IDIOPATHIC THROMBOCYTOPENIC PURPURA  

Oleh:

Alvina ; Aulia, Diana

Jenis: Article from Journal - ilmiah nasional - terakreditasi DIKTI
Dalam koleksi: Indonesian Journal of Clinical Pathology and Medical Laboratory vol. 16 no. 3 (Jul. 2010), page 149-151.
Topik: thrombocytopenia; thrombocyte autoantibody

Ketersediaan

Perpustakaan FK Nomor Panggil: I01.K Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

Lihat Detail Induk

Isi artikel

Idiopathic thrombocytopenic purpura is an autoimunne disease with low platelet count and bleeding manifestation like purpura, echymosis, petechie, mucosa membrane bleeding. The cause of ITP is platelet coated with specific thrombocyte autoantibody. idiopathic thrombocytopenic purpura is classified as primary or secondary. The primary ITP is classified as acute and chronic .. Children and adult onset idiopathic thrombocytopenic purpura are different. An Acute ITP can be found in children and chronic onset can be found in adult. The duration of bleeding may help to distinguish acute and chronic idiopathic thrombocytopenic purpura. The diagnosis of idiopathic thrombocytopenic purpura remains one of exclusion after other thrombocytopenic disease are ruled out based on. history and need anamnesa. Physical examination, thrombocyte count, perifer blood smear examination, bone marrow. smear examination. The treatment is to raise the platelet count into a hemostatically safe range. This article presented a study case of idiopathic thrombocytopenic purpura on an old woman with DIC which caused her death.

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