Intravenous immunoglobulin-induced thrombocytopenia: a case report and review of the literature (notice n° 159945)
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fixed length control field | 02348cam a2200301 4500500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250112032506.0 |
041 ## - LANGUAGE CODE | |
Language code of text/sound track or separate title | fre |
042 ## - AUTHENTICATION CODE | |
Authentication code | dc |
100 10 - MAIN ENTRY--PERSONAL NAME | |
Personal name | Fukuzono, Maki |
Relator term | author |
245 00 - TITLE STATEMENT | |
Title | Intravenous immunoglobulin-induced thrombocytopenia: a case report and review of the literature |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Date of publication, distribution, etc. | 2023.<br/> |
500 ## - GENERAL NOTE | |
General note | 10 |
520 ## - SUMMARY, ETC. | |
Summary, etc. | Background. Intravenous immunoglobulin (IVIG), a pooled blood product acquired from multiple healthy donors, is an effective treatment for various types of autoimmune diseases, haematological disorders, and infectious diseases. Adverse haematological events such as throm-bocytopenia are rarely caused by IVIG. Objectives. To investigate the phenomenon of IVIG-induced thrombocytopenia. Materials & Methods. A case study and a review of the previous literature based on a search using MEDLINE (PubMed) and ICHUSHI (for Japanese literature) electronic databases. Results. The present case of dermatomyositis exhibited two episodes of IVIG-induced thrombocytopenia, which occurred a few days after initiating IVIG and was significant within two weeks without haemorrhagic symptoms. Spontaneous remission of thrombocytopenia was repeatedly observed. Based on a review of five cases, the underlying disorders were autoimmune bullous diseases in three of the five cases. Polyethylene glycol-treated human immunoglobulin products were used in three of the five cases. The clinical course of IVIG-induced thrombocytopenia was similar to that in our present case. Conclusion. Because of the rarity of severe haemorrhagic symptoms and spontaneous remission of IVIG-induced thrombocytopenia, discontinuation of IVIG due to thrombocytopenia is not straightforward. |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
Topical term or geographic name as entry element | thrombocytopenia |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
Topical term or geographic name as entry element | adverse event |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
Topical term or geographic name as entry element | intravenous immunoglobulin |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
Topical term or geographic name as entry element | thrombocytopenia |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
Topical term or geographic name as entry element | adverse event |
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
Topical term or geographic name as entry element | intravenous immunoglobulin |
700 10 - ADDED ENTRY--PERSONAL NAME | |
Personal name | Okiyama, Naoko |
Relator term | author |
700 10 - ADDED ENTRY--PERSONAL NAME | |
Personal name | Iwasaki, Riko |
Relator term | author |
700 10 - ADDED ENTRY--PERSONAL NAME | |
Personal name | Endo, Ruriko |
Relator term | author |
700 10 - ADDED ENTRY--PERSONAL NAME | |
Personal name | Sasaki, Katsuhito |
Relator term | author |
700 10 - ADDED ENTRY--PERSONAL NAME | |
Personal name | Inoue, Sae |
Relator term | author |
700 10 - ADDED ENTRY--PERSONAL NAME | |
Personal name | Nomura, Toshifumi |
Relator term | author |
786 0# - DATA SOURCE ENTRY | |
Note | European Journal of Dermatology | 21 | 3 | 2023-09-26 | p. 373-376 | 1167-1122 |
856 41 - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="https://shs.cairn.info/journal-european-journal-of-dermatology-2022-3-page-373?lang=en">https://shs.cairn.info/journal-european-journal-of-dermatology-2022-3-page-373?lang=en</a> |
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