期刊名称：International Journal of Early Childhood Special Education
电子版ISSN：1308-5581
出版年度：2022
卷号：14
期号：4
页码：2179-2182
DOI：10.9756/INTJECSE/V14I4.277
语种：English
出版社：International Journal of Early Childhood Special Education
摘要：Introduction : When the immune system incorrectly attacks platelets, idiopathic thrombocytopenic purpura (ITP) might develop. It can also develop after viral infection in youngsters; it may be persistent in adulthood. Platelets are blood cells that assist in the clotting process. Easy bruising, bleeding gums, and internal bleeding can all be symptoms of a low platelet count. Main symptoms and clinical findings: A female 35 years old was admitted to AVBRH with chief complaints of prolonged heavy bleeding, Reddish-purple patches on the lower legs, some as small as a pinhead, weakness, lethargy, itching fever and abdominal pain. Main diagnosis, therapeutic interventions, and outcomes: A 35 years old femalewas admitted to Tertiary Care hospital with chief complaints of prolonged heavy bleeding, Reddish-purple patches on the lower legs, some as small as a pinhead, weakness, lethargy and fever, and abdominal pain. She came for treatment, and her treatment started at the time of injectable admission pan of 40 mg, antiemetics, I. V fluid DNS, D5 began to. Advised to check vital signs and maintain records and observation of spots on the skin.Blood test; Hb 10.6% , MCV 62.5%,MCH 19.6%Total RBC 5.38,Total WBC 5700,Total platelet count 40,000Monocytes 05,Granulocytes 80,Lymphocytes 14.Inj. ceftriaxone 500 mg BD, inj. Pan 40 mg, BD, inj. Romiplostim started.As far as the patient treatment is ongoing and the patient prognosis is better Conclusion : Idiopathic thrombocytopenic purpura is a rare condition primarily in children found in adults age and uncommon in youngsters. Patient with HIV infection, hepatitis and viral infection has more likely to get this illness. In this case, the patient is stable and got the proper treatment overall, and his condition is better than at the time of admission.
关键词：idiopathic thrombocytopenic purpura;platelet;immune system
