WordNet
- any of several blood diseases causing subcutaneous bleeding (同)peliosis
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English Journal
- A bead-based assay in the work-up of suspected platelet alloimmunization.
- Cooper N1, Bein G1,2, Heidinger K1, Santoso S1, Sachs UJ1,2.
- Transfusion.Transfusion.2015 Nov 6. doi: 10.1111/trf.13351. [Epub ahead of print]
- BACKGROUND: Alloantibodies against human platelet antigens (HPAs) are of clinical significance in immune-mediated thrombocytopenia such as fetal/neonatal alloimmune thrombocytopenia (FNAIT), posttransfusion purpura, and platelet (PLT) transfusion refractoriness. The gold standard for the detection o
- PMID 26545411
- Sulfamethoxazole-induced thrombocytopenia masquerading as posttransfusion purpura: a case report.
- Nixon CP1, Cheves TA2, Sweeney JD2.
- Transfusion.Transfusion.2015 Nov;55(11):2738-41. doi: 10.1111/trf.13197. Epub 2015 Jun 22.
- BACKGROUND: Drug-induced immune thrombocytopenia (DITP) is a rare clinical disorder characterized by accelerated platelet (PLT) clearance in the presence of drug-dependent antibodies. Distinguishing DITP from other immune-mediated disorders such as posttransfusion purpura (PTP) and autoimmune thromb
- PMID 26098194
- Shedding a little light on posttransfusion purpura.
- Roubinian NH1, Leavitt AD.
- Transfusion.Transfusion.2015 Feb;55(2):232-4. doi: 10.1111/trf.12934.
- PMID 25683186
Japanese Journal
- I型CD36欠損症を合併した虚血性心疾患患者に対する無輸血開心術
- 奥村 悟,大川原 潤,前田 吉宣
- 日本心臓血管外科学会雑誌 32(5), 297-299, 2003-09-15
- I型CD36欠損症患者では,妊娠や輸血によりCD36(Nak^a)に感作されることで抗CD36抗体(anti-Nak^a)を産生し,その後の輸血にさいし血小板輸血不応答や輸血後紫斑病を惹起する.症例は72歳,女性.妊娠歴,輸血歴ともになし.65歳時より高血圧症と心不全に対し内科的加療を受けてきた.この間,^<123>I-β-methyl-iodophenyl pentadecanoic …
- NAID 110003992871
- Posttransfusion purpura-like syndrome associated with CD 36 (Nak^a) isoimmunization
Related Links
- posttransfusion purpura Transfusion medicine A nonimmune response to transfusion of packed RBCs and FFP, attributed to passive transfer of antibodies from donor plasma, resulting in complement activation and lung injury Clinical ...
- Thirteen cases of posttransfusion purpura (PTP) which were diagnosed in Germany and Austria from 1977–1985 are described. All patients were women with a mean age of 58.6 years (range, 36–77 years). Al
★リンクテーブル★
[★]
- 英
- posttransfusion purpura, post-transfusion purpura
- 同
- シュルマン症候群 Shulman syndrome
- 関
- 輸血後合併症
- Sabiston Textbook of Surgery, 18th ed.
- Table 6-4 -- Categories and Management of Adverse Transfusion Reactions
Delayed (>24 Hours) Transfusion Reactions?Immunologic
|
TYPE
|
INCIDENCE
|
ETIOLOGY
|
MANIFESTATION
|
DIAGNOSTIC TESTING
|
THERAPEUTIC/PROPHYLACTIC APPROACH
|
Post-transfusion purpura
|
Rare
|
Recipient platelet antibodies (apparent alloantibody, usually anti? HPA-1) destroy autologous platelets
|
Thrombocytopenic purpura, bleeding 8-10 days after transfusion
|
Platelet antibody screen and identification
|
IGIV|HPA-1?negative platelets|Plasmapheresis
|
[★]
- 関
- posttransfusional
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