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IDIOPATHIC THROMBOCYTOPENIC PURPURA

Main Authors: ., Alvina, Aulia, Diana
Format: Article info eJournal
Bahasa: ind
Terbitan: PERHIMPUNAN DOKTER SPESIALIS PATOLOGI KLINIK INDONESIA , 2018
Subjects:
thrombocytopenia
thrombocyte autoantibody
Online Access: http://www.indonesianjournalofclinicalpathology.or.id/index.php/patologi/article/view/1036
ctrlnum article-1036
fullrecord <?xml version="1.0"?> <dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><title lang="en-US">IDIOPATHIC THROMBOCYTOPENIC PURPURA</title><creator>., Alvina</creator><creator>Aulia, Diana</creator><subject lang="en-US">thrombocytopenia, thrombocyte autoantibody</subject><description lang="en-US">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. Idiopathicthrombocytopenic purpura is classified as primary or secondary. The primary ITP is classified as acute and chronic.. Children and adultonset 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 idiopathicthrombocytopenic purpura remains one of exclusion after other thrombocytopenic disease are ruled out based on history and needanamnesa, physical examination, thrombocyte count, perifer blood smear examination, bone marrow smear examination. The treatmentis to raise the platelet count into a hemostatically safe range. This article presented a study case of idiopathic thrombocytopenic purpuraon an old woman with DIC which caused her death.</description><publisher lang="en-US">PERHIMPUNAN DOKTER SPESIALIS PATOLOGI KLINIK INDONESIA</publisher><contributor lang="en-US"/><date>2018-03-17</date><type>Journal:Article</type><type>Other:info:eu-repo/semantics/publishedVersion</type><type>Journal:Article</type><identifier>http://www.indonesianjournalofclinicalpathology.or.id/index.php/patologi/article/view/1036</identifier><identifier>10.24293/ijcpml.v16i3.1036</identifier><source lang="en-US">INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY; Vol 16, No 3 (2010); 149-151</source><source>2477-4685</source><source>0854-4263</source><source>10.24293/ijcpml.v16i3</source><language>ind</language><rights lang="en-US">Copyright (c) 2018 INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY</rights><rights lang="en-US">http://creativecommons.org/licenses/by-nc-nd/4.0</rights><recordID>article-1036</recordID></dc>
language ind
format Journal:Article
Journal
Other:info:eu-repo/semantics/publishedVersion
Other
Journal:eJournal
author ., Alvina
Aulia, Diana
title IDIOPATHIC THROMBOCYTOPENIC PURPURA
publisher PERHIMPUNAN DOKTER SPESIALIS PATOLOGI KLINIK INDONESIA
publishDate 2018
topic thrombocytopenia
thrombocyte autoantibody
url http://www.indonesianjournalofclinicalpathology.or.id/index.php/patologi/article/view/1036
contents 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. Idiopathicthrombocytopenic purpura is classified as primary or secondary. The primary ITP is classified as acute and chronic.. Children and adultonset 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 idiopathicthrombocytopenic purpura remains one of exclusion after other thrombocytopenic disease are ruled out based on history and needanamnesa, physical examination, thrombocyte count, perifer blood smear examination, bone marrow smear examination. The treatmentis to raise the platelet count into a hemostatically safe range. This article presented a study case of idiopathic thrombocytopenic purpuraon an old woman with DIC which caused her death.
id IOS5364.article-1036
institution Indonesian Journal of Clinical Pathology and Medical Laboratory (IJCP & ML)
institution_id 1807
institution_type library:special
library
library Indonesian Journal of Clinical Pathology and Medical Laboratory
library_id 1493
collection Indonesian Journal of Clinical Pathology and Medical Laboratory (IJCP & ML)
repository_id 5364
subject_area Patologi Klinik
city KOTA SURABAYA
province JAWA TIMUR
repoId IOS5364
first_indexed 2018-04-01T07:52:47Z
last_indexed 2018-04-01T07:53:18Z
recordtype dc
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