薬剤性自己免疫性溶血性貧血
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2019/06/17 15:20:58」(JST)
[Wiki en表示]
Drug-induced autoimmune heamolytic anemia |
---|
Specialty | Hematology |
---|
Drug-induced autoimmune hemolytic anemia is a form of hemolytic anemia.
In some cases, a drug can cause the immune system to mistakenly think the body's own red blood cells are dangerous, foreign substances. Antibodies then develop against the red blood cells. The antibodies attach to red blood cells and cause them to break down too early. Drugs that can cause this type of hemolytic anemia include:
- Cephalosporins (a class of antibiotics) – most common cause[citation needed]
- Dapsone
- Levodopa
- Levofloxacin
- Methyldopa
- Nitrofurantoin
- Nonsteroidal anti-inflammatory drugs (NSAIDs)
- Phenazopyridine (pyridium)
- Quinidine[1]
Penicillin in high doses can induce immune mediated hemolysis[2] via the hapten mechanism in which antibodies are targeted against the combination of penicillin in association with red blood cells. Complement is activated by the attached antibody leading to the removal of red blood cells by the spleen.[citation needed]
The drug itself can be targeted by the immune system, e.g. by IgE in a Type I hypersensitivity reaction to penicillin, rarely leading to anaphylaxis.[citation needed]
See also
- List of circulatory system conditions
- List of hematologic conditions
References
- ^ MedlinePlus Encyclopedia Drug-induced immune hemolytic anemia
- ^ Stroncek, David; Procter, Jo L.; Johnson, Judy (2000). "Drug-induced hemolysis: Cefotetan-dependent hemolytic anemia mimicking an acute intravascular immune transfusion reaction". American Journal of Hematology. 64 (1): 67–70. doi:10.1002/(SICI)1096-8652(200005)64:1<67::AID-AJH12>3.0.CO;2-Z. PMID 10815791.
External links
Classification | D - ICD-10: D59.0
- ICD-9-CM: 283
|
---|
Diseases of red blood cells (D50–69,74, 280–287) |
---|
↑ | |
---|
↓ | Anemia | Nutritional |
- Micro-: Iron-deficiency anemia
- Macro-: Megaloblastic anemia
|
---|
Hemolytic (mostly normo-) | Hereditary |
- enzymopathy: Glucose-6-phosphate dehydrogenase deficiency
- glycolysis
- pyruvate kinase deficiency
- triosephosphate isomerase deficiency
- hexokinase deficiency
- hemoglobinopathy: Thalassemia
- Sickle-cell disease/trait
- Hereditary persistence of fetal hemoglobin
- membrane: Hereditary spherocytosis
- Minkowski–Chauffard syndrome
- Hereditary elliptocytosis
- Southeast Asian ovalocytosis
- Hereditary stomatocytosis
|
---|
Acquired | AIHA |
- Warm autoimmune hemolytic anemia
- Cold agglutinin disease
- Donath–Landsteiner hemolytic anemia
- Paroxysmal cold hemoglobinuria
- Mixed autoimmune hemolytic anemia
|
---|
- membrane
- paroxysmal nocturnal hemoglobinuria
- Microangiopathic hemolytic anemia
- Thrombotic microangiopathy
- Hemolytic-uremic syndrome
- Drug-induced autoimmune
- Drug-induced nonautoimmune
- Hemolytic disease of the newborn
|
---|
|
---|
Aplastic (mostly normo-) |
Hereditary: Fanconi anemia
Diamond–Blackfan anemia
- Acquired: Pure red cell aplasia
- Sideroblastic anemia
- Myelophthisic
|
---|
Blood tests |
- Mean corpuscular volume
- normocytic
- microcytic
- macrocytic
- Mean corpuscular hemoglobin concentration
|
---|
|
---|
Other |
- Methemoglobinemia
- Sulfhemoglobinemia
- Reticulocytopenia
|
---|
|
---|
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 自己免疫性溶血性貧血の病因:温暖凝集素と薬剤pathogenesis of autoimmune hemolytic anemia warm agglutinins and drugs [show details]
…spherocyte , which is ultimately destroyed in the spleen. Drug-induced AIHA – A number of drugs elicit immune reactions that result in hemolysis The drug may alter antigens on the red cell, resulting in the …
- 2. 薬物および毒素による溶血性貧血hemolytic anemia due to drugs and toxins [show details]
… diminishes rapidly, the rate depending upon the clearance of the drug. The direct Coombs test in the immune complex type of drug-induced AIHA is usually positive with anti-C3 antisera but negative with anti-IgG …
- 3. 小児の自己免疫性溶血性貧血:分類、臨床的特徴、診断autoimmune hemolytic anemia in children classification clinical features and diagnosis [show details]
… pneumoniae and Epstein-Barr virus (in patients with cold AIHA only) Review of the patient medications to identify potential drugs that may induce AIHA Determination of the antigenic specificity of erythrocyte …
- 4. 小児の自己免疫性溶血性貧血:治療と転帰autoimmune hemolytic anemia in children treatment and outcome [show details]
…autoimmune disease-induced AIHA may benefit from earlier initiation of rituximab therapy. In patients with suspected drug-induced AIHA , it is imperative that the offending drug be discontinued. In …
- 5. 寒冷凝集素症cold agglutinin disease [show details]
…anemia include warm AIHA, drug-induced hemolytic anemia, hemolytic transfusion reactions (HTRs), and paroxysmal cold hemoglobinuria (PCH). Warm AIHA and drug-induced hemolytic anemia – Warm AIHA is the most …
English Journal
- Management of Select Thrombocytopenias.
- , V V, T T, T T, .
- AACN advanced critical care. 2019 ;30(2)165-180.
