Publication:
Severe Immune Thrombocytopenic Purpura Treated with Plasma Exchange

creativeworkseries.issn1812-2027
dc.contributor.authorSigdel, M R
dc.contributor.authorShah, D S
dc.contributor.authorKafle, M P
dc.contributor.authorRaut, K B
dc.date.accessioned2025-08-21T07:42:32Z
dc.date.available2025-08-21T07:42:32Z
dc.date.issued2012
dc.descriptionSigdel M R, Shah D S, Kafle M P, Raut K B Department of Internal Medicine, TU Teaching Hospital, Kathmandu, Nepal.
dc.description.abstractABSTRACT Immune thrombocytopenic purpura (ITP) is a hematological disorder characterized by immunologically mediated destruction of platelets and absence of other causes of thrombocytopenia. Treatment is required when the low platelet count entails risk of serious bleeding. Steroid is the first line of management. Acute refractory ITP with very low platelet count is variably treated with high dose steroid, intravenous immunoglobulin (IVIg), anti D or emergency splenectomy. Here, we present a case of steroid resistant ITP with severe thrombocytopenia treated with plasma exchange and low dose IVIg who responded dramatically to the therapy with maintained platelet count till one month from the institution of therapy. KEY WORDS immune thrombocytopenic purpura, intravenous immunoglobulin, plasma exchange
dc.identifier.urihttps://hdl.handle.net/20.500.14572/1887
dc.language.isoen_US
dc.publisherKathmandu University
dc.titleSevere Immune Thrombocytopenic Purpura Treated with Plasma Exchange
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage87
oaire.citation.startPage85
relation.isJournalIssueOfPublicationd42baeb4-edc7-4097-b102-62aad3c78671
relation.isJournalIssueOfPublication.latestForDiscoveryd42baeb4-edc7-4097-b102-62aad3c78671
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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