These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.. Ophthalmic manifestation of congenital protein C deficiency Dr Shahla ansary peiatric heamatologyonclogist Dr Amir hesabi Assistant pediatric hematologyoncologist Case 1 CC: purpura fulminans By: Dr. Donna Braham. Objectives. Classify Vasculitis. Know when to consider Vasculitis. Rule out mimickers of Vasculitis. Diagnose cutaneous small vessel vasculitis – In . particular Henoch–. Schönlein. Curtis Barry, MD. UMASS ECHO. April 28, 2017. Disclosure. I have no financial disclosures related to this subject. Background. HCV primarily affects the liver but other organ systems can become involved. HIV. (Human immunodeficiency virus)- a virus that attacks the immune system.. Infection with HIV can be prevented. Responsible decisions is the most valuable tool for protection against HIV.. Example: Abstinence from sexual activity and injecting drugs reduce your risk.. in a young girl. Dr.Manoj. . Prakash.J. JR-II. Dept. of Medicine. HISTORY. A 16 Yrs old female patient came to . casulty. . c/o . massive Per vaginal bleeding since 15 days. . She also complained of giddiness and breathlessness on . ARC Jour Volume 4 , Issue 2, 2019, PP 1 - 4 www.arcjournals.org ARC Journal of Hematology Page | 1 Difficulties Diagnostic of Amegacaryocytic Thrombocytopenic Purpura in Developing Country: A Case increased with age. In another prospective cohort analysis of newly presenting adults withplatelet counts less than 50,000/ cu mm in the Northern HealthRegion of the United Kingdom, the female-male ra 32 Childhood Immune Thrombocytopenia: Long-term Follow-up Data Evaluated by the Criteria of the International Working Group on Immune Immune thrombocytopenia (ITP) is a common bleeding disorder in c 1 Corresponding AuthorNoël GStrasbourg University, CNRS, IPHC, UMR 7178, Institute of Cancerology Strasbourg Europe (ICANS), UNICANCER, Paul Strauss Comprehensive Cancer Center, Radiobiology Laborat clastic. vasculitis. . The . majority of cases occur as sequelae to strangles. However, Cases also occur following. . immunization against . S. . equi. . and as sequelae to infection with other streptococci.. . jithin. P JR1 Medicine. introduction. P. latelets. are one of the blood cells that are released from megakaryocytes. Thrombocytopenic Thrombotic Purpura (TTP). Clinical manifestations (<10% have pentad):. Microangiopathic. hemolytic anemia (MAHA). Thrombocytopenia. Fever. Renal insufficiency . Neurological symptoms.