- Evaluating, diagnosing, and managing patients with consumptive thrombocytopenia is challenging because of the overlapping nature of many of the diseases that reduce platelet counts. Immune thrombocytopenia (and its variations), drug-induced immune thrombocytopenia, and heparin-induced thrombocytopen
- PMID 31151947
- Artesunate-Induced Severe Autoimmune Hemolytic Anemia in Complicated Malaria.
- Singh S, Singh SK, Tentu AK, Kumar A, Shahbabu B, Singh V, Singh N.
- Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine. 2018 Oct;22(10)753-756.
- Autoimmune hemolytic anemia (AIHA) is a very rare cause of anemia in a case of malaria and drug-induced AIHA is even rarer. A 50-year old patient with a history of fever for 8 days was diagnosed with a case of complicated malaria with mixed infection having initial parasite index of 45%. He showed g
- PMID 30405291
- A patient with oxaliplatin immune-induced syndrome (OIIS) who also developed leucovorin and palonosetron-associated thrombocytopenia.
- Curtis SA, Curtis BR, Lee AI, Hendrickson JE, Lacy J, Podoltsev NA.
- Hematology (Amsterdam, Netherlands). 2018 Aug;23(7)429-432.
- We report a case of an 83 year old man who developed oxaliplatin immune-induced syndrome (OIIS) after his 19th cycle of FOLFOX (5FU, leucovorin, oxaliplatin). When oxaliplatin was omitted from his next cycle of chemotherapy he continues to show signs of drug-induced immune thrombocytopenia (DITP) an
- PMID 29281948
Japanese Journal
- Levofloxacinによると推測される薬剤性免疫性溶血性貧血の1例
- 土手内 靖,尾崎 牧子,西山 記子,長谷部 淳,谷松 智子,西山 政孝
- 医学検査 64(1), 60-65, 2015
- … 43病日に薬剤リンパ球刺激試験を施行したところ,LVFXに対し陽性であり,臨床経過と併せ,本例はLVFXによる薬剤性免疫性溶血性貧血(Drug-induced immune hemolytic anemia:DIIHA)と推測された。 …
- NAID 130005057089
- 混合型自己免疫性溶血性貧血をともなうEvans症候群の1症例
- 天本 貴広,岡村 孝,佐川 公矯,江頭 弘一,川野 洋之,東谷 孝徳,石丸 健,佐藤 進一郎,奥 英二郎,今村 理恵,中島 収
- 日本輸血細胞治療学会誌 58(4), 539-546, 2012
- 自己免疫性溶血性貧血(AIHA)は赤血球に対する自己抗体の産生を特徴とする.AIHAは,抗体が赤血球と最もよく反応する至適温度により分類され,その分類には,温式AIHA,冷式AIHA,発作性寒冷血色素尿症,混合型AIHA,そして薬剤依存性AIHAなども含まれる.<br> 今回,我々は混合型AIHAによる急速で重篤な溶血をともなうEvans症候群を経験し,赤血球に対する自己抗体解析を行っ …
- NAID 130004542671
- 薬剤起因性と考えられる2度の無顆粒球症を発症した血管免疫芽球性T細胞リンパ腫
- 井上 大地,木村 隆治,下地 園子 [他],森 美奈子,永井 雄也,田端 淑恵,倉田 雅之,松下 章子,永井 謙一,丸岡 隼人,山下 映子,高橋 隆幸
- 臨床血液 50(2), 87-91, 2009-02-28
- 症例は73歳男性。2007年7月に発熱,紅斑,白血球減少のため入院。薬剤服用歴,白血球数1,400/μ<i>l</i>, 好中球0%, 骨髄顆粒球系細胞の著減より薬剤起因性無顆粒球症と考えられた。G-CSF製剤の投与により好中球数は正常化したが,表在リンパ節腫脹を認め,皮疹,発熱も持続し,自己免疫性溶血性貧血や2度目の薬剤性と考えられる無顆粒球症を来たしたため,リンパ …
- NAID 10024958956
Related Links
- Drug-induced immune hemolytic anemia is a blood disorder that occurs when a medicine triggers the body's defense (immune) system to attack its own red blood cells. This causes red blood cells to break
- Guidelines on the management of drug‐induced immune and secondary autoimmune, haemolytic anaemia Quentin A. Hill http://orcid.org/0000-0002-0627-4358 Department of Haematology, Leeds Teaching Hospitals, Leeds, UK ...
- Drug-induced immune hemolytic anemia (DIIHA) is an extremely rare blood disorder. The condition is estimated to occur in one in every one million people. It occurs when a medication you are taking causes your body’s ...
★リンクテーブル★
[★]
- 英
- drug-induced autoimmune hemolytic anemia
- 関
- 自己免疫性溶血性貧血
機序 (WCH.1175)
- 薬物と特定の型の赤血球上に存在する抗原が新しい抗原を作り、これを自己抗体が認識する
- 薬単体や、薬と特定の型を持たない赤血球にたいしては自己抗体を作らない(特定の型の赤血球とはI,Rh)。
- autoimmune mechanism: α-methyldopa type
- nonimmunologic protein adsorption mechanism
- multiple mechanism
[★]
- 英
- drug-induced acute hemolysis
- 関
- 薬剤性溶血性貧血 drug-induced hemolytic anemia、薬物誘発性自己免疫性溶血性貧血 drug-induced autoimmune hemolytic anemia
[★]
- 誘発する、誘導する、誘起する、導入する、引き起こす
- 関
- cause、challenge、derivation、elicit、elicitation、evocation、evoke、guidance、induction、inductive、introduce、introduction、precipitate、provocation、provoke、spark
[★]
-
- hypercalcaemia induced pancreatitis 高カルシウム血症による膵炎
[★]
- 関
- haemolysis、haemolytic、hemolysis、hemolyze
[★]
- 同
- drugs